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Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria
In bacteria, glycogen plays important roles in carbon and energy storage. Its structure has recently been linked with bacterial environmental durability. Among the essential genes for bacterial glycogen metabolism, the glgB-encoded branching enzyme GBE plays an essential role in forming α-1,6-glycos...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6339891/ https://www.ncbi.nlm.nih.gov/pubmed/30692986 http://dx.doi.org/10.3389/fmicb.2018.03354 |
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author | Wang, Liang Liu, Qinghua Hu, Junfeng Asenso, James Wise, Michael J. Wu, Xiang Ma, Chao Chen, Xiuqing Yang, Jianye Tang, Daoquan |
author_facet | Wang, Liang Liu, Qinghua Hu, Junfeng Asenso, James Wise, Michael J. Wu, Xiang Ma, Chao Chen, Xiuqing Yang, Jianye Tang, Daoquan |
author_sort | Wang, Liang |
collection | PubMed |
description | In bacteria, glycogen plays important roles in carbon and energy storage. Its structure has recently been linked with bacterial environmental durability. Among the essential genes for bacterial glycogen metabolism, the glgB-encoded branching enzyme GBE plays an essential role in forming α-1,6-glycosidic branching points, and determines the unique branching patterns in glycogen. Previously, evolutionary analysis of a small sets of GBEs based on their N-terminal domain organization revealed that two types of GBEs might exist: (1) Type 1 GBE with both N1 and N2 (also known as CBM48) domains and (2) Type 2 GBE with only the N2 domain. In this study, we initially analyzed N-terminal domains of 169 manually reviewed bacterial GBEs based on hidden Markov models. A previously unreported group of GBEs (Type 3) with around 100 amino acids ahead of the N1 domains was identified. Phylogenetic analysis found clustered patterns of GBE types in certain bacterial phyla, with the shorter, Type 2 GBEs predominantly found in Gram-positive species, while the longer Type 1 GBEs are found in Gram-negative species. Several in vitro studies have linked N1 domain with transfer of short oligosaccharide chains during glycogen formation, which could lead to small and compact glycogen structures. Compact glycogen degrades more slowly and, as a result, may serve as a durable energy reserve, contributing to the enhanced environmental persistence for bacteria. We were therefore interested in classifying GBEs based on their N-terminal domain via large-scale sequence analysis. In addition, we set to understand the evolutionary patterns of different GBEs through phylogenetic analysis at species and sequence levels. Three-dimensional modeling of GBE N-termini was also performed for structural comparisons. A further study of 9,387 GBE sequences identified 147 GBEs that might belong to a possibly novel group of Type 3 GBE, most of which fall into the phylum of Actinobacteria. We also attempted to correlate glycogen average chain length (ACL) with GBE types. However, no significant conclusions were drawn due to limited data availability. In sum, our study systematically investigated bacterial GBEs in terms of domain organizations from evolutionary point of view, which provides guidance for further experimental study of GBE N-terminal functions in glycogen structure and bacterial physiology. |
format | Online Article Text |
id | pubmed-6339891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63398912019-01-28 Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria Wang, Liang Liu, Qinghua Hu, Junfeng Asenso, James Wise, Michael J. Wu, Xiang Ma, Chao Chen, Xiuqing Yang, Jianye Tang, Daoquan Front Microbiol Microbiology In bacteria, glycogen plays important roles in carbon and energy storage. Its structure has recently been linked with bacterial environmental durability. Among the essential genes for bacterial glycogen metabolism, the glgB-encoded branching enzyme GBE plays an essential role in forming α-1,6-glycosidic branching points, and determines the unique branching patterns in glycogen. Previously, evolutionary analysis of a small sets of GBEs based on their N-terminal domain organization revealed that two types of GBEs might exist: (1) Type 1 GBE with both N1 and N2 (also known as CBM48) domains and (2) Type 2 GBE with only the N2 domain. In this study, we initially analyzed N-terminal domains of 169 manually reviewed bacterial GBEs based on hidden Markov models. A previously unreported group of GBEs (Type 3) with around 100 amino acids ahead of the N1 domains was identified. Phylogenetic analysis found clustered patterns of GBE types in certain bacterial phyla, with the shorter, Type 2 GBEs predominantly found in Gram-positive species, while the longer Type 1 GBEs are found in Gram-negative species. Several in vitro studies have linked N1 domain with transfer of short oligosaccharide chains during glycogen formation, which could lead to small and compact glycogen structures. Compact glycogen degrades more slowly and, as a result, may serve as a durable energy reserve, contributing to the enhanced environmental persistence for bacteria. We were therefore interested in classifying GBEs based on their N-terminal domain via large-scale sequence analysis. In addition, we set to understand the evolutionary patterns of different GBEs through phylogenetic analysis at species and sequence levels. Three-dimensional modeling of GBE N-termini was also performed for structural comparisons. A further study of 9,387 GBE sequences identified 147 GBEs that might belong to a possibly novel group of Type 3 GBE, most of which fall into the phylum of Actinobacteria. We also attempted to correlate glycogen average chain length (ACL) with GBE types. However, no significant conclusions were drawn due to limited data availability. In sum, our study systematically investigated bacterial GBEs in terms of domain organizations from evolutionary point of view, which provides guidance for further experimental study of GBE N-terminal functions in glycogen structure and bacterial physiology. Frontiers Media S.A. 2019-01-14 /pmc/articles/PMC6339891/ /pubmed/30692986 http://dx.doi.org/10.3389/fmicb.2018.03354 Text en Copyright © 2019 Wang, Liu, Hu, Asenso, Wise, Wu, Ma, Chen, Yang and Tang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Wang, Liang Liu, Qinghua Hu, Junfeng Asenso, James Wise, Michael J. Wu, Xiang Ma, Chao Chen, Xiuqing Yang, Jianye Tang, Daoquan Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria |
title | Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria |
title_full | Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria |
title_fullStr | Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria |
title_full_unstemmed | Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria |
title_short | Structure and Evolution of Glycogen Branching Enzyme N-Termini From Bacteria |
title_sort | structure and evolution of glycogen branching enzyme n-termini from bacteria |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6339891/ https://www.ncbi.nlm.nih.gov/pubmed/30692986 http://dx.doi.org/10.3389/fmicb.2018.03354 |
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