You are on page 1of 17

Archives of Microbiology (2020) 202:935–951

https://doi.org/10.1007/s00203-019-01796-9

MINI-REVIEW

Current approaches and trends in the production of microbial


cellulases using residual lignocellulosic biomass: a bibliometric
analysis of the last 10 years
Joyce Cristina Gonçalvez Roth1   · Michele Hoeltz1   · Lisianne Brittes Benitez1 

Received: 20 August 2019 / Revised: 19 November 2019 / Accepted: 15 December 2019 / Published online: 11 January 2020
© Springer-Verlag GmbH Germany, part of Springer Nature 2020

Abstract
Considering the potential use of lignocellulosic biomass residues in microbial cultures to produce cellulases, the objective of
this research was to investigate trends and discussions regarding scientific research conducted in this field through a biblio-
metric and scientometric analysis. Using the Elsevier Scopus database and VOSviewer software, scientific papers published
between 2007 and 2018 were investigated. The results showed that the production of cellulases is related to obtaining xyla-
nases and glucose. Obtaining of bioethanol and determining cellulolytic and xylanase activities were the relevant indicators
for the use of these enzymes. China, India and Brazil are countries with a high number of publications in this field, most
likely due to investments made between 2015 and 2017. This analysis showed that research on the use of lignocellulosic
residues is focused on obtaining biofuels through enzymatic hydrolysis.

Keywords  Bibliometry · Biofuels · Biomass · Microbial cellulase

Introduction Cellulases are defined as multienzyme complexes formed


by three main components, endo-1,4-β-d-glucanase (EC
Cellulose is the most abundant natural biological renewable 3.2.1.4), exoglucanase/exo-cellobiohydrolase (EC 3.2.1.91)
resource, and the production of bioproducts and bioenergy and β-glucosidase (EC 3.2.1.21), which synergistically
using waste from this natural material is fundamental to hydrolyze the cellulose polymer into glucose monomers.
meeting the demand for sustainable processes. Cellulose, Cellulases are considered bioproducts with great economic
hemicellulose and lignin are the main constituents of lig- appeal due to various industrial applications, such as deter-
nocellulosic materials, and their availability for use in bio- gent, textile, feed and food, paper and biofuel industries
processes is important to enabling its use, since cellulose (Zhang et al. 2006; Juturu and Wu 2014; Singhania et al.
and hemicellulose are found in a stable crystalline struc- 2017).
ture (Iranmahboob et al. 2002; Kumar et al. 2009; Valencia Microbial cellulases were initially recognized for their
and Chambergo 2013; Thomas et al. 2016; Rodrigues et al. ability to deteriorate cellulosic materials used in American
2017). camps during World War II. In 1950, the microorganism, the
Trichoderma viride fungus, that caused these deteriorations
and the enzymes excreted by it were known to degrade cel-
Communicated by Erko Stackebrandt . lulose. This was demonstrated in experiments conducted by
Dr. Elwyn T. Reese and Dr. Mary Mandel (White et al. 1950;
* Lisianne Brittes Benitez Reese 1956). Many advances have been made in recent dec-
lisianne@unisc.com
ades, and the use of microbial cellulases in industrial pro-
Joyce Cristina Gonçalvez Roth cesses has rapidly been demonstrated.
joyce_goncalvez@hotmail.com
Many investments have been made to optimize the pro-
Michele Hoeltz duction of microbial cellulases from residual lignocellu-
hoeltz@unisc.com losic biomass in the form of powders, bagasse, shells, brans
1
Universidade de Santa Cruz do Sul., Av. Independência, and residual cakes. These residues are available and suffi-
2293, Universitário, Santa Cruz do Sul, RS, Brazil ciently abundant in all parts of the world, and burning these

13
Vol.:(0123456789)

936 Archives of Microbiology (2020) 202:935–951

residues, which is the most common processing method, in microbiological processes, there is a lack of systematic
compromises the environmental quality of ecosystems. studies that indicate the evolution of this area of study. Con-
Therefore, the processing of residual lignocellulosic bio- sidering the potential use of lignocellulosic biomass residues
mass, in addition to being an adequate environmental alter- in microbial cultures to produce microbial cellulases, the
native, can be economically attractive for the bioproducts objective of this research was to reveal relevant aspects by
that it can create (Yang et al. 2006; El-Haggar 2007; Thomas the analysis of the temporal evolution and discuss the trends
et al. 2016). of the scientific research conducted in this field through a
Bibliometrics is a tool designed to evaluate the scientific bibliometric and scientometric analysis.
production of researchers in several fields. Scientometrics
combined with bibliometrics enables an evolutionary quanti-
tative evaluation of the most diverse scientific fields and can Methodology
be applied to identify emerging areas of study. Scientomet-
rics performs a measurement of scientific communication, This research focused on the main aspects involving the use
while bibliometrics addresses more general information pro- of agroindustrial residues to produce microbial cellulases.
cesses (Da Silva and Pires Bianchi 2001; Patra et al. 2006). Initially, a general search was conducted in the Scopus and
The use of isolated bibliometric indicators is not an Web of Science databases for the representative occurrence
appropriate interpretation of data. It is necessary to jointly of the number of publications provided by the respective
associate other metrics, such as Scientometrics, to provide databases when using the terms "cellulase," "microorgan-
a realistic assessment of the scientific area of interest (Da isms" and "fermentation", applied to scientific articles from
Silva and Pires Bianchi 2001). However, "scientific activity 2007 to 2017. This first search (Search 1) considered the
cannot be reduced to the production, circulation, and con- presence of these terms in the title, abstract and keywords
sumption of periodicals, much less confusing quantitative of the article.
article growth with the cognitive development of science" The search in the Scopus database yielded 333 articles,
(Santos and Kobashi 2009). while the Web of Science database yielded 125 articles.
Bibliometric and scientometric analyses began in the This result was expected because of the wider range of jour-
1960s but only came to be seen as tools of scientific anal- nals included in the Scopus database (Falagas et al. 2008).
ysis in the 1970s (Patra et al. 2006), the same period in Although the databases mentioned differ in terms of scope,
which discussions about environmental problems from the volume of data and different coverage policies, the results
production and nontreatment of waste began to gain trac- and impacts of the countries are correlated; that is, the cor-
tion in the scientific community. The Stockholm Confer- relations between the two databases in terms of the number
ence (1972), which resulted in the publication of the report of citations from countries and their respective classifica-
"Limits to Growth" by the Club of Rome and the creation of tions are similar (Archambault et al. 2009). Therefore, the
the "United Nations Environment Program (UNEP)," rein- Elsevier Scopus database was chosen to perform the biblio-
forced the concerns about the adverse environmental effects metric analysis.
(Pelizer et al. 2007). Afterwards, a systematic review of the content of arti-
The main tools used in bibliometric studies are the Web cles was conducted by reading the abstracts, following the
of Science, Scopus and Google Scholar Metrics databases PRISMA protocol (Preferred Reporting Items for Systematic
(Table 1). These databases include different data and use dif- Reviews and Meta-Analysis), which shows the flow of infor-
ferent metric indicators that are very useful in bibliometric mation with the different applied phases of the systematic
research and can be used to determine the changes to areas review (Fig. 1).
of study over time (Lopes et al. 2012). For the bibliometric analysis, VOSviewer software, ver-
Although there is an increasing number of scientific stud- sion 1.6.6 was used with 253 exported articles included
ies addressing the incorporation of agroindustrial residues by the PRISMA protocol in the CSV format. This analysis

Table 1  Details of the main databases used in bibliometric studies. Source: Lopes et al. (2012), Elsevier (2017), Halevi et al. (2017)
Database Basis used to evaluate indexed journals Access Time of coverage Indexed material
(citations)

Web of Science (Thomson Reuters) Journal Citation Reports (JCR) Limited Since 1898 Scholarly literature
Scopus (Elsevier) Scimago Journal and Country Rank (SJR) Limited Since 1970 Scholarly literature
Google Scholar Metrics (Google) Lack of accurate indexing information Free Since 2004 All output regard-
less of peer-
review

13
Archives of Microbiology (2020) 202:935–951 937

Fig. 1  Application of the PRISMA protocol to the 333 articles ini- Fig. 2  Application of the PRISMA protocol to the 94 articles initially
tially selected in the Elsevier Scopus database (Research 1) per- selected in the Elsevier Scopus database obtained by the query of the
formed on January 20, 2018 terms "cellulase production" and "microorganism" (Research 2) lim-
ited to the period from 2007 to 2018

used a binary counting method where the keywords were grouped according to similarity or interrelationship. The
present in both the title and the abstract of the included scientometric analysis included information provided by
articles. To include the formation of clusters, the criterion the Scopus database, which allowed the graphical analysis
of 12 minimum occurrences was adopted, resulting in 72 of the articles in relation to the year of publication, coun-
terms that were then grouped according to similarity or try of origin, affiliation and scientific areas of study. The
interrelationship. articles that were excluded after applying the PRISMA
Due to the results obtained in the first analysis, it was protocol were manually removed for the correct interpreta-
decided to perform two other searches to individualize the tion of the results that were obtained graphically.
analysis on the microbial production of cellulases and their
application in the period from 2007 to 2018. Afterwards,
the results of both searches were submitted to the PRISMA
protocol for the selection and inclusion of articles.
Regarding the terms "cellulase production" and "micro-
organism" (Search 2), the database found 94 articles whose
key words were present in the title, abstract or keywords
from 2007 to September 2018. Of these 94 articles, 59 were
excluded because they were revisions, were focused on the
application of microbial cellulases in fermentative processes
or did not present a direct relationship with microbial cellu-
lases (Fig. 2). For the terms "cellulase" and "potential appli-
cation" (Search 3), the database found 158 articles whose
key words were present in the title, abstract or keywords
from 2007 to September 2018. After the abstracts were read,
56 articles were excluded, according to Fig. 3.
For these new bibliometric mappings, a binary count-
ing method was used, which included the presence of the
terms searched in the title, abstract or keywords of the
Fig. 3  Application of the PRISMA protocol to the 158 articles ini-
article. The formation of the clusters for the two analyses
tially selected in the Elsevier Scopus database obtained by the query
was based on the criterion of 5 minimum occurrences, for the terms "cellulase" and "potential application" (Research 3) lim-
resulting in 48 and 46 terms, respectively, which were then ited to the period from 2007 to 2018

