Literature DB >> 31647988

Review: The structure and function of cellulase (endo-β-1,4-glucanase) and hemicellulase (β-1,3-glucanase and endo-β-1,4-mannase) enzymes in invertebrates that consume materials ranging from microbes, algae to leaf litter.

Stuart M Linton1.   

Abstract

This review discusses the reaction catalysed, and the structure and function of the cellulase, endo-β-1,4-glucanase and the hemicellulase enzymes, β-1,3-glucanase and endo-β-1,4-mannase that are present in numerous invertebrate groups with a diverse range of feeding specialisations. These range from microbial deposit and filter feeders, micro and macrophagous algal feeders, omnivores to herbivorous leaf litter and wood feeders. Endo-β-1,4-glucanase from glycosyl hydrolase family 9 (GH9) digests cellulose like β-1,4-glucans from a range of materials. As it hydrolyses crystalline cellulose very slowly, it is a poor cellulase. Where tested, the enzyme has dual endo-β-1,4-glucanase and lichenase activity. Its presence does not necessarily indicate the ability of an animal to digest cellulose. It only indicates the ability to digest β-1,4-glucans and its function, which is discussed in this review, should be considered with reference to the substrates present in the diet. β-1,3-glucanase (laminarinase) belongs to glycosyl hydrolase family 16 (GH16) and hydrolyses β-1.3-glucans. These polysaccharides are present in the cell walls of algae, protozoans and yeast, and they also occur as storage polysaccharides within protozoans and algae. Depending on their site of expression, these enzymes may function as a digestive enzyme or may be involved in innate immunity. Enzymes present in the digestive fluids or tissues, would be digestive. Haemolymph GH16 proteins may be involved in innate immunity through the activation of the phenol oxidase system. Insect GH16 proteins expressed within the haemolymph have lost their catalytic residues and function as β-glucan binding proteins. In contrast, crustacean GH16 proteins expressed within the same tissue, have retained the catalytic residues and thus possibly their β-1,3-glucanase activity. The potential function of which is discussed. Endo-β-1,4-mannase from glycosyl hydrolase family 5, subfamily 10 (GH5_10) hydrolyses mannan, glucomannan and galactomannan. These hemicelluloses are present in the cell walls of plants and algae and also function as storage polysaccharides within legume and palm seeds. They are digestive enzymes whose high expression in some species suggests they are a major contributor to hemicellulose digestion. They may also provide the animal with substantial amounts of monosaccharides for energy. Crown
Copyright © 2019. Published by Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 31647988     DOI: 10.1016/j.cbpb.2019.110354

Source DB:  PubMed          Journal:  Comp Biochem Physiol B Biochem Mol Biol        ISSN: 1096-4959            Impact factor:   2.231


  7 in total

1.  Evolution of a major virion protein of the giant pandoraviruses from an inactivated bacterial glycoside hydrolase.

Authors:  Mart Krupovic; Natalya Yutin; Eugene Koonin
Journal:  Virus Evol       Date:  2020-11-30

2.  Characterization and Functional Importance of Two Glycoside Hydrolase Family 16 Genes from the Rice White Tip Nematode Aphelenchoides besseyi.

Authors:  Hui Feng; Dongmei Zhou; Paul Daly; Xiaoyu Wang; Lihui Wei
Journal:  Animals (Basel)       Date:  2021-02-02       Impact factor: 2.752

Review 3.  Role of metagenomics in prospecting novel endoglucanases, accentuating functional metagenomics approach in second-generation biofuel production: a review.

Authors:  Ninian Prem Prashanth Pabbathi; Aditya Velidandi; Tanvi Tavarna; Shreyash Gupta; Ram Sarvesh Raj; Pradeep Kumar Gandam; Rama Raju Baadhe
Journal:  Biomass Convers Biorefin       Date:  2021-01-07       Impact factor: 4.987

4.  The characteristics of insoluble softwood substrates affect fungal morphology, secretome composition, and hydrolytic efficiency of enzymes produced by Trichoderma reesei.

Authors:  Vera Novy; Fredrik Nielsen; Daniel Cullen; Grzegorz Sabat; Carl J Houtman; Christopher G Hunt
Journal:  Biotechnol Biofuels       Date:  2021-04-26       Impact factor: 6.040

Review 5.  Bioethanol Production by Enzymatic Hydrolysis from Different Lignocellulosic Sources.

Authors:  Katja Vasić; Željko Knez; Maja Leitgeb
Journal:  Molecules       Date:  2021-02-01       Impact factor: 4.411

6.  Significant differences in intestinal fungal community of hooded cranes along the wintering periods.

Authors:  Yuannuo Wu; Zihan Li; Jingru Zhao; Zhong Chen; Xingjia Xiang
Journal:  Front Microbiol       Date:  2022-09-07       Impact factor: 6.064

7.  Cellobiose phosphorylase from Caldicellulosiruptor bescii catalyzes reversible phosphorolysis via different kinetic mechanisms.

Authors:  Shaowei Bai; Liangzhen Yang; Honglei Wang; Chao Yang; Xuechen Hou; Jingjie Gao; Zuoming Zhang
Journal:  Sci Rep       Date:  2022-03-10       Impact factor: 4.996

  7 in total

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