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International Journal of Biological Macromolecules 66 (2014) 74–80

Contents lists available at ScienceDirect

International Journal of Biological Macromolecules


journal homepage: www.elsevier.com/locate/ijbiomac

Review

Locust bean gum: Processing, properties and food


applications—A review
Sheweta Barak, Deepak Mudgil ∗
Department of Dairy and Food Technology, Mansinhbhai Institute of Dairy and Food Technology, Mehsana 384002, Gujarat, India

a r t i c l e i n f o a b s t r a c t

Article history: Locust bean gum or carob gum is a galactomannan obtained from seed endosperm of carob tree i.e.
Received 28 December 2013 Ceratonia siliqua. It is widely utilized as an additive in various industries such as food, pharmaceuticals,
Received in revised form 4 February 2014 paper, textile, oil well drilling and cosmetics. Industrial applications of locust bean gum are due to its
Accepted 9 February 2014
ability to form hydrogen bonding with water molecule. It is also beneficial in the control of many health
Available online 16 February 2014
problems like diabetes, bowel movements, heart disease and colon cancer due to its dietary fiber action.
This article focuses on production, processing, composition, properties, food applications and health
Keywords:
benefits of locust bean gum.
Locust bean gum
Carob bean gum © 2014 Elsevier B.V. All rights reserved.
Dietary fiber
Properties
Food application

Contents

1. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
2. Production . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
3. Processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
4. Non-food applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
5. Composition and chemical structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
6. Properties . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
6.1. Solubility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
6.2. Rheology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
6.3. Viscosity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
6.4. Hydration rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
6.5. Synergistic gel formation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
6.6. Water adsorption isotherm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7. Food applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7.1. Edible films/coating . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7.2. Beverages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7.3. Bakery products . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7.4. Noodles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7.5. Ice cream . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
7.6. Low-fat yoghurt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
8. Health benefits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
9. Conclusions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79

∗ Corresponding author. Tel.: +91 9896672001.


E-mail address: dsmudgil@yahoo.com (D. Mudgil).

http://dx.doi.org/10.1016/j.ijbiomac.2014.02.017
0141-8130/© 2014 Elsevier B.V. All rights reserved.
Author's personal copy