13

938 Archives of Microbiology (2020) 202:935–951

Results and discussion a new search. For the updated search, microbial production
and the potential applications of cellulase were individually
Bibliometry investigated (Research 2 and 3).
In Fig. 5, the new bibliographic mapping indicated by
The clusters obtained in Research 1 show the different the software can be observed and allows a clear and more
approaches identified by the abstracts of the articles, as fol- precise analysis of the microbial production of cellulase. In
lows: (i) the use of the cellulase enzyme to obtain bioethanol this search, we were able to highlight issues related to the
and the different processes used for this purpose, such as microbial production of cellulases, such as the bioprocesses,
the treatment of lignocellulosic biomass and saccharification substrates and microorganisms that were used as well as
(red cluster), and (ii) production of the cellulase enzyme the methodologies used for the quantification of cellulolytic
from microbial cultures (green and blue clusters) (Fig. 4). enzymatic activities.
The enhancement to the red cluster is expected because of The clusters that were generated demonstrated specific
the popularity of cellulases in 2005 due to the production of methodologies for the determination of microbial cellulo-
lignocellulosic ethanol through enzymatic hydrolysis (Sin- lytic activities from glucose generated by the degradation of
ghania et al. 2017). However, the use of cellulases through cellulose present in the lignocellulosic biomass (green clus-
microbial cultures is not focused on bioethanol alone, even ter) and two other groups are shown that are closely related
though this is currently the most popular use of cellulases to the bioprocesses involved in the production of the cellulo-
(Singhania et al. 2017). The investigation of aspects that are lytic/hemicellulolytic enzyme complex, which is attributed
intrinsic to the bioprocess of obtaining cellulase were lim- to the presence of xylanase (blue and red clusters). Although
ited in the graphical interpretation generated by the software. there was a difference between the groups generated by the
The term "fermentation" used in the research perme- software, the analysis was performed considering the blue
ates the 3 clusters because the fermentative processes can and red clusters as a single group due to their similarities.
be observed from the perspective of microbial production, The main link between the clusters is due to the term
through bioprocesses, correlating closely with the blue and "enzyme production", whose influence of the occurrences
green clusters, and also in the applied industrial perspective, (number of relations of the term to term) is 23% (result pro-
by the use of totally or partially isolated enzymes, focus- vided by the software). This connection between the groups
ing on the hydrolysis of lignocellulosic materials. There- is important and was expected, since the analysis conducted
fore, the duality observed by the above-generated clusters on the included articles was focused on this theme, which is
yielded incorrect inferences regarding the arguments and closely related to bioprocessing with xylanases and glucose
trends identified by bibliometric mapping, which suggested (sugar).

Fig. 4  Clusters formed by keywords used in the bibliometric analysis. The dimensions of the circles represent the occurrences of the terms in the
analysis of the 253 articles included in the bibliometric analysis (Research 1)

13
Archives of Microbiology (2020) 202:935–951 939

Fig. 5  Clusters formed by the


keywords "cellulase production"
and "cellulase" used in Research
2. The dimensions of the circles
represent the occurrences of the
terms in the analysis of the 94
articles included in the biblio-
metric analysis

In addition, the determination of enzymatic activities highly active enzymes at moderate temperatures are more
by the analytical methods routinely used is based on the relevant. Many commercial products can be obtained from
quantification of glucose content in solution resulting from xylan, such as xylitol, ethanol, lactic acid and furfural. The
carbohydrate hydrolysis (e.g., cellulose) by the action of the recent challenge in the use of xylanases is the development
enzyme. Thus, a higher amount of glucose indirectly reflects of an economical process that solubilizes the lignocellulosic
higher enzymatic microbial productivity, which reflects the material and allows its use as a renewable source of energy, a
interaction between the terms of the blue and green cluster. supplement in animal feed and for the manufacture of bever-
The distance between the green and blue clusters could ages, food, textiles and industrial pulp and paper (Shallom
be explained by the differences in the performance of enzy- and Shoham 2003; Collins et al. 2005; Juturu and Wu 2014;
matic complexes to cellulose and hemicellulose polymers. Bajpai 2014a).
Cellulase activity in fermentation processes can be deter- This multiplicity of xylan is justified by the nontoxic and
mined by specific methodologies for the multienzyme com- biocompatible properties inherent to the molecule, provid-
plex cellulase, including endo-1,4-beta-d-glucanase (EC ing many biotechnological applications by various indus-
3.2.1.4), exoglucanase/exo-cellobiohydrolase (EC 3.2. 1.91) tries (Bajpai 2014b; Petzold-Welcke et al. 2014; Naidu et al.
and beta-glucosidase (EC 3.2.1.21). These components act 2018). The microorganisms that are most prominently used
synergistically for complete hydrolysis of the cellulose poly- for the extracellular production of xylanases include Asper-
mer in glucose monomers (Singhania et al. 2017). gillus niger and Trichoderma viride fungi in addition to the
Hemicellulolytic activity is especially associated with fungal genera Phanerochaetes, Chytridiomycetes, Rumino-
disruption of the xylan polymer, which represents the main coccus, and bacterial genera Streptomyces, Clostridium and
polymer of hemicellulose. Xylans are second to cellulose Bacillus, as well the phylum Fibrobacteres (Shallom and
with respect to constituency and abundancy of the polysac- Shoham 2003; Collins et al. 2005; Gonçalves et al. 2005).
charides available in lignocellulosic biomass. Currently, The selection of microorganisms, fungi or bacteria, with
industrial xylanases are mesophilic and neutrophilic. Sta- a favorable metabolic capacity, combined with the optimiza-
ble enzymes under extreme environmental conditions, such tion of biomass conversion processes are crucial, because the
as temperature and pH, could advance the bioprocesses of microbial enzymes are influenced by a variety of nutritional
lignocellulosic biomass conversion, especially with respect and physiological factors, which explains the proximity of
to hemicellulose hydrolysis (Collins et al. 2005; Gonçalves the blue and red clusters (Fig. 5). Only a few microorgan-
et al. 2005; Gonçalves et al. 2015). isms can address the obstacle posed by lignin, which allows
For biotechnological applications, stable xylanases in the effective action of hemicellulases and cellulases and the
specific temperature and pH ranges may be required. For subsequent use of vegetable polysaccharides by other micro-
example, in the paper industry, stable enzymes in thermoal- organisms. This process is characterized as an oxidative pro-
kaliphilic conditions are useful, while in the food industry, cess that does not directly depend on the culture conditions

13

940 Archives of Microbiology (2020) 202:935–951

of microorganisms that are able to degrade lignin, which is Smaller environmental impacts associated with pollution
considered an important factor in the industrial uses of lig- are caused by enzymatic hydrolysis and saccharification of
nocellulosic biomass to obtain bioproducts such as bioetha- biomass to fermentable sugars. The ideal environmental
nol and other materials based on cellulose (Kirk and Farrell conditions for the activity of these enzymes generally occur
1987; Lynd et al. 2002; Ruiz‐Dueñas and Martínez 2009; under mild environmental conditions, which include tem-
Thomas et al. 2018). perature, pressure and pH, compared to chemical processes
Lignin is enzymatically hydrolyzed (by laccases among involving the hydrolysis of pretreated biomass. Enzymatic
other enzymes), especially by fungi under solid substrate hydrolysis also reduces energy expenditure, the amount of
fermentation (SSF). SSF is more applicable and simple materials used to make equipment and the occurrence of
for hydrolyzing lignocellulosic biomass because insoluble toxic substances, such as acetic acid, furfural and hydroxy-
materials act by supporting microorganisms that also use methylfurfural, when fungi and bacteria are used to pro-
it as a source of nutrients. Water is generally complexed duce cellulase (Iranmahboob et al. 2002; Kumar et al. 2009;
in the solid matrix of the substrate, and in the presence or Juturu and Wu 2014; Jung et al. 2015; Singhania et al. 2017;
absence of free water, the risk of contamination is reduced. Naidu et al. 2018).
The moisture content and particle size are important when Agroindustrial wastes are abundant and available in all
agroindustrial residues are used because these factors can parts of the world, and in addition to being an adequate envi-
limit SSF (Malherbe and Cloete 2002; Couto and Sanromán ronmental alternative, their processing for the production
2006; Yang et al. 2006; Castro and Pereira Jr 2010; Behera of cellulases is advantageous from an economic point of
and Ray 2016; Ergun and Urek 2017). view. Dhabhai et al. (2013) demonstrated that thermal pre-
Solid substrate fermentation provides higher yields of treatment and acid hydrolysis were able to increase surface
enzymatic production compared to submerged fermentation area, spore volume and reduce crystallinity, allowing a better
(SmF) in addition to lower operating costs. However, it is use of biomass and obtaining bioproducts. However, effi-
estimated that 80% of the worldwide production of hemi- cient conversion processes for residual biomass need to be
cellulolytic enzymes is obtained by SmF (Polizeli et al. ensured through research and development of new technolo-
2005; Couto and Sanromán 2006; Yang et al. 2006; Cas- gies that can transform the cellulase market and improve the
tro and Pereira Jr 2010; Behera and Ray 2016; Ergun and environmental quality of the systems (Sun and Cheng 2002;
Urek 2017) as confirmed by the presence and interaction of Zhang and Lynd 2004; Zhang et al. 2006; Kumar et al. 2009;
the search terms "submerged fermentation", "xylanase" and Thomas et al. 2016; Rodrigues et al. 2017).
"enzyme production”, as shown in the blue cluster. Efficient and economically feasible processes for the
Fungi influence the red cluster possibly due to their conversion of residual biomass to cellulases can be ensured
prominent use in crops that target the industrial production by the following approaches: (i) improving efficiency in the
of cellulases. Most fungi are endo- and exo-cellulase pro- production of enzymes using genetically modified organ-
ducers, and the combinations of these enzymes may lead isms, (ii) using inexpensive raw materials, (iii) engineering
to a synergistic increase in cellulose degradation activity, immobilization and enzymatic recycling approaches, and
facilitating both internal and external cleavage of cellulose (iv) increasing the saccharification capacity of the substrate
molecules (Moraïs et al. 2010; Sharma and Yazdani 2016). using enzymatic cocktails that are capable of acting on a
Exoglucanases directly act on the substrate by releasing cel- wide variety of substrates. For this purpose, various cellulo-
lobiose or glucose from the polymer, thus destratifying the lytic enzymes may be used in combination, including ligno-
fibers and physically breaking down the substrate, which cellulases, such as xylanases (Zhang and Lynd 2004; Zhang
maximizes cellulose hydrolysis. et al. 2006; Behera and Ray 2016; Thomas et al. 2016; Ergun
Bacteria, which mostly only produce endoglucanases, are and Urek 2017; Sóti et al. 2018).
robust and versatile enzymatic sources because they present Genes that are responsible for the production of cel-
high growth rates and multienzymatic complexes (Asgher lulases have been isolated from Penicillium oxalicum and
et al. 2007). The majority of bacterial cellulases originate showed great importance in the production of cellulases
from the Bacillus genus (Sharma and Yazdani 2016), as and xylanases (Ye et al. 2017). Similarly, a mutant strain of
shown by the red cluster. Trichoderma reesei, whose hydrolysis efficiency of alkali
For fungi or bacteria, chemical and physical pretreat- pretreated corn straw reached approximately 99% of glu-
ments may be required to provide cellulose and hemicellu- cose conversion, produced more cellulases compared to the
lose. These pretreatments increase the porosity of vegetable native strain (Zhang et al. 2017). Tenth generation spores
fibers and reduce its crystallinity, which affects the avail- of the Talaromyces verruculosus fungus that were obtained
able surface area. Sequentially, biomass is processed into by UV radiation at a wavelength of 254 nm were also able
constitutive sugar monomers through a hydrolysis reaction to increase the production of endoglucanases (Jain and
(Mcmillan 1994; Kumar et al. 2009; Thomas et al. 2016). Agrawal 2018).

