Cargando…

Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan

Thermoflexus hugenholtzii JAD2(T), the only cultured representative of the Chloroflexota order Thermoflexales, is abundant in Great Boiling Spring (GBS), NV, United States, and close relatives inhabit geothermal systems globally. However, no defined medium exists for T. hugenholtzii JAD2(T) and no s...

Descripción completa

Detalles Bibliográficos
Autores principales: Thomas, Scott C., Payne, Devon, Tamadonfar, Kevin O., Seymour, Cale O., Jiao, Jian-Yu, Murugapiran, Senthil K., Lai, Dengxun, Lau, Rebecca, Bowen, Benjamin P., Silva, Leslie P., Louie, Katherine B., Huntemann, Marcel, Clum, Alicia, Spunde, Alex, Pillay, Manoj, Palaniappan, Krishnaveni, Varghese, Neha, Mikhailova, Natalia, Chen, I-Min, Stamatis, Dimitrios, Reddy, T. B. K., O’Malley, Ronan, Daum, Chris, Shapiro, Nicole, Ivanova, Natalia, Kyrpides, Nikos C., Woyke, Tanja, Eloe-Fadrosh, Emiley, Hamilton, Trinity L., Dijkstra, Paul, Dodsworth, Jeremy A., Northen, Trent R., Li, Wen-Jun, Hedlund, Brian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129789/
https://www.ncbi.nlm.nih.gov/pubmed/34017316
http://dx.doi.org/10.3389/fmicb.2021.632731
_version_ 1783694379770183680
author Thomas, Scott C.
Payne, Devon
Tamadonfar, Kevin O.
Seymour, Cale O.
Jiao, Jian-Yu
Murugapiran, Senthil K.
Lai, Dengxun
Lau, Rebecca
Bowen, Benjamin P.
Silva, Leslie P.
Louie, Katherine B.
Huntemann, Marcel
Clum, Alicia
Spunde, Alex
Pillay, Manoj
Palaniappan, Krishnaveni
Varghese, Neha
Mikhailova, Natalia
Chen, I-Min
Stamatis, Dimitrios
Reddy, T. B. K.
O’Malley, Ronan
Daum, Chris
Shapiro, Nicole
Ivanova, Natalia
Kyrpides, Nikos C.
Woyke, Tanja
Eloe-Fadrosh, Emiley
Hamilton, Trinity L.
Dijkstra, Paul
Dodsworth, Jeremy A.
Northen, Trent R.
Li, Wen-Jun
Hedlund, Brian P.
author_facet Thomas, Scott C.
Payne, Devon
Tamadonfar, Kevin O.
Seymour, Cale O.
Jiao, Jian-Yu
Murugapiran, Senthil K.
Lai, Dengxun
Lau, Rebecca
Bowen, Benjamin P.
Silva, Leslie P.
Louie, Katherine B.
Huntemann, Marcel
Clum, Alicia
Spunde, Alex
Pillay, Manoj
Palaniappan, Krishnaveni
Varghese, Neha
Mikhailova, Natalia
Chen, I-Min
Stamatis, Dimitrios
Reddy, T. B. K.
O’Malley, Ronan
Daum, Chris
Shapiro, Nicole
Ivanova, Natalia
Kyrpides, Nikos C.
Woyke, Tanja
Eloe-Fadrosh, Emiley
Hamilton, Trinity L.
Dijkstra, Paul
Dodsworth, Jeremy A.
Northen, Trent R.