S. Barak, D. Mudgil / International Journal of Biological Macromolecules 66 (2014) 74–80 75

1. Introduction other hydrocolloid such as ␬-carrageenan; it improves the prop-


erties of the film due to its synergistic action. LBG is also used
Locust bean gum is a white to creamy white powder obtained as thickener, stabilizer and gelling agent in various food products
after milling of seed endosperm of fruit pod of the carob tree, a such as baked foods, beverages, dairy products and processed fruit
member of legume family, botanically known as Ceratonia siliqua L. products. Locust bean gum is classified as GRAS (Generally recog-
which is found in Mediterranean regions. Hence, locust bean gum nized as safe) by FDA and is used for its stabilizing, thickening and
is also known as carob gum. The carob seed is consists of three parts fat-replacing properties [13].
i.e. husk, endosperm and germ. The processing of carob gum first
involves the removal of hull from the seed which can be attained
2. Production
via thermo-mechanical or by chemical treatment [1]. After removal
of the outer layer i.e. the hull, the seeds are split lengthwise and
Locust bean gum is extracted from the seed endosperm of the
the germ portion is separated from the endosperm of carob seed.
carob tree plant botanically known as C. siliqua. It belongs to the
Further, the isolated endosperms are subjected to grinding, sift-
subfamily Caesalpinioideae of the Leguminosae family [14]. Carob
ing, grading, packaging and finally marketed as locust bean gum or
plant is typical tree of semiarid environments. It is very abundant in
LBG. All the operations in LBG processing are designed such that
the Mediterranean region since ancient times and is currently pro-
any impurity from husk or germ portion can be avoided which can
duced in Spain, Italy, Cyprus and other Mediterranean countries.
ultimately alter the properties of the carob gum. Galactomannans
Its localization also extends to different regions of North Africa,
are linear polysaccharides consists of ␤-(l–4)-mannose backbone
South America, and Asia. Other known carob producing countries
with single d-galactopyranosyl units attached via ␣-(l–6) linkages
are Morocco, Greece, Algeria, Turkey, Israel, India and Pakistan.
as side branch. These side branches are not distributed uniformly in
Carob plant is long-lived evergreen tree and after germination, it
the main backbone chain [2,3]. There are also present some unsub-
grows to about 10 m height in 10–15 years. The carob tree may not
stituted ␤-d-mannopyranosyl chain segments, alternating with
be fully grown until it is 50 years old and it starts to bear good
␤-d-mannopyranosyl units substituted with ␣-d-galactopyranosyl
quantities of pods at the age of 15 years. The pods reach to full size
side branches [4–7]. Carob galactomannan is one of the commercial
in July but are ripened in October. Hot and dry climatic conditions
galactomannans guar gum and tara gum; and among these galac-
are required for good yields. Large trees can yield up to half ton
tomannans LBG has the lowest galactose content about twenty
of pods per annum. Carob tree yields large brown fruits known as
percent [8]. Locust bean gum generally has an average mannose
carob pods. These carob pods are sickle shaped and are 10–20 cm
to galactose ratio of about 3.5 which is highest among the com-
in length and 2–4 cm in width. These sickle shaped pods contain
mercially available galactomannan such as guar gum (1.8) and
10–15 oval shaped carob seeds or kernels. The polysaccharide from
tara gum (3.0). The degree of galactose substitution on mannose
seed endosperm of carob tree is also referred in the literature as
chain affects water solubility of the galactomannan. This is reason
carob bean gum, carob seed gum, carob flour, or even ceratonia
because guar gum is cold water soluble whereas LBG shows low sol-
[15]. World production of carob seeds is estimated at about 315,000
ubility at ambient temperature and there is a requirement of heat
tons per year, produced from two lakhs hectare. The main produc-