13
Archives of Microbiology (2020) 202:935–951 941

Corn hydrolysates have been used in ethanol production Supplementation of cellulases with xylanase from
by implementing a multienzyme system with a strain of the Aspergillus sp. improved the saccharification of rice straw
genus Gracilibacillus, which reached an efficiency above pretreated with alkali by 25% compared to the use of xyla-
50% for the production of bioethanol (Yu and Li 2015). nase-free cellulases. Xylanase was produced by solid-state
Bagasse, corn cob and rice straw residues (all submitted to fermentation after 96 h of incubation, 80% substrate mois-
pretreatment) have been used by Bacillus licheniformis for ture, pH 4.8 and a temperature of 25 °C using a carbon or
the evaluation of cellulase production by an experimental nitrogen source for wheat bran and yeast extract, respectively
design (Plackett–Burman), which showed that the addi- (Thomas et al. 2016).
tion of Tween-20 and a temperature of 43.35 °C were the Since 2005, microbial cellulases have been very popu-
optimal conditions for maximum productivity (Shajahan lar due to the resurgence of bioethanol production as an
et al. 2017). alternative to fossil fuels. There are other routes that allow
Additionally, the optimal experimental conditions for the conversion of lignocellulosic biomass into ethanol, but
the production of cellulases by Bacillus subtilis MUS1 have the enzyme has become popular due to its sustainability. In
been evaluated, and the optimization of production was per- addition, recycling of residual biomass can promote local
formed by the Plackett–Burman delineation, which demon- economies while eliminating potential competition with
strated that carboxymethylcellulose (CMC), yeast extract, crops for food supplies and reducing processing costs and
NaCl, pH, M ­ gSO4 and N ­ aNO3 were the most significant disposal of generated waste. Additionally, the production
factors that affected the production and resulted in increasing cost of cellulase still represents a significant fraction of the
the enzymatic activity approximately three-fold compared to production cost of bioethanol (Singhania et al. 2017; Gomes
the nonoptimized condition (Screena and Sebastian 2018). et al. 2018).
Bacillus sp. was used for extracellular enzymatic pro- In Search 3, three clusters were generated (Fig. 6) that
duction (endoglucanases, total cellulase and β-glycosidase) evidenced the following:
from solid residues of corn grain and was sensitive to all
antibiotics tested, indicating that it is safe for the production (i) the use of cellulase to obtain biofuels, specifically
of cellulases (Thomas et al. 2018). Another strain of Bacil- bioethanol, obtained through the pretreatment of lig-
lus sp. was also evaluated for the processing of sugarcane nocellulosic biomass by enzymatic hydrolysis allows
bagasse and corn maceration liquor to produce avicellase for the removal of lignin and hemicellulose for sac-
and CMCase. Maximum production was reached after 120 charification and obtaining fermentable sugars, such
and 168 h, respectively, at 70 °C. The potential applications as glucose, bioethanol or second generation ethanol
of these enzymes by the detergent industry has been evalu- (E2G) (red cluster);
ated by investigating residual cellulase activity after contact (ii) different methods for determining the enzymatic
with detergent solutions (Ladeira et al. 2015). activity of the cellulolytic complex and the consump-
The production of cellulases can greatly contribute to the tion of substrates for cellulases for this quantifica-
viability of second -generation ethanol by increasing the tion are closely associated with the terms "avicel",
yield using fermented hydrolysates of sugarcane bagasse. "cellobiose", "glucosidase" and "CMCase" in addi-
Yields higher than 11% were obtained when solid fermenta- tion to the importance of fungi and the use of crude
tion was used followed by submersion (sequential fermenta- enzymes for the production of bioethanol, since fungi
tion) (Cunha et al. 2017). are more adapted to fermentative conditions (such as
Rice straw has been shown to be an interesting substrate acidity) (green cluster); and
for cellulase production because biomass pretreatment is (iii) the use of microbial cellulases (associated with
important for the improvement of T. reesei enzymatic activ- the term bacillus) to obtain fermentable sugars or
ity, and the combined use of the enzyme complexes from the treatment of lignocellulosic biomass to obtain
both strains significantly increased enzymatic activity (Kogo xylanase for industrial use, either by the bioethanol
et al. 2017). industry or the paper industry.
Enzymatic immobilization has been shown to increase
the hydrolytic efficiency of plant and fruit residues and the The link between the three groups that is clearly formed
recovery of anthocyanins (pigments) due to the stability of is due to the optimization of microbial processes for the
immobilized cellulases, which are maintained twice as long production of cellulases and their applications. Although
as free enzymes (Yuan et al. 2016). Cellulase immobiliza- references are not made to the application of microbial cellu-
tion was also shown to be an interesting technique due to lases in the search of articles in the database, the mapping of
increased stability and reduction of denaturation when com- the data was able to determine this connection by indicating
pared to free enzyme when employing metal–organic frame- close interrelations with the main and current trends for the
works to immobilize enzyme cellulose (Ahmed et al. 2018). use of cellulases in the field of biofuels.

13

942 Archives of Microbiology (2020) 202:935–951

Fig. 6  Clusters formed using the keywords "cellulase" and "potential application" in Research 3, where the dimensions of the circles under each
term represent the influence of the term in relation with the other terms

A considerable distance between the terms "fungi" and processes (Motta et al. 2013; Feng et al. 2016; Singhania
"xylanase" is observed, which, according to Motta et al. et al. 2017; Akram et al. 2018; Chang et al. 2018).
(2013) could be justified by the low biomass yield in fermen- In the red cluster, which suggests the industrial tendency
tative processes in which the use of agitation to homogenize of applying cellulases, terms are closely related to the pro-
the fermented medium may negatively affect the develop- cess of obtaining biofuels. These terms are related to the
ment of fungal biomass, especially by hyphae rupture. How- hydrolysis of lignocellulose to glucose and involving the
ever, submerged fermentation processes are considered opti- degradation of lignin to cellulose and hemicellulose release.
mal for the enzymatic hydrolysis of lignocellulosic material Microorganisms, especially fungi, have enzymatic abilities
whose yield is easily affected by fluctuations in fermentation capable of degrading the plant cell wall through a synergis-
conditions, better controlled when conducted in a submerged tic action that leads to glucose release (Akram et al. 2018;
mode (De Souza 2013; Akram et al. 2018). Singhania et al. 2017). The connection between the terms
In the green cluster, most commercial cellulases are present in this cluster proves that the main route to obtain
obtained through the use of filamentous fungi, which ethanol is through the use of bioprocesses, in which sugars
explains the composition of the group. In this cluster there is are converted into ethanol through the performance of yeasts
the substrate "avicel", industrially used to induce the produc- (Saccharomyces cerevisiae, for example) via saccharifica-
tion of cellulases, the determination of enzymatic activity by tion. A sustainable option for this process and for the global
"CMCase" and the products of cellulose hydrolysis, such as fuel market has been made possible by obtaining glucose via
the dimer "cellobiose". The enzymes "glycosidases", which residual biomass lignocellulosic (Souza 2012; Lopes et al.
act on the β-1,4-glycosidic bonds present in the linear chains 2016; Akram et al. 2018), referenced by the presence of the
of the d-glucose units in cellulose, stand out in the cluster. terms "pretreatment", " biofuel", ’’ ’biofuel production" and
β-Glucosidase is prominent in the production of lignocellu- "enzymatic hydrolysis".
losic ethanol, which is demonstrated by the proximity of this Pretreatment is an essential step for obtaining biofuels,
term to "bioethanol". It is important to note that the ideal pH because only this way there is a rupture of the cellulose crys-
conditions for conducting the submerged fermentative pro- talline structure and breakdown of the matrix bound to hemi-
cess are perfectly suited for most industries, especially those cellulose and lignin, which increase the surface area and
of paper and cellulose, highlighted in the cluster. To obtain porosity of cellulose. This process however, represents an
xylanases is also observed applying submerged fermentation economic barrier to the expansion of biofuel production, yet

