TY - JOUR
T1 - Genomics, Exometabolomics, and Metabolic Probing Reveal Conserved Proteolytic Metabolism of Thermoflexus hugenholtzii and Three Candidate Species From China and Japan
AU - Thomas, Scott C.
AU - Payne, Devon
AU - Tamadonfar, Kevin O.
AU - Seymour, Cale O.
AU - Jiao, Jian Yu
AU - Murugapiran, Senthil K.
AU - Lai, Dengxun
AU - Lau, Rebecca
AU - Bowen, Benjamin P.
AU - Silva, Leslie P.
AU - Louie, Katherine B.
AU - Huntemann, Marcel
AU - Clum, Alicia
AU - Spunde, Alex
AU - Pillay, Manoj
AU - Palaniappan, Krishnaveni
AU - Varghese, Neha
AU - Mikhailova, Natalia
AU - Chen, I. Min
AU - Stamatis, Dimitrios
AU - Reddy, T. B.K.
AU - O’Malley, Ronan
AU - Daum, Chris
AU - Shapiro, Nicole
AU - Ivanova, Natalia
AU - Kyrpides, Nikos C.
AU - Woyke, Tanja
AU - Eloe-Fadrosh, Emiley
AU - Hamilton, Trinity L.
AU - Dijkstra, Paul
AU - Dodsworth, Jeremy A.
AU - Northen, Trent R.
AU - Li, Wen Jun
AU - Hedlund, Brian P.
N1 - Publisher Copyright:
© 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.
PY - 2021/5/3
Y1 - 2021/5/3
N2 - Thermoflexus hugenholtzii JAD2T, 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 JAD2T 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 JAD2T 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 13C 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 JAD2T 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 JAD2T using 13C-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 13C-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.
AB - Thermoflexus hugenholtzii JAD2T, 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 JAD2T 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 JAD2T 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 13C 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 JAD2T 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 JAD2T using 13C-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 13C-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.
KW - Chloroflexi
KW - Thermoflexus
KW - Thermoflexus hugenholtzii
KW - exometabolomics
KW - genomics
KW - metagenome-assembled genomes
KW - thermophile
UR - http://www.scopus.com/inward/record.url?scp=85106066387&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85106066387&partnerID=8YFLogxK
U2 - 10.3389/fmicb.2021.632731
DO - 10.3389/fmicb.2021.632731
M3 - Article
AN - SCOPUS:85106066387
SN - 1664-302X
VL - 12
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
M1 - 632731
ER -