treatment for maximum solubility to achieve the best water bind-
ers include Morocco (38%), Spain (28%), Italy (8%), Portugal (8%),
ing capacity [9]. The molecular size, mannose to galactose ratio,
Greece (6%), Turkey (6%) and Cyprus (2%) [14]. Recently, growing
galactose distribution in the mannose backbone chain influences
interest for locust bean gum has been observed due to its various
solubility and also controls the rheological properties of LBG. Differ-
industrial applications. Locust bean gum is used as a thickening and
ent chromatography techniques can be used to characterize carob
stabilizing agent in food, cosmetic and pharmaceuticals industries
galactomannan structure. The molecular weight distributions can
[16]. In food industry it is a food additive with E-number E-410
be determined using size exclusion chromatography and mannose
in the European Union [17]. Pharmaceutical applications of locust
to galactose ratio can be generally determined using gas chro-
bean gum are mainly due to its ability as controlled release excipi-
matography. LBG is considered as the first galactomannan used as
ent in tablets. Biodegradability, low toxicity and low cost of locust
additive in industries such as paper industry, textile industry, phar-
bean gum contribute for its increasing utilization in various fields.
maceutical industry, cosmetic industry and food industries. The
important characteristic of this gum that make it a useful indus-
trial gum is its ability to form very viscous aqueous solution at 3. Processing
relatively low concentration, to stabilize emulsion and to replace
fat in many food products. Being non-ionic in nature, locust bean The carob pods are kibbled to separate the seeds from the pulp
gum solutions are not influenced by pH, salts and heat treatment. portion. The processing of carob seeds includes dehusking (acid
Locust bean gum can be used in combination with other hydrocol- or thermo-mechanical), splitting, milling, sifting, clarification and
loids such as carrageenan and xanthan gum as it shows synergistic drying. The processing of carob seeds is very difficult due to its
action with them and forms a gel with more elasticity and strength very tough and hard seed coat. The dehusking of carob kernels is
[10]. Locust bean gum is suitable for many food applications as it achieved by treatment of carob seeds with dilute sulphuric acid
provides a creamy mouthfeel. It is typically added in cream-cheese or with thermo-mechanical treatment known as acid peeling and
spreads to impart richness and spreadability. It is especially useful thermal peeling, respectively. In acid peeling process, carob seeds
in preventing syneresis in various food products. LBG also create a are treated with sulphuric acid at elevated temperature to car-
smooth mouthfeel in sauces. LBG’s ability to bind water makes it bonize the seed coat. The remaining portions of the seed coat are
an excellent choice for frozen applications, such as ice cream as it separated and removed from the endosperm portion by efficient
will slow down and reduces the size of ice-crystal formation as the washing and brushing process. The peeled kernels are dried and
moisture is retained within the ice cream. LBG also finds applica- cracked and the more friable germ gets crushed. The germ parts
tion in yoghurt manufacture. In yoghurt, it reduces the syneresis are sifted off from the unbroken endosperm halves known as splits.
and enhances water holding capacity of yoghurt when used at cer- The carob bean gum produced from the carob splits by this process
tain levels [11]. Recently, LBG is used in edible films and improved is whitish in color and has higher viscosity. In thermo-mechanical
the properties of films such as water vapor permeability, oxygen peeling process, roasting of carob kernels are carried out in rotating
permeability, tensile strength and elongation-at-break [12]. In edi- furnace where the seed coat gets pop off from the internal portions
ble coatings, when locust bean gum is used in combination with of carob kernels. The endosperm halves or carob splits are obtained
Author's personal copy