13
Archives of Microbiology (2020) 202:935–951 943

it is an important technological alternative for not compet- commercial scale. By 2009 several were E2G biofuel pilot
ing with food production, since it is obtained from residual and demonstration facilities especially in North America,
biomass (Mood et al. 2013), such as maize straw, highlighted Europe, Brazil and Asia (Nguyen et al 2017).
in the figure. E2G biofuels use a wide variety of non-food biomass and
Among the strategies to circumvent the barriers imposed can be derived from any lignocellulosic material. In addi-
by biomass pretreatment would be the genetic modification tion, they allow variable bioproducts that go beyond etha-
of plant cell walls, altering cellulose crystallinity, increasing nol to include biodiesel (Nguyen et al 2017; Hassan et al.
hemicellulose content and reducing lignin levels. For this, 2019). Specifically, cellulosic ethanol has been accounted
the selection of appropriate genes is a fundamental step, for worldwide as a renewable fuel since 2011, when in Fig. 7
reflecting directly and mainly on the relationships between there is a strong emphasis on the term "xylanase", "optimal
the terms "gene" (green cluster) "xylanase" (blue cluster) activity" related to enzymatic treatment of residual biomass
"pretreatment" and "biofuel" (red cluster) (Mood et  al. and obtaining ’’fermentable sugar".
2013). The use of lignocellulosic waste materials and low-value
The last 40 years have been marked by many scientific is expressed as a valuable approach to the reduction of pro-
and technological advances related to bioprocesses, contrib- duction costs and to encourage the use of ethanol as a biofuel
uting significantly to the evolution of the ethanol industry (de Souza 2013; Lopes et al. 2016) evidenced by the terms
in Brazil and worldwide (Lopes et al. 2016). In Fig. 7, it can "saccharification", "glucose" and "pretreatment" of bio-
be seen from the relevance of the terms that these scientific mass via "enzimatic hydrolisis", especially related to E2G
contributions allowed a better understanding and consolida- "biofuel". The term "corn stover" appears in the figure in a
tion of the processes associated with obtaining first genera- centralized position as it is considered the main bioethanol
tion (E1G) and recently second generation (E2G) ethanol. feedstock worldwide (Hassan et al. 2019). Environmentally
The first generation of biofuels proved potential for large- and economically viable energy sources support important
scale production of renewable fuels, especially through the global changes and the direction of innovation in renewable
use of corn and sugarcane. This great productive orientation biofuels is therefore of great importance for policy mak-
remained until 2015 with the stabilization of world produc- ers and investors, as well as to the scientific community
tion, with second-generation biofuels being produced on a through research and development. This is demonstrated by

Fig. 7  Relevance of the terms in the period from 2012 to 2017, which demonstrated the improvement of processes in the biofuel industry

13

944 Archives of Microbiology (2020) 202:935–951

the relevance of terms over the years (Fig. 7) and coincides technological and commercial interest in the area. The tech-
with the period of greater investment in renewable energy nologies employed to obtain lignocellulosic biofuels are
by developing countries (Fig. 8). considered emerging and consequently characterized by an
Investments made by developed countries increased sig- intense patent race (Toivanen and Novotny 2017). There is
nificantly starting in 2009 and reached the greatest level in a large volume of patent applications that were submitted
2011. After a significant reduction, the trend remained stable from 2010 to 2017, a period that coincides with periods of
between 2012 and 2015. From 2016 onwards, the level of major global investments, but this is much lower than the
investment declined, and in 2017, the rates were lower than number of scientific documents that were published in the
the year of the start of the survey (2007). For developing same period of time. This indicates that the research and
countries, investments continued to grow until 2016, when development of related technologies is still very small and
investments slightly decreased, followed by an increase in requires more investments (De Figueiredo et al. 2018).
the following year. Publications associated with the potential applications of
The difference between the investments made in 2017 by cellulases that indicate a growing trend in the area of biofu-
developed and developing countries comes mainly from the els correspond with the similar growing research trends in
solar energy market, which for developing countries rep- developing countries, whose origin of approximately 70%
resented an increase of 41% that same year. However, it is of articles is associated with countries such as China, India
interesting to note that global investments in research and and Brazil. Even with the reduced number of publications in
development in the biomass and waste sector were higher 2016, this trend continues to increase at levels above those
than in other sectors such as solar and wind energy (UNEP observed from 2007 to 2012. With regard to published
2018), directly reflecting the increase in publications in this papers, most representative countries are considered in
area in 2017. Solar and wind energy systems are among the development; therefore, an assessment that includes invest-
largest sources of renewable energy, however, there is a sig- ments in renewable energy in these countries is relevant.
nificant amount of work aimed at optimizing the use of other Considering the investments made by developing countries
renewable sources for power generation such as hydroelec- and carried out by these countries, investments continued to
tric, wind, geothermal, lignocellulosic biomass and biofuel increase in 2007, reaching their highest value in 2015. From
(Iqbal et al. 2014; Vohra et al. 2014, Banerjee et al. 2018, 2015, the investments made by developed countries were
Viviescas et al. 2019). sustained until 2017.
The great potential associated with lignocellulosic energy Global investments dropped by 37% in 2015, which
is directly associated with its availability and renewable was the most significant change observed from 2004 to
nature, which has fueled and continues to fuel a growing 2016 (UNEP 2018); however, this trend was not observed

Fig. 8  Publications related to the keywords “cellulase”, “microorganisms” and “fermentation”) used in the bibliometric analysis from 2007 to
2017. Source: Adapted from Elsevier (2017) and UNEP (2018)

13
Archives of Microbiology (2020) 202:935–951 945

for developing countries. China, India and Brazil alone agricultural territorial expansion, which can lead to side
accounted for more than 50% of the investments made in effects such as a decrease in food supply and a reduction
2017 by developing countries. It is observed that China is in forest areas. Therefore, second-generation biofuels may
the country that received in 2017, the largest global invest- be able to mitigate these effects and significantly improve
ments in renewable energy, and even though this total, bio- productivity, provided there is technological and economic
mass represents less than 1% of these investments, is still feasibility that can be aided by government interventions,
higher than the investments made by the other countries such as production subsidies or tax exemptions for cellulosic
considered (United States and European countries) in this ethanol (Feres 2010; Nyko et al. 2010; Paulova et al. 2015).
same sector (UNEP 2018). The predicted scenario for the Therefore, investments and incentives are necessary to
year 2050 indicates that a significant share of residual bio- meet a new and growing world energy demand attributed
mass will be used for biofuels in the transport fuel market. to cellulosic ethanol, which reflects the new positions of
Half of this production demand will be from countries such countries with respect to environmental policies and impacts
as China and India, which will supply approximately 20% the reduction of fossil fuels and the emission of greenhouse
of this need together (Eisentraut 2010). gases (GHG) and an increase in the supply of biofuels and
Another relevant issue to be considered concerns the its international trade.
logistics systems for the service of commercial plants that In addition to its use in the emerging biofuel industry,
would allow the transformation of economically competitive cellulases are also used in the textile, food and animal feed
E2G. This is the case in India, where the predominance of industries by improving nutritional quality and digestibility
small farms is predicted to increase the logistic complexity and as an industrial raw material that is used for obtain-
of residual lignocellulosic biomass processing (Eisentraut ing solvents and resins (Zhang et al. 2006; Sadhu and Maiti
2010; Hiloidhari et al. 2014). 2013). It is expected that in the coming years, global demand
In the case of Brazil, the already consolidated processes for enzymes will significantly increase due to the character-
of obtaining ethanol through maize or sugarcane should not istics that they contribute to the process, such as reduced
be replaced by cellulose ethanol due to its technical and waste of raw materials, high specificity and good biodegra-
economic feasibility for commercial production. Even with dability, which are characteristics that address recent global
numerous advantages, such as noncompetition with the food environmental concerns (Reetz 2010).
chain and especially the availability of raw material, cel-
lulosic ethanol is still only produced on a small scale, espe-
cially for units distributed in Europe (Feres 2010; Rainer Distribution of publications by country
et al. 2013; Paulova et al. 2015; Song et al. 2018).
The technologies that are used to produce ethanol are lim- Investments in research and technological innovation are
ited and reflects the exhaustion of efficiency in agricultural some of the limiting variables that affect the cellulase mar-
and industrial productivity, where the technology that is cur- ket, which have been observed in a number of scientific pub-
rently used for first generation ethanol (E1G) is very close lications in this area of study. The number of documents
to their theoretical limits. While the productivity increase included when considering microbial cellulase production
in E1G is limited to a few percentage units, productivity (Research 2) in the bibliometric analysis shows that coun-
through new conversion routes, such as residual biomass, tries such as India, China and Brazil have prominent posi-
is estimated at five-fold higher values (Nyko et al. 2010). tions, with 28%, 16% and 12% of the publications, respec-
The United States, Germany and Japan are considered tively. This can be explained by the industrial importance
world leaders in lignocellulosic biofuels, and large invest- of cellulase and its demand that is motivated by the biofuel
ments in research in this sector have been demonstrated. industry, whose investments have stimulated the enzyme
However, even supporting the biofuels and bioenergy sector, market.
Europe still does not take such an inclusive approach to this The generation of energy from biomass is one of the main
sector (Toivanen and Novotny 2017; Hassan et al. 2019) focus areas of renewable energy programs in India due to
which reflects on the expression of the number of industrial the relatively uniform availability of biomass compared
patents associated with biofuels, firstly China followed by with other renewable sources. This is due to the country’s
the US and Brazil. It clearly reinforces the trends associated agricultural strength, which occupies prominent positions in
with the potential and high investments from these coun- terms of agricultural production, whose main contribution of
tries in technologies for the generation of renewable fuels lignocellulosic residues is from the cultivation of rice, sugar
(Balat and Balat 2009; Rainer et al. 2013; De Figueiredo cane, wheat and cotton (Hiloidhari et al. 2014).
et al. 2018). The provision and use of lignocellulosic biomass to
The first generation of biofuels provide an assurance obtain cellulases have become a promising market in
and using the traditional routes of conversion refers to developing countries, and this alternative is already seen

