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Edited by
Ashok Pandey, Sangeeta Negi,
Carlos Ricardo Soccol
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xxi
xxii List of Contributors
A.K. Patel DBT-IOC Centre for Advanced Bioenergy Research, IndianOil Corporation
Limited
xxiv List of Contributors
Ashok Pandey
Professor Ashok Pandey is Eminent Scientist at the Center of
Innovative and Applied Bioprocessing, Mohali (a national
institute under the Department of Biotechnology, Ministry
of Science and Technology, Government of India), and
former chief scientist and head of the Biotechnology
Division at the CSIR’s National Institute for Interdisciplinary
Science and Technology at Trivandrum. He is an adjunct
professor at Mar Athanasios College for Advanced Studies
Thiruvalla, Kerala, and at Kalasalingam University, Krishnan
Koil, Tamil Nadu. His major research interests are in the
areas of microbial, enzyme, and bioprocess technology,
which span various programs, including biomass to fuels
and chemicals, probiotics and nutraceuticals, industrial
enzymes, solid-state fermentation, etc. He has more than
1100 publications and communications, which include 16
patents, 50+ books, 125 book chapters, and 425 original and review papers, with an h index
of 75 and more than 23,500 citations (Google Scholar). He has transferred several tech-
nologies to industries and has been an industrial consultant for about a dozen projects for
Indian and international industries.
Professor Pandey is the recipient of many national and international awards
and fellowships, which include Elected Member of the European Academy of Sciences
and Arts, Germany; Fellow of the International Society for Energy, Environment and
Sustainability; Fellow of the National Academy of Science (India); Fellow of the Biotech
Research Society, India; Fellow of the International Organization of Biotechnology and
Bioengineering; Fellow of the Association of Microbiologists of India; honorary doctorate
degree from the Université Blaise Pascal, France; Thomson Scientific India Citation
Laureate Award, United States; Lupin Visiting Fellowship; Visiting Professor at the
Université Blaise Pascal, France, the Federal University of Parana, Brazil, and the École
Polytechnique Fédérale de Lausanne, Switzerland; Best Scientific Work Achievement
Award, Government of Cuba; UNESCO Professor; Raman Research Fellowship Award,
CSIR; GBF, Germany, and CNRS, France fellowships; Young Scientist Award; and others.
He was chairman of the International Society of Food, Agriculture and Environment,
Finland (Food & Health) during 2003e04. He is the Founder President of the Biotech
xxvii
xxviii About the Editors
Sangeeta Negi
Dr. Sangeeta Negi is an assistant professor in the Department
of Biotechnology at the Motilal Nehru National Institute of
Technology, India. She has a First Class Master’s degree in
biochemistry and a PhD in biotechnology from the Indian
Institute of Technology, Kharagpur. She has also worked as
an academic guest at the Biological Engineering Department,
Polytech Clermont-Ferrand; the Université Blaise Pascal,
France; and the Bioenergy and Energy Planning Research
Group, Swiss Federal Institute of Technology, Lausanne,
Switzerland. Dr. Negi’s current research interests are in the
areas of biofuels, industrial enzymes, and bioremediation. She is an editorial board
member of the Journal of Waste Conversion, Bioproducts and Biotechnology and the Journal
of Environmental Science and Sustainability. She has been awarded as Outstanding
Reviewer by Elsevier and has won the Young Scientist Award by DST at the National
Seminar on Biological and Alternative Energies Present and Future, organized by Andhra
University, Visakhapatnam, in 2009. She has also won the Best Poster Award at the
International Congress on Bioprocesses in Food Industries (2008) at Hyderabad. Dr. Negi
has contributed to nearly 70 publications, including review articles, original papers, and
conference communications.
About the Editors xxix
This book is a part of the comprehensive series Current Developments in Biotechnology and
Bioengineering, comprising nine volumes (Editor-in-chief: Ashok Pandey), and deals with the
production, isolation, and purification of industrial products produced by biotechnological
processes. This book covers recent technological advances of a great number of biotechno-
logical products and is divided into four different parts: Production of Industrial and
Therapeutic Enzymes, Organic Acids, Biopolymers and Other Products, and Products
Isolation and Purification.