76 S. Barak, D. Mudgil / International Journal of Biological Macromolecules 66 (2014) 74–80

Table 1
Composition of carob seed.

Part Proportion (%)

Husk 30–33
Endosperm 42–46
Germ 23–25

Locust bean gum also reduces or controls diabetes due to its high
gelling ability which on ingestion causes satiety sensation [20].
In textile industry, locust bean gum is used in combination with
starch as sizing agent. Locust bean gum is utilized as a thickener in
paints. Locust bean gum is also used in paper making, pet foods and
cosmetics products.

5. Composition and chemical structure

Locust bean kernel is composed three major components which


are outer husk (30–33%), germ portion (23–25%) and endosperm
portion (42–46%) by seed weight (Table 1). The major portion
of locust bean endosperm is galactomannan, which comprises
approximately 80% weight of the endosperm and the rest corre-
sponding to proteins and impurities. The protein content of locust
bean gum is reported to include albumin and globulin (32%), while
the remaining 68% correspond to glutelin [21]. Impurities mainly
refer to ash and acid-insoluble matter [22]. After seed processing,
crude galactomannan can be further submitted to several processes
Fig. 1. Flow diagram for manufacturing of locust bean gum. to eliminate both the protein content and impurities. Impurities
usually remain insoluble even when heating at temperatures up to
after mechanical processing and are recovered from the roasted 70 ◦ C [23]. Treatment with isopropanol is considered very efficient
seed coat or husk and the crashed germs. The isolated endosperm in the elimination of proteins as insoluble impurities. The com-
halves are milled and sieved to obtain fine particle size powder of position of commercial locust bean gum is presented in Table 2.
native carob bean gum or locust bean gum (Fig. 1). The product The commercial locust bean gum powder contains approximately
obtained from this process is somewhat darker in color due to the 10–12% moisture, 5% protein, 1.0% ash, 1.0% crude fiber, 0.5% fat and
heating or roasting operation. Thermo-mechanical process leads to 80–85% galactomannan [24,25]. Possible impurities in commercial
no effluent as it do not involve sulphuric acid as processing aid. Clar- locust bean gum powder are husk and germ which are reflected by
ification of native locust bean gum may be achieved by dispersing it acid-insoluble matter and protein content, respectively. Residual
in water and dissolved by heating. This solution is subjected to fil- amount of ethanol or isopropanol used during washing or extrac-
tration to remove insoluble substances and to obtain clear solution. tion process also act as impurities in locust bean gum powder.
Locust bean gum is recovered by precipitation with isopropanol or Locust bean gum is comprised of a high molecular weight
ethanol, followed by filtering, drying and grinding or milling, to polysaccharide composed of galactomannan. Locust bean galac-
obtain fine particle size powder of clarified or purified carob bean tomannan is composed of two units i.e. galactose and mannose.
gum. Locust galactomannan consists of a linear chain of (1→4)-linked ␤-
d-mannopyranosyl units with (1→6)-linked ␣-d-galactopyranosyl
4. Non-food applications residues as side chains (Fig. 2). Locust galactomannans are highly
polydispersed like other polysaccharides found in nature. In lit-
Locust bean pods were utilized as cattle feed for a very long erature molecular weight of locust galactomannan is reported as
time but now its seed endosperm powder is utilized as locust bean approximately 310,000. However, recent molecular weight estima-
gum in various industries such as food, cosmetic, pharmaceutical, tion techniques such as gel permeation chromatography suggest
textile, paint, mining, oil drilling and construction industries for that average molecular weight of locust galactomannan varies sig-
its thickening and stabilizing properties. In pharmaceutical indus- nificantly, typically ranging from 0.3 to 2.0 million, depending on
tries, locust bean gum is used in the production of solid monolithic the seed source, plant growing conditions and manufacturing pro-
matrix systems, films, beads, micro-particles, nano-particles, inhal- cesses. The galactomannan molecule is considered to exhibit an
able and injectable systems, as well as in viscous liquid and gel extended ribbon-like structure at the solid state and a semi flex-
formulations. In these dosage forms, locust bean gum performs dif- ible coil-like conformation in solution. The galactose to mannose
ferent functions such as binders, viscosity enhancers, stabilizers, ratio of locust bean gum is approximately 1:3.1–1:3.9 [25–27]. The
matrix formers, drug release modifiers, coatings, disintegrators,
solubilizers, emulsifiers, suspending agents, gelling agents, and Table 2
bioadhesives [18]. Biopharmaceutical applications of locust bean Composition of locust bean gum.
gum are mainly attributed to its gelling capacity and synergies with Constituent Proportion (%)
other polysaccharides. The most common application of locust bean
Galactomannan 80.0–85.0
gum is the formulation of oral delivery systems based on tablets, Moisture 10.0–12.0
hydrogels and multiparticulate systems. Apart from the binding Protein content 5.0–6.0
and stabilizing ability, locust bean gum also act as a bioactive Fat content 0.5–0.9
substance which has hypolipidemic effect, decreasing low density Crude fiber 0.8–1.0
Ash 0.5–1.0
lipoprotein (LDL) cholesterol due to high dietary fiber content [19].
Author's personal copy