13

946 Archives of Microbiology (2020) 202:935–951

as an opportunity, which is demonstrated by the number used in this industry is considered mature and consolidated
of documents found that are attributed to India. Likewise, (Sousa and Macedo 2010; Bastos 2012; Machado 2013).
China, which is an agricultural nation, is also prominent The competitive advantages attributed to Brazil with
in the microbial production of cellulases. respect to territorial availability and consolidated technology
China is considered a prolific generator of biomass applied to ethanol may not guarantee the long-term supply
residues, such as straw and forest residues. The main of biofuels (Guevara et al. 2017). For continued progress
use of straw (mainly from rice, wheat and corn crops) in the biofuel industry, Brazil requires great efforts from
is for the conversion into energy through direct combus- the government, industry and universities through scientific
tion and biochemical and physicochemical conversions, research and technical development.
which consolidates the technologies in the country (Irena
2014). The correlated evolution of the microbial cellulase
and bioethanol markets ensures economic benefits to the Distribution of publications by area
country. The technologies involved in the consolidation of of knowledge and origin
the bioprocesses to produce bioethanol have made signifi-
cant progress with respect to research and development in The production and the efficiency of cellulase and hemicel-
recent decades, and it is not the only biochemical product lulase on an industrial scale are important to bioprocessing,
of residual biomass (Fang et al. 2010). which includes the selection and knowledge of the physiol-
Considering its complexities, particularities and chal- ogy of cellulase-producing microorganisms in combination
lenges, the diversification of agricultural activities in with genetic engineering and fermentation process condi-
countries and regions indicates that there is a need for tions. Recent advances in recombinant DNA technology
regional technological solutions (Ferreira-Leitão et al. allow the rapid identification of genes of new cellulase pro-
2010). There is a great diversity of biomass residues in ducers that may enable large-scale production as well as cus-
Brazil that are derived from the agriculture industry, and tom solutions for various industrial applications (Behera and
its bioprocessing could provide significant economic, Ray 2016; Srivastava et al. 2018). Together with bioprocess
social and environmental benefits. Examples of biomass technologies that can guarantee production efficiency, this
residues that are found in Brazil include waste from pulp reflects the distribution of documents included in the respec-
paper, sawdust, sugar cane bagasse, cereal and corn straw, tive areas of study (Fig. 9).
rice husks, smoke powder, etc. (El-Haggar 2007; Castro The search term "environmental sciences" provides repre-
and Pereira Jr 2010). sentativeness in terms of article publication, which is justi-
Brazil is considered a pioneer in the development of tech- fied by the multidisciplinary nature of the field that combines
nologies for the production of biofuels, and even though different sciences such as physics, chemistry and biology
there are less investments compared to the United States to solve environmental problems associated with biomass
and countries in Europe, Brazil is distinguished by reduc- residues. In sequence, areas of study, which include micro-
ing production costs, since it has an economically competi- biology, agricultural and biological sciences and chemical
tive biomass industry based on sugar cane. The technology engineering, appeared in the search results. Publications in

Fig. 9  Distribution of docu-
ments by area of study that
were included in the second
bibliometric analysis using the
terms "cellulase production"
and "microorganism" (Research
2), in the period from 2007 and
2018

13
Archives of Microbiology (2020) 202:935–951 947

these areas of study describe the production of microbial lignocellulosic biomass in the production of microbial cellu-
cellulases involving the selection of microorganisms capable lases; although, the graph created by the VosViewer software
of enhancing biodegradation processes and formulations of for the second bibliometric analysis did not directly refer to
new bioproducts of interest, such as enzymes, in addition residual biomass. The scientific articles that were evaluated
to the development and improvement of thermochemical in this study were published in this journal between 2011
processes that can be used for the pretreatment of residual and 2013. Cellulases are protagonists of the fuel industry
biomass. if residual biomass becomes the raw material that is used
Despite the significant impact and importance of energy to produce bioethanol, which is already a trend that was
issues on the recovery and utilization of biomass waste, sci- initially observed in the bibliometric analysis.
entometric analysis of publications associated with search
terms shows that the subarea of energy is approximately 7%
of the direct references to the terms used in the search. Trends and research opportunities
When verifying the percentage significance of each of the
areas, the final sum exceeded 100%. This is due to the inclu- Many lignocellulosic residues are upcycled and are cur-
sion of more than one area of study in the same publication. rently not properly used with respect to their potential.
In this analysis, some publications were included in four These residues, through the obtained bioproducts, have an
different areas of study, specifically in those areas of study environmental and economic valuation, which allows a new
in which the percentage values were evaluated. approach that is sustainable for agroindustrial processes and
Regarding the origin of the documents that were ana- waste generation. This trend has been observed by Bilal and
lyzed, in the period of time from 2007 to 2018, the jour- colleagues (Bilal et al. 2018) due to the renewable charac-
nal Bioresource Technology published approximately 9% teristic of biofuels.
of all articles, followed by Biotechnology for Biofuels and An incessant search for clean energy is certainly an
Bioresources with 7 and 5%, respectively. Even with a simi- opportunity for reducing costs, using organic waste and
lar number of publications, when the number of citations improving the quality of the environment. Therefore, CBP
received by the respective journals were compared, the per- emerges as an opportunity. The identification and use of
centages reflect differences with respect to the importance native microbial strains that present high cellulolytic and
of microbial cellulase production. Analyzing the number alcoholic activities, fermentation in cocultivation mode
of citations received by scientific papers published in these using different ethanogenic microorganisms with high cel-
journals, approximately 60% of citations are from articles lulolytic potential or the use genetic engineering as a tool to
published in Bioresource Technology, followed by Biotech- obtain recombinant strains of microorganisms that exhibit
nology for Biofuels and Bioresources, with 19 and 15%, high production of cellulases and hemicellulases are strate-
respectively. gies for accomplishing this current approach (Hasunuma and
This higher number of citations from articles published in Kondo 2012; Jouzani and Taherzadeh 2015).
Bioresource Technology specifically corresponds an article It is fundamental that the enzymatic properties of micro-
that received 70% of all citations, "Strain improvement of bial cellulolytic complexes are well studied to improve the
Penicillium janthinellum NCIM 1171 for increased cellulase efficiency of the processes, going beyond factors such as
production” , which was published in 2007 and written by thermal stability and pH of the enzymes that are used. Rec-
Adsul and collaborators. In addition, half of the documents ognizing new microbial strains that express high rates of
included and linked to this journal were published after 2016 enzymatic activity and that have potential uses in biotech-
and may still receive citations in future publications. nological processes for the generation of biofuels and other
Furthermore, articles from the journal Biotechnology materials is fundamentally necessary for the viability and
for Biofuels are more recent, which accounts for the small- technical and economic benefits of bioprocesses.
est number of citations. These articles began receiving Introducing these microorganisms into biotechnological
increased publicity in 2014, which coincides with the grow- processes, especially in the form of microbial cocultures,
ing number of biofuel investments by developing countries, which could take advantage of the specific metabolism of
and the origin of the research published in this journal is each microorganism, may increase the conversion of bio-
mostly articles submitted Chinese researchers. The area of mass into valuable bioproducts and may make these pro-
biofuels is expanding; therefore, jobs that involve the use of cesses viable. The production of large amounts of butyric
microbial cellulases in bioprocesses for the production of acid has been accomplished by cocultivation using a strain of
bioethanol are increasing. Similarly, the citations of research the genus Bacillus and Clostridium tyrotyricum by sucrose
articles in this area of study are also increasing. fermentation (Dwidar et al. 2013). Cocultivation between
The number of citations corresponding to the jour- strains of Clostridium celerecrescens and Clostridium ace-
nal Bioresource Technology indicates the importance of tobutylicum has been studied by Wang et al. (2015) under