Part 1 is devoted to the production of industrial and therapeutic enzymes. The first
chapter describes the current and future trends of production, application, and strain
improvement of a-amylases, one of the most important enzymes used in industry.
a-Amylases find application in several industrial processes, such as starch liquefaction,
desizing of textiles, detergents, baking, bioethanol production, etc. Glucoamylase is another
enzyme extensively used in the food and fermentation industries, mainly for the saccharifi-
cation of starch, brewing, and production of high-fructose syrup, which are discussed in
Chapter 2. Cellulases, b-glucosidases, and xylanases are the second most used enzymes in
industry by sales volume, with an increasing demand since 1995 in several industrial appli-
cations, comprising detergents and textiles, animal feed, food, paper, and biofuels. These
enzymes are discussed in Chapters 4, 5, and 6 of this book. Chapter 7 discusses proteolytic
enzymes, also known as “proteases,” which are used to cleave the peptide bonds connecting
two amino acids. They are produced mainly by microorganisms and have great commercial
value, being used in food, dairy, detergents, and leather processing. Lipolytic enzymes are
hydrolases comprising 15 families of lipases, as shown in Chapter 8 of this book through a
study of the industrial applications and other important aspects of these enzymes. The
purpose of Chapters 9 and 10 is to present an overview of laccases and peroxidases, covering
their production and use in the pretreatment of lignocellulosic biomass and biopulping, and
also projecting new perspectives on improving such processes and products using these
enzymes. Sources of production, strategies, characteristics, applications, and industrial
importance of therapeutic enzymes, such as L-glutaminase, L-asparaginase, and penicillin
acylase, are presented and discussed in Chapters 11, 12, and 13. Other enzymes, such as
phytases, chitinases, keratinases, tannases, aminopeptidases, nattokinases, and poly-
saccharide lyases, are reviewed in Chapters 14 to 23, covering recent advances, production
methods, potential applications, and the global market.
The second part of the book is dedicated to organic acids. In Chapters 24 and 25, lactic
acid and citric acid production, synthesis (covering factors that affect biochemical pathways),
and recovery are addressed. Chapter 26 reviews the microbial production of gluconic acid,
properties of glucose oxidase, production, recovery, and applications. Succinic acid is an
important platform molecule, used as an intermediate in the production of numerous
everyday products, among which are pharmaceuticals and adhesives, representing a total
immediate addressable market of more than $7.2 billion. Chapter 27 presents an analysis of
the current market, biological-based production processes, enzymatic regulation, and
recovery systems of succinic acid.
xxxi
xxxii Preface
Part 3 discusses polymer production and other products. Polylactide (PLA), derived
from lactic acid, a biodegradable polyester, has applications in packaging, textiles, and the
biomedical and pharmaceutical industries. Chapter 28 reviews the properties and applica-
tions of PLA, focusing on recent technologies and improvement of production techniques.
Polyhydroxyalkanoates (PHAs), a family of environmentally friendly polyesters that can be
synthesized by a wide range of microorganisms as carbon and energy reserves, have been
considered an alternative to petroleum-based chemicals. The composition and structural
diversity of PHAs have led to various properties and endless applications to form a PHA value
chain. Chapter 29 briefly introduces their production and application, highlighting the lab-
oratory production by the microbial strains developed using genetic and/or metabolic en-
gineering or synthetic biology techniques. Industrial production, recent technologies, and
improvement of PHA production are also discussed. Poly-g-glutamic acid (g-PGA) is a natural
polymer, synthesized by various strains of Bacillus spp., that is used in food, cosmetics,
agriculture, and the wastewater industry. Chapter 30 provides updated information on the
biosynthesis, fermentation, purification, and application of g-PGA. In Chapter 31, recent
developments in the biological production of 1,3-propanediol by various natural and
genetically engineered microorganisms, nonnative 1,3-propanediol producers, as well as
mixed cultures, are discussed. Important aspects of downstream processing and various
methods and steps involved in the extraction and purification of 1,3-propanediol from the
fermentation broth are also covered in this chapter. The production of petroleum-based
plastics is a challenging environmental problem, causing the production and consumption
of biodegradable plastics to receive considerable attention nowadays. Chapter 32 provides an
overview of the degradation mechanisms of biodegradable polymers, with particular
emphasis on the main parameters affecting the degradation of these polymeric biomaterials.
In Chapter 33 the potential of biological control is presented and discussed as a promising
alternative to chemical pesticides. The final two chapters of this book, Chapters 34 and 35,
present the most relevant downstream processes to extract, isolate, purify, and refine
fermentation products.
We are confident that this book will be profitable to students, professors, researchers,
and professionals interested in studying biotechnology and bioengineering. We thank
Dr. Kostas Marinakis, Book Acquisition Editor; Ms. Anneka Hess; and entire production team
at Elsevier for their help and support in bringing out this volume.