S. Barak, D. Mudgil / International Journal of Biological Macromolecules 66 (2014) 74–80 77

Fig. 2. Structure of locust bean gum.

mannose and galactose content has been reported as 77–78% and molecules aligns in the direction of flow which leads to decrease
21–23%, respectively [25]. The distribution of d-galactosyl residues in viscosity and thus explain the non-Newtonian behavior of locust
or side chains along the mannose backbone chain can be random, bean gum solution at higher shear rates [29].
blockwise and ordered. Aqueous solutions of locust bean gum at 0.5–2.0% concentra-
tion shows a typical behavior of macromolecular biopolymer with
6. Properties dominating loss modulus (G ) over storage modulus (G ) in lower
frequency range whereas storage modulus dominates the loss
The functional properties of locust galactomannan like other modulus in high frequency range. It means that locust bean gum
polysaccharides are dependent on their behavior in an aque- solutions with concentrations ranging from 0.5% to 2.0%, shows a
ous medium. Locust bean gum is partially soluble in cold water. liquid behavior at lower frequency (G > G ) and a solid-like behav-
Locust galactomannan requires heating for complete solubilization ior at higher frequencies (G > G ). G value of locust bean gum
in water. If galactomannan sol is heated above 80 ◦ C to achieve aqueous solution at same concentration is lower than fenugreek
complete solubilization, care should be taken, as heating to such galactomannan, guar galactomannan and tara galactomannan. In
extent may cause oxidative–reductive depolymerization of galac- frequency sweep tests, crossover frequency (where G = G ) of locust
tomannan chain and reduction in viscosity of final solution may bean gum solution shifts to lower frequency values with increase
observed. In pH range 4–9, The Viscosity of locust bean gum solu- in gum concentration [30].
tion decreases with pH increasing above 9 and decreasing below
4. Locust bean gum is relatively stable against mechanical distor- 6.3. Viscosity
tion. The viscosity property of locust bean gum depends on various
factors such as molecular weight, concentration, shear rate and The most significant property of locust bean gum is its ability
solubilization method. Locust bean gum is often regarded as less to hydrate in hot water to give viscous solution. The thick-
viscous than guar gum and tara gum. ening capacity of locust bean gum depends on certain factors
such as particle size, polymer concentration, molecular weight
6.1. Solubility distribution, shear rate, solubilization methods and impurities.
Locust bean gum is generally less viscous galactomannan than
Locust bean gum is partially soluble in cold water and needs guar and tara galactomannan. Viscosity values of locust bean
to be heated to reach maximum solubility. Locust bean gum gum solutions in the Newtonian plateau can be used to ana-
shows solubility in water of approximately 70–85% when heated lyze molecular characteristics. Intrinsic viscosity of locust bean
to 80 ◦ C/30 min [28]. This difference in solubility may be due to gum solution is determined based on concentration dependence
the high molecular weight galactomannan component and galac- of Newtonian viscosities of dilute solutions. Intrinsic viscosity is
tomannan with lower galactose residues as side chain which can related molecular weight through a power-law equation known
solubilized at higher temperature. It shows that it is hot water sol- as Mark–Houwink–Sakurada equation. Power-law exponent ‘˛’ for
uble and has lesser solubility in water than other galactomannans locust bean gum has been reported as 0.77 when water is used
such as guar gum which is cold water soluble gum [5]. Generally, the as solvent. Intrinsic viscosity and molecular weight of locust bean
solubility of locust bean gum powder does not exceed 90%, which is gum is lower among galactomannans. Viscosity of locust bean gum
further dependent on some factors or variable such as particle size solutions is concentration dependent and generally shows increase
or granulation and impurities such as husk or germ contamination with increase in gum concentration.
[16].
6.4. Hydration rate
6.2. Rheology
Rate of hydration of commercial locust bean gum varies depend-
Rheology is the study of flow (in liquids) and deformation (in ing on the grades. Locust bean gum is generally graded based on the
solid or semisolids) of material under the effect of applied force. particle size, gum content and insoluble. Locust bean gum requires
Locust bean gum in aqueous solutions shows a non-Newtonian heating at 80 ◦ C for 30 min for its full hydration. Hydration of about
behavior (pseudoplastic steady-flow behavior or shear-thinning 2 h is required in order to reach maximum viscosity for practi-
behavior) at high shear rates, but exhibits Newtonian flow behavior cal applications [31]. Major controlling factor of hydration rate of
at low shear rates. At lower shear rates, the disruption of molecular locust bean gum is particle size of locust bean gum powder. Fine
entanglements by the shear may be balanced by the reforma- particle size gum powder hydrates easily and more quickly than
tion of new entanglements, so that the viscosity kept constant relatively coarser particle size gum powder. Commercially, fine par-
and the locust bean gum solutions show Newtonian flow behav- ticle size locust bean gum powder is available for quick hydration.
ior whereas at higher shear rates, disruption of the entanglements However, a considerable time interval for complete or maximum
predominated over the reformation of new entanglements, hydration of locust bean gum powder is still desired.
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78 S. Barak, D. Mudgil / International Journal of Biological Macromolecules 66 (2014) 74–80