Li, Wen-Jun
Hedlund, Brian P.
author_sort Thomas, Scott C.
collection PubMed
description Thermoflexus hugenholtzii JAD2(T), the only cultured representative of the Chloroflexota order Thermoflexales, is abundant in Great Boiling Spring (GBS), NV, United States, and close relatives inhabit geothermal systems globally. However, no defined medium exists for T. hugenholtzii JAD2(T) and no single carbon source is known to support its growth, leaving key knowledge gaps in its metabolism and nutritional needs. Here, we report comparative genomic analysis of the draft genome of T. hugenholtzii JAD2(T) and eight closely related metagenome-assembled genomes (MAGs) from geothermal sites in China, Japan, and the United States, representing “Candidatus Thermoflexus japonica,” “Candidatus Thermoflexus tengchongensis,” and “Candidatus Thermoflexus sinensis.” Genomics was integrated with targeted exometabolomics and (13)C metabolic probing of T. hugenholtzii. The Thermoflexus genomes each code for complete central carbon metabolic pathways and an unusually high abundance and diversity of peptidases, particularly Metallo- and Serine peptidase families, along with ABC transporters for peptides and some amino acids. The T. hugenholtzii JAD2(T) exometabolome provided evidence of extracellular proteolytic activity based on the accumulation of free amino acids. However, several neutral and polar amino acids appear not to be utilized, based on their accumulation in the medium and the lack of annotated transporters. Adenine and adenosine were scavenged, and thymine and nicotinic acid were released, suggesting interdependency with other organisms in situ. Metabolic probing of T. hugenholtzii JAD2(T) using (13)C-labeled compounds provided evidence of oxidation of glucose, pyruvate, cysteine, and citrate, and functioning glycolytic, tricarboxylic acid (TCA), and oxidative pentose-phosphate pathways (PPPs). However, differential use of position-specific (13)C-labeled compounds showed that glycolysis and the TCA cycle were uncoupled. Thus, despite the high abundance of Thermoflexus in sediments of some geothermal systems, they appear to be highly focused on chemoorganotrophy, particularly protein degradation, and may interact extensively with other microorganisms in situ.
format Online
Article
Text
id pubmed-8129789
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-81297892021-05-19 Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan Thomas, Scott C. Payne, Devon Tamadonfar, Kevin O. Seymour, Cale O. Jiao, Jian-Yu Murugapiran, Senthil K. Lai, Dengxun Lau, Rebecca Bowen, Benjamin P. Silva, Leslie P. Louie, Katherine B. Huntemann, Marcel Clum, Alicia Spunde, Alex Pillay, Manoj Palaniappan, Krishnaveni Varghese, Neha Mikhailova, Natalia Chen, I-Min Stamatis, Dimitrios Reddy, T. B. K. O’Malley, Ronan Daum, Chris Shapiro, Nicole Ivanova, Natalia Kyrpides, Nikos C. Woyke, Tanja Eloe-Fadrosh, Emiley Hamilton, Trinity L. Dijkstra, Paul Dodsworth, Jeremy A. Northen, Trent R. Li, Wen-Jun Hedlund, Brian P. Front Microbiol Microbiology Thermoflexus hugenholtzii JAD2(T), the only cultured representative of the Chloroflexota order Thermoflexales, is abundant in Great Boiling Spring (GBS), NV, United States, and close relatives inhabit geothermal systems globally. However, no defined medium exists for T. hugenholtzii JAD2(T) and no single carbon source is known to support its growth, leaving key knowledge gaps in its metabolism and nutritional needs. Here, we report comparative genomic analysis of the draft genome of T. hugenholtzii JAD2(T) and eight closely related metagenome-assembled genomes (MAGs) from geothermal sites in China, Japan, and the United States, representing “Candidatus Thermoflexus japonica,” “Candidatus Thermoflexus tengchongensis,” and “Candidatus Thermoflexus sinensis.” Genomics was integrated with targeted exometabolomics and (13)C metabolic probing of T. hugenholtzii. The Thermoflexus genomes each code for complete central carbon metabolic pathways and an unusually high abundance and diversity of peptidases, particularly Metallo- and Serine peptidase families, along with ABC transporters for peptides and some amino acids. The T. hugenholtzii JAD2(T) exometabolome provided evidence of extracellular proteolytic activity based on the accumulation of free amino acids. However, several neutral and polar amino acids appear not to be utilized, based on their accumulation in the medium and the lack of annotated transporters. Adenine and adenosine were scavenged, and thymine and nicotinic acid were released, suggesting interdependency with other organisms in situ. Metabolic probing of T. hugenholtzii JAD2(T) using (13)C-labeled compounds provided evidence of oxidation of glucose, pyruvate, cysteine, and citrate, and functioning