Editors
Ashok Pandey
Sangeeta Negi
Carlos Ricardo Soccol
1
a-Amylases
1.1 Introduction
1.1.1 Starch
Starch is the major polysaccharide food reserve in nature after cellulose. It serves as an
important source of nutrition for other living organisms [1]. It is synthesized in the
plastids present in leaves and accumulates as insoluble granules in higher and lower
plants. Starch is composed of a large number of glucose units joined by glycosidic bonds.
It consists of two types of molecules: amylose and amylopectin. Amylose is a linear,
water-insoluble polymer of glucose joined by a-1,4 bonds, whereas amylopectin is a
branched, water-soluble polysaccharide with short a-1,4-linked linear chains of 10e60
glucose units and a-1,6-linked side chains with 15e45 glucose units. The levels of
amylase and amylopectin vary among different starches. Generally, starch is composed
of amylose and amylopectin in the range 25e28% and 72e75%, respectively.
1.1.2 Amylases
Amylases are the enzymes that break down starch, or glycogen. These enzymes are
produced by a variety of living organisms, ranging from bacteria to plants to humans.
Though amylases are produced by several microorganisms, those produced by fungi and
bacteria have dominated applications in the industrial sector [2]. Bacteria and fungi
secrete amylases to the outside of their cells to carry out extracellular digestion, which
breaks down the insoluble starch, and then the soluble end products (such as glucose or
maltose) are absorbed into the cells.
Amylases constitute a class of industrial enzymes occupying about 25% of the enzyme
market. Because of the increasing demand for these enzymes in various industries, there
is enormous interest in developing them with better properties, such as raw starch-
degrading amylases suitable for industrial applications, and cost-effective production
*
Corresponding Author.
Current Developments in Biotechnology and Bioengineering: Production, Isolation and Purification of Industrial Products
http://dx.doi.org/10.1016/B978-0-444-63662-1.00001-4 3
Copyright © 2017 Elsevier B.V. All rights reserved.
4 CURRENT DEVELOPMENTS IN BIOTECHNOLOGY AND BIOENGINEERING
techniques. Although amylases can be derived from several sources, including plants,
animals, and microorganisms, microbial enzymes generally meet industrial demands.
A large number of microbial amylases are available commercially and they have almost
completely replaced the chemical hydrolysis of starch in the starch processing industry
[3]. One of the most important advantages of using microbes for the production of
amylases is the bulk production capacity and the fact that microbes can be genetically
modified to produce enzymes with desired characteristics [4]. These enzymes are of great
significance in biotechnology, with various applications ranging from food, fermentation,
and textiles to the paper industry. Each application of a-amylase requires unique
properties with respect to specificity, stability, and temperature and pH dependence.
Modern technologies such as computational packages and online servers are the
current tools used in protein sequence analysis and characterization. The physico-
chemical and structural properties of these proteins are well understood with the use of
computational tools. The protein sequence profile, such as number of amino acids and
sequence length, and the physicochemical properties of the protein, such as molecular
weight, atomic composition, extinction coefficient, aliphatic index, instability index, etc.,
can be computed by ProtParam, and the secondary structure prediction, sequence
similarity, evolutionary relationships, and 3-D structure of various proteins can be
computed using the ESyPred3D server [5].
products. Exoamylases are enzymes that cleave a-1,4, or a-1,6 bonds of the external
glucose residues resulting in a- or b-anomeric products. Debranching enzymes are
enzymes that hydrolyze a-1,6 bonds leaving linear polysaccharides. Transferases are
enzymes that cleave a-1,4 glycosidic bonds of the donor molecule and transfer part of
the donor molecule to a glycosidic acceptor, forming a new glycosidic bond [7].
respectively. The enzyme produced high levels of maltose from potato starch, suggesting
its usefulness in the commercial production of maltose and glucose syrups. The study
conducted by Krishna and Chandrasekharan [28] revealed that banana peel could be
utilized as a potential substrate for a-amylase production by A. niger. Saxena and Singh
[29] screened various agro-industrial residues for amylase production from Bacillus sp.
and found mustard oil cake to be the best substrate. The strain produced 5400 U/g of
amylase at 1:3 moisture content, 20% inoculum, and an incubation period of 72 h. Yang
and Wang [30] reported a-amylase production by Streptomyces rimosus TM 55 using
sweet potato residue and peanut meal residue as a substrate. The strain produced
1903 U of a-amylase after 96 h of incubation.
Ramachandran et al. [20] used coconut oil cake (COC), a by-product of oil extraction
from dried copra, as a substrate for the production of a-amylase from fungi. COC sup-
plemented with 0.5% starch and 1% peptone enhanced a-amylase production by
A. oryzae. COC serves as a source of soluble proteins and lipids thus providing essential
nutrients for the growth of and enzyme synthesis by the organism. Production of
a-amylase by B. amyloliquefaciens under SSF using corn gluten meal (CGM) was re-
ported by Saban et al. [31]. The study revealed that a-amylase production in a medium
with CGM was five times higher than that in a medium containing starch and other
components. Utilization of CGM as a substrate makes the process economically viable
because CGM is a by-product of starch-based industries.