13

948 Archives of Microbiology (2020) 202:935–951

mesophilic conditions for the direct conversion of cellulose obtaining bioproducts by enzymatic hydrolysis evolve and
into butanol. In that study, considerable levels of butanol that improvements in the design of bioreactors for the viable
were obtained, demonstrating that the use of consolidated scale up of these processes for commercial and industrial
bioprocesses to obtain biofuels is promising. applications be made.
Enzymes produced by microorganisms can aid in the del-
ignification step of agroindustrial residue and is considered a Acknowledgements  This study was financed in part by the Coorde-
nação de Aperfeiçoamento de Pessoal de Nível Superior—Brasil
sustainable route for the pretreatment of biomass. Therefore, (CAPES)—Finance Code 001. We would like to thank the Ministry
the viability and use of cellulosic ethanol depend on the effi- of Science Technology Innovation and Comunication (MCTIC—
ciency and enzymatic activity, which is related to the final 01.0144.00/2010), the Science and Technology Regional Park (CEP-
value of the product (Rajak and Banerjee 2016). POB-TecnoUnisc) and Science, Technology and Economic Develop-
ment Secretary (SDECT- RS).
For first-generation ethanol, enzymatic technology has
little influence on the final price; for example, for cellulosic
ethanol, it is estimated that 15% of the total cost of pro-
duction is linked to this technology (Ramos et al. 2016).
References
There are few studies related to the use of biocatalysts for Ahmed IN, Yang X-L, Dubale AA, Li R-F, Ma Y-M, Wang L-M, Hou
the pretreatment of biomass and its subsequent production G-H, Guan R-F, Xie M-H (2018) Hydrolysis of cellulose using
of biofuels, which is an area of study with great scientific cellulase physically immobilized on highly stable zirconium
potential (Bilal et al. 2018). based metal-organic frameworks. Bioresour Technol 270:377–
382. https​://doi.org/10.1016/j.biort​ech.2018.09.077
The need to explore, understand and monitor the variables Akram F, Haq IU, Imran W, Mukhtar W (2018) Insight perspectives
that affect the bioprocesses when scaling up the processes of thermostable endoglucanases for bioethanol production: a
are also critical to enable the validation of the industrial review. Renew Energy 122:225–238. https​://doi.org/10.1016/j.
scale fermentation process. These challenges require further renen​e.2018.01.095
Archambault E, Campbell D, Gingras Y, Larivière V (2009) Compar-
study and present opportunities for the design of bioreac- ing bibliometric statistics obtained from the Web of Science and
tors for the profitable commercialization of bioconversion Scopus. J Assoc Inf Sci Technol 60(7):1320–1326. https​://doi.
of agroindustrial waste into bioproducts (Behera and Ray org/10.1002/asi.21062​
2016). Asgher M, Asad MJ, Rahman SU, Legge RL (2007) A thermosta-
ble α-amylase from a moderately thermophilic Bacillus subtilis
Bioconversion of residual biomass in bioproducts is also strain for starch processing. J Food Eng 79(3):950–955. https​://
highlighted as a process aligned with Industry 4.0, which doi.org/10.1016/j.jfood​eng.2005.12.053
provides the integration of vertical and horizontal product Bajpai P (2014a) Sources, production, and classification of xylanases.
manufacturing processes to achieve high levels of indus- In: Bajpai P (ed) Xylanolytic enzymes. Academic Press, Amster-
dam, pp 43–52
trial performance (Dalenogare et al. 2018). Industry 4.0 has Bajpai P (2014b) Sources, production, and classification of xylanases.
been considered one of the main trends in production sys- In: Bajpai P (ed) Xylanolytic enzymes. Academic Press, Amster-
tems, with clear implications for sustainability in organiza- dam, pp 69–104
tions (De Sousa Jabbour et al. 2018; Song and Wang 2016). Balat M, Balat H (2009) Recent trends in global production and utiliza-
tion of bio-ethanol fuel. Appl Energy 86(11):2273–2282. https:​ //
Therefore, technologies 4.0 will enable the automation of doi.org/10.1016/j.apene​rgy.2009.03.015
the various bioprocesses linked to the production of bio- Banerjee A, Chakraborty T, Matsagar V (2018) Evaluation of possi-
products, at the same time that will make them efficient, bilities in geothermal energy extraction from oceanic crust using
planned and optimized, contributing positively to sustain- offshore wind turbine monopiles. Renew Sustain Energy Rev
92:685–700. https​://doi.org/10.1016/j.rser.2018.04.114
able development. Bastos VD (2012) Biorrefinarias, biocombustíveis e química reno-
vável: revolução tecnológica e financiamento. Rev BNDES Rio
de Janeiro 38:85–138
Considerations Behera SS, Ray RC (2016) Solid state fermentation for production
of microbial cellulases: Recent advances and improvement
strategies. Int J Biological Macromol 86:656–669. https​://doi.
A bibliometric and scientometric analyses were conducted org/10.1016/j.ijbio​mac.2015.10.090
that considered the use of agroindustrial waste in the bio- Bilal M, Iqbal HMN, Hu H, Wang W, Zhang X (2018) Metabolic
processing industry and confirmed a trend towards biofuels engineering and enzyme-mediated processing: A biotechno-
logical venture towards biofuel production—a review. Renew
by enzymatic conversion processes. The development of any Sustain Energy Rev 82:436–447. https​: //doi.org/10.1016/j.
bioproduct effectively depends on the efficiency of the bio- rser.2017.09.070
mass preparation and pretreatment stages, yield associated Castro AM, Pereira N Jr (2010) Produção, propriedades e aplicação de
with the high bioconversion rates and purification of the celulases na hidrólise de resíduos agroindustriais. Quím Nova
33(1):181–188. https​: //doi.org/10.1590/S0100​- 40422​0 1000​
bioproduct for subsequent industrial use. 01000​31
There is potential for lignocellulosic residues to be used Chang F, Xue S, Xie X, Fang W, Fang Z, Xiao Y (2018) Carbohy-
in microbial cultures, but it is essential that the processes for drate-binding module assisted purification and immobilization

13
Archives of Microbiology (2020) 202:935–951 949

of β-glucosidase onto cellulose and application in hydrolysis Feres PFD (2010) Os biocombustíveis na matriz energética alemã: pos-
of soybean isoflavone glycosides. J Biosci Bioeng 125(2):185– sibilidades de cooperação com o Brasil. Fundação Alexandre de
191. https​://doi.org/10.1016/j.jbios​c.2017.09.001 Gusmão, Brasília
Collins T, Gerday C, Feller G (2005) Xylanases, xylanase families Ferreira-Leitão V, Gottschalk LM, Ferrara MA, Nepomuceno AL,
and extremophilic xylanases. FEMS Microbiol Rev 29(1):3– Molinari HB, Bom EPS (2010) Biomass residues in Brazil: avail-
23. https​://doi.org/10.1016/j.femsr​e.2004.06.005 ability and potential uses. Waste Biomass Valoriz 1(1):65–76.
Couto SR, Sanromán MA (2006) Application of solid-state fermen- https​://doi.org/10.1007/s1264​9-010-9008-8
tation to food industry—a review. J Food Eng 76(3):291–302. Gomes DG, Serna-Loaiza S, Cardona CA, Gama M, Domingues L
https​://doi.org/10.1016/j.jfood​eng.2005.05.022 (2018) Insights into the economic viability of cellulases recy-
Cunha FM, Badino AC, Farinas CS (2017) Effect of a novel method cling on bioethanol production from recycled paper sludge.
for in-house cellulase production on 2G ethanol yields. Bio- Bioresour Technol 267:347–355. https​://doi.org/10.1016/j.biort​
catal Agric Biotechnol 9:224–229. https​://doi.org/10.1016/j. ech.2018.07.056
bcab.2017.01.007 Gonçalves AR, Benar P, Costa SM, Ruzene DS, Moriya RY, Luz
Silva JA, Pires Bianchi MDL (2001) Cientometria: a métrica da SM, Ferretti LP (2005) Integrated processes for use of pulps
ciência. Paidéia 11(21):5–10. https​://doi.org/10.1590/S0103​ and lignins obtained from sugarcane bagasse and straw. Appl
-863X2​00100​02000​02 Biochem Biotechnol 123(1):821–826. https​://doi.org/10.1385/
Dalenogare LS, Benitez GB, Ayala NF, Frank AG (2018) The ABAB:123:1-3:0821
expected contribution of Industry 4.0 technologies for indus- Gonçalves GA, Takasugi Y, Jia L, Mori Y, Noda S, Tanaka T, Ich-
trial performance. Int J Prod Econ 204:383–394. https​://doi. inose H, Kamiya N (2015) Synergistic effect and application of
org/10.1016/j.ijpe.2018.08.019 xylanases as accessory enzymes to enhance the hydrolysis of
De Figueiredo R, Soletti JI, da Silva SD, Silva JS, Silva K, Esco- pretreated bagasse. Enzyme Microb Technol 72:16–24. https​://
dro PB, Silva DM, Farias KF, Balliano TL (2018) Mapea- doi.org/10.1016/j.enzmi​ctec.2015.01.007
mento Prospectivo das Tecnologias envolvidas na produção Guevara AJ, Silva OR, Hasegawa HL, Venanzi D (2017) Evaluation of
de bioetanol. Cad Prospecção 11(1):127–136. https​: //doi. sustainability of Brazilian ethanol production: a model in system
org/10.9771/cp.v11i1​.23202​ dynamics. Braz Bus Rev 14(4):435–447
De Sousa Jabbour ABL, Jabbour CJC, Foropon C, Godinho Filho M Halevi G, Moed H, Bar-Ilan J (2017) Suitability of Google Scholar
(2018) When titans meet—can industry 4.0 revolutionise the as a source of scientific information and as a source of data for
environmentally-sustainable manufacturing wave? The role of scientific evaluation—review of the Literature. J Informetric
critical success factors. Technol Forecast Soc Change 132:18– 11(3):823–834. https​://doi.org/10.1016/j.joi.2017.06.005
25. https​://doi.org/10.1016/j.techf​ore.2018.01.017 Hassan SS, Williams GA, Jaiswal AK (2019) Moving towards the sec-
Dhabhai R, Chaurasia SP, Dalai AK (2013) Effect of pretreatment ond generation of lignocellulosic biorefineries in the EU: driv-
conditions on strutural characteristics of wheat straw. Chem ers, challenges, and opportunities. Renew Sustain Energy Rev
Eng Commun 200:1251–1259. https​://doi.org/10.1080/00986​ 101:590–599. https​://doi.org/10.1016/j.rser.2018.11.041
445.2012.74389​ Hasunuma T, Kondo A (2012) Development of yeast cell factories
Dwidar M, Kim S, Jeon BS, Um Y, Mitchell RJ, Sang B (2013) for consolidated bioprocessing of lignocellulose to bioethanol
Co-culturing a novel Bacillus strain with Clostridium through cell surface engineering. Biotechnol Adv 30(6):1207–
tyrobutyricum ATCC 25755 to produce butyric acid 1218. https​://doi.org/10.1016/j.biote​chadv​.2011.10.011
from sucrose. Biotechnol Biofuels 6(1):6–35. https​: //doi. Hiloidhari M, Das D, Baruah DC (2014) Bioenergy potential from crop
org/10.1186/1754-6834-6-35 residue biomass in India. Renew Sustain Energy Rev 32:504–
Eisentraut A (2010) Sustainable production of second-generation 512. https​://doi.org/10.1016/j.rser.2014.01.025
biofuels. Potential and perspectives in major economies and Iqbal M, Azam M, Naeem M, Khwaja AS, Anpalagan A (2014) Opti-
developing countries. https​://www.osti.gov/etdew​eb/servl​ets/ mization classification, algorithms and tools for renewable
purl/21330​793. Accessed 10 June 2018 energy: a review. Renew Sustain Energy Rev 39:640–654. https​
El-Haggar SM (2007) Sustainable industrial design and waste man- ://doi.org/10.1016/j.rser.2014.07.120
agement. Academic, Oxford, pp 223–260 Iranmahboob J, Nadim F, Monemi S (2002) Optimizing acid-
Elsevier (2017). Scopus: content coverage guide. Elsevier BV, hydrolysis: a critical step for production of ethanol from mixed
Amsterdam. https​: //www.elsev​i er.com/__data/asset​s /pdf_ wood chips. Biomass Bioenergy 22(5):401–404. https​://doi.
file/0007/69451​/0597-Scopu​s-Conte​nt-Cover​age-Guide​-US- org/10.1016/S0961​-9534(02)00016​-8
LETTE​R-v4-HI-singl​es-no-ticks​.pdf. Accessed 02 July 2018 Irena (2014) Renewable energy prospects: China, REmap 2030 analy-
Ergun SO, Urek RO (2017) Production of ligninolytic enzymes by sis. IRENA, Abu Dhabi. https​://www.irena​.org/remap​. Accessed
solid state fermentation using Pleurotus ostreatus. Ann Agrar 10 June 2018
Sci 15(2):273–277. https​://doi.org/10.1016/j.aasci​.2017.04.003 Jain L, Agrawal D (2018) Performance evaluation of fungal cellu-
Falagas ME, Pitsouni E, Pappas G (2008) Comparison of Pub- lases with dilute acid pretreated sugarcane bagasse: a robust
Med, Scopus, web of science, and Google scholar: strengths bioprospecting strategy for biofuel enzymes. Renew Energy
and weaknesses. The FASEB J. 22(2):338–342. https​: //doi. 115:978–988. https​://doi.org/10.1016/j.renen​e.2017.09.021
org/10.1096/fj.07-9492L​SF Jouzani GS, Taherzadeh MJ (2015) Advances in consolidated bio-
Fang X, Shen Y, Zhao J, Bao X, Qu Y (2010) Status and prospect processing systems for bioethanol and butanol production from
of lignocellulosic bioethanol production in China. Bioresour biomass: a comprehensive review. Biofuel Res J 2(1):152–195
Technol 101(13):4814–4819. https​://doi.org/10.1016/j.biort​ Jung YR, Park JM, Heo S, Hong W, Lee S, Oh B, Park S, Seo J, Kim
ech.2009.11.050 C (2015) Cellulolytic enzymes produced by a newly isolated
Feng CY, Zou SL, Liu C, Zhang K, Hong JF (2016) Zhang MH soil fungus Penicillium sp. TG2 with potential for use in cel-
(2016) Ethanol production from acid- and alkali-pretreated lulosic ethanol production. Renew Energy 76:66–71. https​://doi.
corncob by endoglucanase and β-glucosidase co-expressing org/10.1016/j.renen​e.2014.10.064
Saccharomyces cerevisiae subject to the expression of heter- Jurutu V, Wu JC (2014) Microbial cellulases: engineering, production
ologous genes and nutrition added. World J Microbiol Bio- and applications. Renew Sustain Energy Rev 33:188–203. https​
technol 32:86 ://doi.org/10.1016/j.rser.2014.01.077

