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The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19

The glycoside hydrolase 19 (GH19) is a bifunctional family of chitinases and endolysins, which have been studied for the control of plant fungal pests, the recycle of chitin biomass, and the treatment of multi-drug resistant bacteria. The GH19 domain-containing sequences (22,461) were divided into a...

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Autores principales: Orlando, Marco, Buchholz, Patrick C. F., Lotti, Marina, Pleiss, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547705/
https://www.ncbi.nlm.nih.gov/pubmed/34699529
http://dx.doi.org/10.1371/journal.pone.0256817
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author Orlando, Marco
Buchholz, Patrick C. F.
Lotti, Marina
Pleiss, Jürgen
author_facet Orlando, Marco
Buchholz, Patrick C. F.
Lotti, Marina
Pleiss, Jürgen
author_sort Orlando, Marco
collection PubMed
description The glycoside hydrolase 19 (GH19) is a bifunctional family of chitinases and endolysins, which have been studied for the control of plant fungal pests, the recycle of chitin biomass, and the treatment of multi-drug resistant bacteria. The GH19 domain-containing sequences (22,461) were divided into a chitinase and an endolysin subfamily by analyzing sequence networks, guided by taxonomy and the substrate specificity of characterized enzymes. The chitinase subfamily was split into seventeen groups, thus extending the previous classification. The endolysin subfamily is more diverse and consists of thirty-four groups. Despite their sequence diversity, twenty-six residues are conserved in chitinases and endolysins, which can be distinguished by two specific sequence patterns at six and four positions, respectively. Their location outside the catalytic cleft suggests a possible mechanism for substrate specificity that goes beyond the direct interaction with the substrate. The evolution of the GH19 catalytic domain was investigated by large-scale phylogeny. The inferred evolutionary history and putative horizontal gene transfer events differ from previous works. While no clear patterns were detected in endolysins, chitinases varied in sequence length by up to four loop insertions, causing at least eight distinct presence/absence loop combinations. The annotated GH19 sequences and structures are accessible via the GH19 Engineering Database (GH19ED, https://gh19ed.biocatnet.de). The GH19ED has been developed to support the prediction of substrate specificity and the search for novel GH19 enzymes from neglected taxonomic groups or in regions of the sequence space where few sequences have been described yet.
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spelling pubmed-85477052021-10-27 The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19 Orlando, Marco Buchholz, Patrick C. F. Lotti, Marina Pleiss, Jürgen PLoS One Research Article The glycoside hydrolase 19 (GH19) is a bifunctional family of chitinases and endolysins, which have been studied for the control of plant fungal pests, the recycle of chitin biomass, and the treatment of multi-drug resistant bacteria. The GH19 domain-containing sequences (22,461) were divided into a chitinase and an endolysin subfamily by analyzing sequence networks, guided by taxonomy and the substrate specificity of characterized enzymes. The chitinase subfamily was split into seventeen groups, thus extending the previous classification. The endolysin subfamily is more diverse and consists of thirty-four groups. Despite their sequence diversity, twenty-six residues are conserved in chitinases and endolysins, which can be distinguished by two specific sequence patterns at six and four positions, respectively. Their location outside the catalytic cleft suggests a possible mechanism for substrate specificity that goes beyond the direct interaction with the substrate. The evolution of the GH19 catalytic domain was investigated by large-scale phylogeny. The inferred evolutionary history and putative horizontal gene transfer events differ from previous works. While no clear patterns were detected in endolysins, chitinases varied in sequence length by up to four loop insertions, causing at least eight distinct presence/absence loop combinations. The annotated GH19 sequences and structures are accessible via the GH19 Engineering Database (GH19ED, https://gh19ed.biocatnet.de). The GH19ED has been developed to support the prediction of substrate specificity and the search for novel GH19 enzymes from neglected taxonomic groups or in regions of the sequence space where few sequences have been described yet. Public Library of Science 2021-10-26 /pmc/articles/PMC8547705/ /pubmed/34699529 http://dx.doi.org/10.1371/journal.pone.0256817 Text en © 2021 Orlando et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Orlando, Marco
Buchholz, Patrick C. F.
Lotti, Marina
Pleiss, Jürgen
The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
title The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
title_full The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
title_fullStr The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
title_full_unstemmed The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
title_short The GH19 Engineering Database: Sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
title_sort gh19 engineering database: sequence diversity, substrate scope, and evolution in glycoside hydrolase family 19
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547705/
https://www.ncbi.nlm.nih.gov/pubmed/34699529
http://dx.doi.org/10.1371/journal.pone.0256817
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