glycolytic, tricarboxylic acid (TCA), and oxidative pentose-phosphate pathways (PPPs). However, differential use of position-specific (13)C-labeled compounds showed that glycolysis and the TCA cycle were uncoupled. Thus, despite the high abundance of Thermoflexus in sediments of some geothermal systems, they appear to be highly focused on chemoorganotrophy, particularly protein degradation, and may interact extensively with other microorganisms in situ. Frontiers Media S.A. 2021-05-03 /pmc/articles/PMC8129789/ /pubmed/34017316 http://dx.doi.org/10.3389/fmicb.2021.632731 Text en Copyright © 2021 Thomas, Payne, Tamadonfar, Seymour, Jiao, Murugapiran, Lai, Lau, Bowen, Silva, Louie, Huntemann, Clum, Spunde, Pillay, Palaniappan, Varghese, Mikhailova, Chen, Stamatis, Reddy, O’Malley, Daum, Shapiro, Ivanova, Kyrpides, Woyke, Eloe-Fadrosh, Hamilton, Dijkstra, Dodsworth, Northen, Li and Hedlund. 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
Thomas, Scott C.
Payne, Devon
Tamadonfar, Kevin O.
Seymour, Cale O.
Jiao, Jian-Yu
Murugapiran, Senthil K.
Lai, Dengxun
Lau, Rebecca
Bowen, Benjamin P.
Silva, Leslie P.
Louie, Katherine B.
Huntemann, Marcel
Clum, Alicia
Spunde, Alex
Pillay, Manoj
Palaniappan, Krishnaveni
Varghese, Neha
Mikhailova, Natalia
Chen, I-Min
Stamatis, Dimitrios
Reddy, T. B. K.
O’Malley, Ronan
Daum, Chris
Shapiro, Nicole
Ivanova, Natalia
Kyrpides, Nikos C.
Woyke, Tanja
Eloe-Fadrosh, Emiley
Hamilton, Trinity L.
Dijkstra, Paul
Dodsworth, Jeremy A.
Northen, Trent R.
Li, Wen-Jun
Hedlund, Brian P.
Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
title Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
title_full Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
title_fullStr Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
title_full_unstemmed Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
title_short Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
title_sort genomics, exometabolomics, and metabolic probing reveal conserved proteolytic metabolism of thermoflexus hugenholtzii and three candidate species from china and japan
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8129789/
https://www.ncbi.nlm.nih.gov/pubmed/34017316
http://dx.doi.org/10.3389/fmicb.2021.632731
work_keys_str_mv AT thomasscottc genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT paynedevon genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT tamadonfarkevino genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT seymourcaleo genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT jiaojianyu genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT murugapiransenthilk genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT laidengxun genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT laurebecca genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT bowenbenjaminp genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT silvalesliep genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT louiekatherineb genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT huntemannmarcel genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT clumalicia genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT spundealex genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT pillaymanoj genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT palaniappankrishnaveni genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT vargheseneha genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT mikhailovanatalia genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT chenimin genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT stamatisdimitrios genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT reddytbk genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT omalleyronan genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT daumchris genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT shapironicole genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT ivanovanatalia genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT kyrpidesnikosc genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT woyketanja genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT eloefadroshemiley genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT hamiltontrinityl genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT dijkstrapaul genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT dodsworthjeremya genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT northentrentr genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT liwenjun genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan
AT hedlundbrianp genomicsexometabolomicsandmetabolicprobingrevealconservedproteolyticmetabolismofthermoflexushugenholtziiandthreecandidatespeciesfromchinaandjapan