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Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes

Viruses are the most abundant and diverse biological entities on the planet and constitute a significant proportion of Earth’s genetic diversity. Most of this diversity is not represented by isolated viral-host systems and has only been observed through sequencing of viral metagenomes (viromes) from...

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Autores principales: Keown, Rachel A., Dums, Jacob T., Brumm, Phillip J., MacDonald, Joyanne, Mead, David A., Ferrell, Barbra D., Moore, Ryan M., Harrison, Amelia O., Polson, Shawn W., Wommack, K. Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069017/
https://www.ncbi.nlm.nih.gov/pubmed/35531281
http://dx.doi.org/10.3389/fmicb.2022.858366
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author Keown, Rachel A.
Dums, Jacob T.
Brumm, Phillip J.
MacDonald, Joyanne
Mead, David A.
Ferrell, Barbra D.
Moore, Ryan M.
Harrison, Amelia O.
Polson, Shawn W.
Wommack, K. Eric
author_facet Keown, Rachel A.
Dums, Jacob T.
Brumm, Phillip J.
MacDonald, Joyanne
Mead, David A.
Ferrell, Barbra D.
Moore, Ryan M.
Harrison, Amelia O.
Polson, Shawn W.
Wommack, K. Eric
author_sort Keown, Rachel A.
collection PubMed
description Viruses are the most abundant and diverse biological entities on the planet and constitute a significant proportion of Earth’s genetic diversity. Most of this diversity is not represented by isolated viral-host systems and has only been observed through sequencing of viral metagenomes (viromes) from environmental samples. Viromes provide snapshots of viral genetic potential, and a wealth of information on viral community ecology. These data also provide opportunities for exploring the biochemistry of novel viral enzymes. The in vitro biochemical characteristics of novel viral DNA polymerases were explored, testing hypothesized differences in polymerase biochemistry according to protein sequence phylogeny. Forty-eight viral DNA Polymerase I (PolA) proteins from estuarine viromes, hot spring metagenomes, and reference viruses, encompassing a broad representation of currently known diversity, were synthesized, expressed, and purified. Novel functionality was shown in multiple PolAs. Intriguingly, some of the estuarine viral polymerases demonstrated moderate to strong innate DNA strand displacement activity at high enzyme concentration. Strand-displacing polymerases have important technological applications where isothermal reactions are desirable. Bioinformatic investigation of genes neighboring these strand displacing polymerases found associations with SNF2 helicase-associated proteins. The specific function of SNF2 family enzymes is unknown for prokaryotes and viruses. In eukaryotes, SNF2 enzymes have chromatin remodeling functions but do not separate nucleic acid strands. This suggests the strand separation function may be fulfilled by the DNA polymerase for viruses carrying SNF2 helicase-associated proteins. Biochemical data elucidated from this study expands understanding of the biology and ecological behavior of unknown viruses. Moreover, given the numerous biotechnological applications of viral DNA polymerases, novel viral polymerases discovered within viromes may be a rich source of biological material for further in vitro DNA amplification advancements.
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spelling pubmed-90690172022-05-05 Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes Keown, Rachel A. Dums, Jacob T. Brumm, Phillip J. MacDonald, Joyanne Mead, David A. Ferrell, Barbra D. Moore, Ryan M. Harrison, Amelia O. Polson, Shawn W. Wommack, K. Eric Front Microbiol Microbiology Viruses are the most abundant and diverse biological entities on the planet and constitute a significant proportion of Earth’s genetic diversity. Most of this diversity is not represented by isolated viral-host systems and has only been observed through sequencing of viral metagenomes (viromes) from environmental samples. Viromes provide snapshots of viral genetic potential, and a wealth of information on viral community ecology. These data also provide opportunities for exploring the biochemistry of novel viral enzymes. The in vitro biochemical characteristics of novel viral DNA polymerases were explored, testing hypothesized differences in polymerase biochemistry according to protein sequence phylogeny. Forty-eight viral DNA Polymerase I (PolA) proteins from estuarine viromes, hot spring metagenomes, and reference viruses, encompassing a broad representation of currently known diversity, were synthesized, expressed, and purified. Novel functionality was shown in multiple PolAs. Intriguingly, some of the estuarine viral polymerases demonstrated moderate to strong innate DNA strand displacement activity at high enzyme concentration. Strand-displacing polymerases have important technological applications where isothermal reactions are desirable. Bioinformatic investigation of genes neighboring these strand displacing polymerases found associations with SNF2 helicase-associated proteins. The specific function of SNF2 family enzymes is unknown for prokaryotes and viruses. In eukaryotes, SNF2 enzymes have chromatin remodeling functions but do not separate nucleic acid strands. This suggests the strand separation function may be fulfilled by the DNA polymerase for viruses carrying SNF2 helicase-associated proteins. Biochemical data elucidated from this study expands understanding of the biology and ecological behavior of unknown viruses. Moreover, given the numerous biotechnological applications of viral DNA polymerases, novel viral polymerases discovered within viromes may be a rich source of biological material for further in vitro DNA amplification advancements. Frontiers Media S.A. 2022-04-21 /pmc/articles/PMC9069017/ /pubmed/35531281 http://dx.doi.org/10.3389/fmicb.2022.858366 Text en Copyright © 2022 Keown, Dums, Brumm, MacDonald, Mead, Ferrell, Moore, Harrison, Polson and Wommack. https://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
Keown, Rachel A.
Dums, Jacob T.
Brumm, Phillip J.
MacDonald, Joyanne
Mead, David A.
Ferrell, Barbra D.
Moore, Ryan M.
Harrison, Amelia O.
Polson, Shawn W.
Wommack, K. Eric
Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes
title Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes
title_full Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes
title_fullStr Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes
title_full_unstemmed Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes
title_short Novel Viral DNA Polymerases From Metagenomes Suggest Genomic Sources of Strand-Displacing Biochemical Phenotypes
title_sort novel viral dna polymerases from metagenomes suggest genomic sources of strand-displacing biochemical phenotypes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069017/
https://www.ncbi.nlm.nih.gov/pubmed/35531281
http://dx.doi.org/10.3389/fmicb.2022.858366
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