13

950 Archives of Microbiology (2020) 202:935–951

Kirk TK, Farrell RL (1987) Enzymatic "combustion": the microbial Paulova L, Patakova P, Branska B, Rychtera M, Melzoch K (2015)
degradation of lignin. Annu Rev Microbiol 41(1):465–501. https​ Lignocellulosic ethanol: technology design and its impact on
://doi.org/10.1146/annur​ev.mi.41.10018​7.00234​1 process efficiency. Biotechnol Adv 33(6):1091–1107. https:​ //doi.
Kogo T, Yoshida Y, Koganei K, Matsumoto H, Watanabe T, Ogihara J, org/10.1016/j.biote​chadv​.2014.12.002
Kasumi T (2017) Production of rice straw hydrolysis enzymes by Pelizer LH, Pontieri MH, Moraes IO (2007) Utilização de resíduos
the fungi Trichoderma reesei and Humicola insolens using rice agro-industriais em processos biotecnológicos como perspec-
straw as a carbon source. Bioresour Technol 233:67–73. https​:// tiva de redução do impacto ambiental. J Technol Manag Innov
doi.org/10.1016/j.biort​ech.2017.01.075 2(1):118–127
Kumar P, Barrett DM, Delwiche MJ, Stroeve P (2009) Methods for Petzold-Welcke K, Daus S, Heinze T (2014) Xylan derivatives and their
pretreatment of lignocellulosic biomass for efficient hydrolysis application potential—mini-review of own results. Carbohydr
and biofuel production. Ind Eng Chem Res 48(8):3713–3729. Polym 100:80–88. https:​ //doi.org/10.1016/j.carbpo​ l.2012.11.052
https​://doi.org/10.1021/ie801​542g Polizeli M, Rizzatti AC, Monti R, Terenzi HF, Jorge JA, Amorim DS
Ladeira SA, Cruz E, Delatorre AB, Barbosa JB, Martins MLL (2015) (2005) Xylanases from fungi: properties and industrial appli-
Cellulase production by thermophilic Bacillus sp SMIA-2 and cations. Appl Microbiol Biotechnol 67(5):577–591. https​://doi.
its detergent compatibility. Electron J Biotechnol 18(2):110–115 org/10.1007/s0025​3-005-1904-7
Lopes S, Costa MT, Fernández-Llimós F, Amante MJ, Lopes PF (2012) Rainer J, Turhollow AF, Rutz D, Mergner R (2013) Production facili-
A Bibliometria e a Avaliação da Produção Científica: indicadores ties for second-generation biofuels in the USA and the EU—cur-
e ferramentas. Actas do congresso Nacional de bibliotecários, rent status and future perspectives. Biofuels Bioprod Biorefin
arquivistas e documentalistas, n1. https:​ //www.bad.pt/public​ acoe​ 7(6):647–665. https​://doi.org/10.1002/bbb.1451
s/index​.php/congr​essos​bad/artic​le/view/429. Accessed 15 Nov. Rajak R, Banerjee R (2016) Enzyme mediated biomass pretreatment
2018 and hydrolysis: a biotechnological venture towards bioetha-
Lopes ML, Paulillo SCDL, Godoy A, Cherubin RA, Lorenzi MS, nol production. RSC Adv 6(66):61301–61311. https​: //doi.
Giometti FHC, Bernardino CD, Amorim Neto HB, Amorim org/10.1039/C6RA0​9541K​
HV (2016) Ethanol production in Brazil: a bridge between Ramos JL, Valdivia M, García-Lorente F, Segura A (2016) Benefits and
science and industry. Braz J Microbiol 47:64–76. https​://doi. perspectives on the use of biofuels. Microb Biotechnol 9(4):436–
org/10.1016/j.bjm.2016.10.003 440. https​://doi.org/10.1111/1751-7915.12356​
Lynd LR, Weimer PJ, van Zyl WH, Pretorius IS (2002) Microbial Reese ET (1956) Enzymatic hydrolysis of cellulose. Appl Microbiol
cellulose utilization: fundamentals and biotechnology. Micro- 4(1):39–45
biol Mol Biol Rev 66(3):506–577. https​://doi.org/10.1128/ Reetz MT (2010) Enzyme engineering by directed evolution. In: Baltz
mmbr.66.3.506-577.2002 RH, Demain AL, Davies JE, Junker B, Katz L, Lynd L, Mas-
Machado CMM (2013) Microrganismos na produção de biocombus- urekar P, Reeves C, Zhao H (eds) Manual of industrial microbiol-
tíveis líquidos. Embrapa Agroenergia, Brasília ogy and biotechnology, 3rd edn. American Society for Microbi-
Malherbe S, Cloete TE (2002) Lignocellulose biodegradation: fun- ology Press, Washington, pp 466–479
damentals and applications. Rev Environ Sci Biotechnol Rodrigues C, Woiciechowski AL, Letti LA Jr, Karp SG, Goelzer FD,
1(2):105–114 Sobral KCA, Coral JD, Campioni TS, Maceno MAC, Soccol
McMillan JD (1994) Pretreatment of lignocellulosic biomass. In: Him- CR (2017) Materiais lignocelulósicos como matéria prima para
mel ME, Baker JO, Overend RP (eds) Enzymatic conversion of a obtenção de biomoléculas de valor comercial. In: Resende RR
biomass for fuels production. ACS Publications, Washington, (ed) Biotecnologia Aplicada a Agro&indústria, vol 4. Blucher,
pp 292–324 São Paulo, pp 283–314
Mood SH, Golfeshan AH, Tabatabaei M, Jouzani GS, Najafi GH, Ruiz-Dueñas FJ, Martínez AT (2009) Microbial degradation of lignin:
Gholami M, Ardjmand M (2013) Lignocellulosic biomass to how a bulky recalcitrant polymer is efficiently recycled in nature
bioethanol, a comprehensive review with a focus on pretreatment. and how we can take advantage of this. Microb Biotechnol
Renew Sustain Energy Rev 27:77–93. https​://doi.org/10.1016/j. 2(2):164–177. https:​ //doi.org/10.1111/j.1751-7915.2008.00078.​ x
rser.2013.06.033 Sadhu S, Maiti TK (2013) Cellulase production by bacteria: a review.
Moraïs S, Heyman A, Barak Y, Caspi J, Wilson DB, Lamed R, Sho- Br Microbiol Res J 3(3):235–258
seyov O, Bayer EA (2010) Enhanced cellulose degradation by Santos RNMD, Kobashi NY (2009) Bibliometria, cientometria, info-
nano-complexed enzymes: synergism between a scaffold-linked metria: conceitos e aplicações. Pesq Bras Ci Inf 2(1):155–172
exoglucanase and a free endoglucanase. J Biotechnol 147(3– Screena CP, Sebastian D (2018) Augmented cellulase production by
4):205–211. https​://doi.org/10.1016/j.jbiot​ec.2010.04.012 Bacillus subtilis strain MU S1 using different statistical experi-
Motta FL, Andrade CCP, Santana MHA (2013) A review of xylanase mental designs. J Genet Eng Biotechnol 16(1):9–16. https​://doi.
production by the fermentation of xylan: classification, char- org/10.1016/j.jgeb.2017.12.005
acterization and applications. In: Chandel A, Silva SS (eds) Shajahan S, Moorthy G, Sivakumar N, Selvakumar G (2017) Statistical
Sustainable degradation of lignocellulosic biomass techniques, modeling and optimization of cellulase production by Bacillus
applications and commercialization. Intech, Rijeka, pp 251–275 licheniformis NCIM 5556 isolated from the hot spring, Maha-
Naidu DS, Hlangothi SP, John MJ (2018) Bio-based products from rashtra. India. J King Saud Univ Sci 29(3):302–310. https​://doi.
xylan: a review. Carbohydr Polym 179:28–41. https​: //doi. org/10.1016/j.jksus​.2016.08.001
org/10.1016/j.carbp​ol.2017.09.064 Shallom D, Shoham Y (2003) Microbial hemicellulases. Curr
Nguyen Q, Bowyer J, Howe J, Bratkovich S, Groot H, Pepke E, Fern- Opin Microbiol 6(3):219–228. https​://doi.org/10.1016/s1369​
holz K (2017) Global production of second generation biofuels: -5274(03)00056​-0
trends and influences. Dovetail Partners Inc, Minneapolis, pp Sharma S, Yazdani SS (2016) Diversity of microbial cellulase system.
1–16 In: Gupta VK (ed) New and future developments in microbial
Nyko D, Garcia JLF, Milanez AY, Dunham FB (2010) A corrida tec- biotechnology and bioengineering Microbial cellulase system
nológica pelos biocombustíveis de segunda geração: uma per- properties and applications. Elsevier, Amsterdam, pp 49–64
spectiva comparada. BNDES Setorial, Rio de Janeiro, pp 5–48 Singhania RR, Adsul M, Pandey A, Patel AK (2017) Cellulases. In:
Patra SK, Bhattacharya P, Verma N (2006) Bibliometric study of litera- Pandey A, Negi S, Socco C (eds) Current developments in
ture on bibliometrics. DESIDOC J Libr Inf Technol 26(1):27–32 biotechnology and bioengineering Production, isolation and