6.5. Synergistic gel formation or without the addition of plasticizers and surfactants [12]. Locust
bean gum has been used to form edible films/coatings due to its
Locust bean gum do not form gel under normal conditions but edibility and biodegradability and can be used as an alternative
upon freeze–thaw treatment a weak gel can be obtained. Locust to reduce negative effects of minimal processing on fresh-cut fruits
bean gum forms gel in the presence of large amount of sucrose. [36]. Hydrophilic properties of locust bean gum provide a good bar-
Gel strength of locust bean solution in combination with sugar rier due to its carbon dioxide permeability, oxygen permeability,
shows an initial increase and subsequent decrease with increas- water vapor permeability, tensile strength and elongation-at-break
ing concentration of sugar. Initial increase in gel strength may under certain conditions. Locust bean gum in edible film and
be attributed to reduction in water content due to increased coating may also serve as carrier of additives and bioactive com-
concentration of sugar. The subsequent decrease in gel strength ponents [37]. Edible films formed by mixed systems of locust bean
attributed to inhibition of polymer–polymer association by bind- gum and ␬-carrageenan showed improved properties. The addi-
ing of sugar molecules to polymer chains which leads to decrease tion of ␬-carrageenan to locust bean gum improved the barrier
in gel strength arising from decrease in strength of binding. Maxi- properties of the film which leads to decrease in water vapor per-
mum gel strength of locust bean gum solutions can be attained at meability. Improved values of elongation-at-break of edible films
45% (by weight) fructose, 50% (by weight) sucrose or sorbitol, and were also reported when the ratio of ␬-carrageenan and locust
55% (by weight) glucose [32]. Locust bean gum also shows a useful bean gum was mixed in the ratio of 80:20% (w/w). ␬-carrageenan
synergistic increase in gel strength on blending with other gums and locust bean gum blend films enhance the tensile strength
such as xanthan gum, ␬-carrageenan etc. X-ray diffraction analysis compared to tensile strength of films prepared individually by ␬-
of xanthan-locust bean gum blends shows new diffraction patterns carrageenan and locust bean gum. Improvement in ␬-carrageenan
that are absent in xanthan and locust bean when studied separately and locust bean gum film properties are reported due to hydro-
which suggest intermolecular binding between xanthan and locust gen bonds interactions between ␬-carrageenan and locust bean
bean gum. X-ray diffraction studies also indicate random aggre- gum observed via Fourier Transform Infrared (FTIR) spectroscopy
gation between galactomannan and ␬-carrageenan which reveals analysis [38].
small degree of intermolecular binding. It is well accepted fact
that by replacement part of carrageenan with locust bean gum, 7.2. Beverages
increases the gel strength indexed by dynamic rigidity modulus
and compressive Young’s modulus. This increase in gel strength Locust bean gum is very popular as thickening and stabilizing
increases with increase in concentration of locust bean gum and agent in used in various beverages. Locust bean gum solutions are
then decreases after a peak point in mixed gel and is generally stable at wide range of pH which makes it a unique stabilizer and
known as synergistic effect [33]. thickener in most of the beverages. Guar gum is soluble in hot water
and most of the beverages require heat processing which enable
6.6. Water adsorption isotherm the locust bean gum to use in beverages. It improves the keep-
ing qualities of beverages via resistance to phase separation and
Water adsorption isotherm represents the relationship between thickening.
equilibrium moisture content vs. water activity. Torres et al. (2012)
studied the water adsorption isotherm of locust bean gum at 7.3. Bakery products
different temperatures (20–65 ◦ C) and reported increase in equilib-
rium moisture content with increasing water activity following the Its application for bakery purposes results in higher baked prod-
shape corresponding to type II isotherms according to Brunauer’s uct yields; it improves the final texture and adds viscosity in dough.
classification [34,35]. Torres et al. (2012) also reported that the Addition of guar gum in cookies dough improves the machinabil-
equilibrium moisture content of locust bean gum decreased with ity of the dough which helps in the better handling of dough with
increasing temperature at each water activity level [35]. This can minimum requirement of energy and time. Locust bean gum is also
be explained as at high temperatures, the activation of water used to increase volume and to retard the aging of bakery products
molecules changes to higher energy levels and the links become less [39]. The addition of locust bean gum to wheat flour suspension
stable and break away from the water-binding sites of galactoman- decreases the pasting temperature and increases the peak viscos-
nan, hence the equilibrium moisture content decreases. Isosteric ity, trough viscosity, breakdown, final viscosity and setback values.
sorption heat of locust bean gum decreased with increasing equi- Water absorption capacity and dough development time of wheat
librium moisture content. Locust bean gum shows high sorption flour dough also increases on addition of locust bean gum [40].
heat of about 27 kJ mol−1 which exhibits less hygroscopicity of the Locust bean gum can also be used as binding agent as a substitute
gum [35]. for gluten in gluten-free bread formulations based on corn starch
with improved loaf volume and crumb structure [41].
7. Food applications
7.4. Noodles
Locust bean gum is used as an additive in food industry due to its
thickening and stabilizing property. Its utilization as stabilizer and Incorporation of locust bean gum in noodles dough improves
thickener in food products is popular as it is obtained from a natural the dough rheology as well as the textural characteristics of the
source. Its functionality is due to its water phase management in cooked noodles. Improvement in textural properties of noodles is
food products. attributed to the strengthening effect of gum on the gluten network
which results in better textural properties of noodles. Addition of
7.1. Edible films/coating locust bean gum reduces the cooking loss and swelling index of
noodles [42].
The use of edible films or coatings composed of natural poly-
mers and food additives have been constantly increasing in the 7.5. Ice cream
food industry to enhance the shelf life of fresh fruits, vegetables
and meat products. These films/coatings can be produced from Locust bean gum alone or in combination with guar gum is
biopolymers such as polysaccharides, proteins, lipids, resins, with used in frozen dairy products for desired textural properties such
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S. Barak, D. Mudgil / International Journal of Biological Macromolecules 66 (2014) 74–80 79

as viscosity enhancement and ice recrystallization inhibition. But, it is utilized as thickener and stabilizer in ice cream, sauce, bever-
milk proteins and locust bean gum systems are incompatible in ages, bakery and meat industry. It is also a source of soluble fiber
solution systems and leads to separation of phases [43]. These and can be utilized for the development of dietary fiber enriched
two separated phase consists of water soluble and water insoluble food products. Its consumption in routine diet reduces the risk of
components. Water insoluble components include colloidal protein heart diseases, diabetes and digestive disorders in human beings.
and fat components (opaque); whereas other phase include dis-
solved solutes (transparent). The difference in optical properties
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