Production and optimization of a-amylase from A. oryzae CBS 819 using a by-product
of wheat grinding (gruel) as the sole carbon source was done by Kammoun et al. [32].
Various process parameters affecting the production were optimized by adopting a
BoxeBehnken design, which increased the enzyme production from 40.1 to 151.1 U/mL.
Murthy et al. [33] reported coffee by-products as suitable substrate for the production of
a-amylase under SSF. Coffee waste was converted into value-added products by
fermentation using Neurospora crassa CFR 308. The optimum conditions for a-amylase
production were moisture content of 60%, pH 4.5, incubation temperature of 27 C,
particle size of 1 mm, and incubation time of 5 days. Under optimized conditions the
strain produced 7084 U/gds of a-amylase.
Syed et al. [34] reported extracellular amylase production by Streptomyces gulbar-
gensis DAS 131 by SmF. The highest amylase production was observed when the medium
was supplemented with 1% starch. The enzyme was thermotolerant and stable at pH 9.0.
Starch and peptone were good sources of carbon and nitrogen. Sharma and
Satyanarayana [13] reported enhanced production of acidic high-maltose-forming and
Ca2þ-independent a-amylase by B. acidicola; a maximum enzyme titer of 366 IU/L was
attained after 36 h of fermentation at pH 4.5, 33 C, with 0.5 vvm aeration. The enzyme
titer was 10,100 IU/L in fed-batch fermentation. One of the main advantages of fed-
batch fermentation over the batch fermentation is that the concentration of limiting
substrate is maintained at low levels, thus avoiding the repressing effect of high substrate
concentration and thereby minimizing the accumulation of inhibitory metabolites.
Another random document with
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The Project Gutenberg eBook of Mr. Belloc
still objects to Mr. Wells's "Outline of history"
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Language: English
BY
HILAIRE BELLOC
E * S * A
PUBLISHERS AND IMPORTERS
* * * * *
Mr. Wells’s pamphlet against me, to which I am here replying, is a
web of six elements. These are not put in any regular order, and the
author himself would probably not be capable of analysing them; but a
competent critic has no difficulty in separating them one from the other.
They are:—
First: A number of shrill grievances on general grounds. For
instance, that though I have praised him highly I have not praised him
highly enough; that where I had to blame him I have used adjectives
upon his work such as “confused,” “ignorant,” which were not
warranted; that in general he is an ill-used fellow, and is moved to
complain most bitterly.
Secondly: He violently (and this is the main gist of all his pamphlet)
assaults me for pointing out that his statement of Darwinian Natural
Selection as the chief agent of evolution is antiquated stuff, exploded,
and proves him quite unacquainted with modern work. Here he jeers at
me as putting on a pose of special learning, and challenges me to
quote any modern authorities substantiating my criticism. He calls my
argument fantastic, a thing made up out of my own head, without any
authority from competent biologists. He denies the existence of any
such group of modern men of science opposed to Darwinian Natural
Selection. It is an amazing thing that his ignorance should reach such
a level as that, but it does. And it is there I am going to hammer him.
Thirdly: There runs all through the little pamphlet, and still more
through the book itself, a startling ignorance upon the Catholic Church,
and in particular the idea that the Church is opposed to scientific work,
even such elementary science as Mr. Wells attempts to expound.
Fourthly: He complains that I have in certain specific points
misread his meaning, misstated his conclusions or affirmations, and
made errors myself in attempting to correct his. He brings, it is true, no
more than three specific allegations; three out of a total of I know not
how many score, in a body of work which catches him up and exposes
him over and over again. Nevertheless, such as they are, being
specific allegations, however few, they must in justice be met; and I will
here meet them.
Fifthly: (and most significant): There is the embarrassed silence of
Mr. Wells’s pamphlet: his inability to meet nine-tenths of the points I
have brought against him, and his discreet shirking all mention of
them.
Sixthly: The book ends with Mr. Wells’s usual glorious vision of a
glorious Millennium contrasted with the sad blindness of Catholics in
general, and myself in particular, to this approaching Seventh
Monarchy.
I will deal with these six matters which build up Mr. Wells’s
pamphlet, taking them in the order I have given.
I
MR. WELLS’S GENERAL GRIEVANCES