13
Archives of Microbiology (2020) 202:935–951 951

purification of industrial products. Elsevier, Amsterdam, pp Paredes JR (2019) Contribution of variable renewable energy
73–101 to increase energy security in Latin America: complementarity
Song C, Qiu Y, Liu Q, Ji N, Zhao Y, Kitamura Y, Hou X (2018) Pro- and climate change impacts on wind and solar resources. Renew
cess intensification of cellulosic ethanol production by waste Sustain Energy Rev 113:109232. https​: //doi.org/10.1016/j.
heat integration. Chem Eng Res Des 132:115–122. https​://doi. rser.2019.06.039
org/10.1016/j.cherd​.2018.01.016 Vohra M, Manwar J, Manmode R, Padgilwar S, Patil S (2014) Bioetha-
Song M, Wang S (2016) Can employment structure promote environ- nol production: Feedstock and current technologies. J Environ
ment-biased technical progress? Technol Forecast Soc Change Chem Eng 2:573–584. https:​ //doi.org/10.1016/j.jece.2013.10.013
112:285–292. https​://doi.org/10.1016/j.techf​ore.2016.02.016 Wang Z, Cao G, Zheng J, Fu D, Song J, Zhang J, Zhao L, Yang Q
Souza MR (2012) Microbial degradation of lignocellulosic biomass. In: (2015) Developing a mesophilic co-culture for direct conversion
Chandel A, Silva SS (eds) Sustainable degradation of lignocel- of cellulose to butanol in consolidated bioprocess. Biotechnol
lulosic biomass techniques, applications and commercialization. Biofuels 8(1):1–9. https​://doi.org/10.1186/s1306​8-015-0266-3
Intech, Rijeka, pp 207–247 White W, Mandels G, Siu R (1950) Fungi in relation to the degra-
Souza De (2013) Microbial degradation of lignocellulosic biomass. In: dation of woolen fabrics. Mycol 42(2):199–223. https​://doi.
Chandel AK, Silva SS (eds) Sustainable degradation of lignocel- org/10.2307/37554​33
lulosic biomass—techniques, applications and commercializa- Yang SQ, Yan QJ, Jiang ZQ, Li LT, Tian HM, Wang YZ (2006) High-
tion. InTech, Rijeka, pp 207–247 level of xylanase production by the thermophilic Paecilomyces
Sóti V, Lenaerts S, Cornet I (2018) Of enzyme use in cost-effective themophila J18 on wheat straw in solid-state fermentation. Biore-
high solid simultaneous saccharification and fermentation pro- sour Technol 97(15):1794–1800. https​://doi.org/10.1016/j.biort​
cesses. J Biotechnol 270:70–76. https​://doi.org/10.1016/j.jbiot​ ech.2005.09.007
ec.2018.01.020 Ye Y, Li X, Cao Y, Du J, Chen S, Zhao J (2017) A β-xylosidase hyper-
Sousa ED, Macedo IDC (2010) Etanol e bioeletricidade: a cana-de- production Penicillium oxalicum mutant enhanced ethanol pro-
açúcar no futuro da matriz energética. Luc Projetos de Comuni- duction from alkali-pretreated corn stover. Bioresour Technol
cação, São Paulo 245:734–742. https​://doi.org/10.1016/j.biort​ech.2017.08.155
Srivastava N, Srivastava M, Mishra PK, Gupta K, Molina G, Rodri- Yu H, Li X (2015) Alkali-stable cellulase from a halophilic isolate,
guez-Couto S, Manikanta A, Ramteke PW (2018) Applications Gracilibacillus sp. SK1 and its application in lignocellulosic sac-
of fungal cellulases in biofuel production: advances and limi- charification for ethanol production. Biomass Bioenery 81:19–
tations. Renew Sustain Energy Rev 82:2379–2386. https​://doi. 25. https​://doi.org/10.1016/j.biomb​ioe.2015.05.020
org/10.1016/j.rser.2017.08.074 Yuan B, Yang XQ, Xue LW, Feng YN, Jiang JH (2016) A novel recy-
Sun Y, Cheng J (2002) Hydrolysis of lignocellulosic materials for etha- cling system for nano-magnetic molecular imprinting immobi-
nol production: a review. Bioresour Technol 83(1):1–11. https​:// lised cellulases: synergistic recovery of anthocyanin from fruit
doi.org/10.1016/S0960​-8524(01)00212​-7 and vegetable waste. Bioresour Technol 222:14–23. https​://doi.
Thomas L, Parameswaran B, Pandey A (2016) Hydrolysis of pretreated org/10.1016/j.biort​ech.2016.09.088
rice straw by an enzyme cocktail comprising acidic xylanase Zhang PHY, Himmel ME, Mielenz JR (2006) Outlook for cellulase
from Aspergillus sp. for bioethanol production. Renew Energy improvement: screening and selection strategies. Biotechnol Adv
98:9–15. https​://doi.org/10.1016/j.renen​e.2016.05.011 24(5):452–481. https:​ //doi.org/10.1016/j.biotec​ hadv.​ 2006.03.003
Thomas L, Ram H, Singh VP (2018) Inducible cellulase production Zhang X, Li Y, Zhao X, Bai F (2017) Constitutive cellulase produc-
from an organic solvent tolerant Bacillus sp SV1 and evolu- tion from glucose using the recombinant Trichoderma ree-
tionary divergence of endoglucanase in different species of the sei strain overexpressing an artificial transcription activator.
genus Bacillus. Braz J Microbiol 49(2):429–442. https​://doi. Bioresour Technol 223:317–322. https​://doi.org/10.1016/j.biort​
org/10.1016/j.bjm.2017.05.010 ech.2016.10.083
Toivanen H, Novotny M (2017) The emergence of patent races in lig- Zhang YHP, Lynd LR (2004) Toward an aggregated understanding of
nocellulosic biofuels, 2002–2015. Renew Sustain Energy Rev enzymatic hydrolysis of cellulose: noncomplexed cellulase sys-
77:318–326. https​://doi.org/10.1016/j.rser.2017.03.089 tems. Biotechnol Bioeng 88(7):797–824. https:​ //doi.org/10.1002/
UNEP (2018) UN Environment’s Economy Division. Global Trands in bit.20282​
Renewable Energy Investiment
Valencia EY, Chambergo FS (2013) Mini-review: Brazilian fungi Publisher’s Note Springer Nature remains neutral with regard to
diversity for biomass degradation. Fungal Genet Biol 60:9–18. jurisdictional claims in published maps and institutional affiliations.
https​://doi.org/10.1016/j.fgb.2013.07.005
Viviescas C, Lima L, Diuana FA, Vasquez E, Ludovique C, Silva
GN, Huback V, Magalar L, Szklo A, Lucena FP, Schaeffer R,

13

You might also like