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Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments

The hyperthermo-piezophilic archaeon Palaeococcus pacificus DY20341(T), isolated from East Pacific hydrothermal sediments, can utilize elemental sulfur as a terminal acceptor to simulate growth. To gain insight into sulfur metabolism, we performed a genomic and transcriptional analysis of Pa. pacifi...

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Autores principales: Zeng, Xiang, Zhang, Xiaobo, Shao, Zongze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981617/
https://www.ncbi.nlm.nih.gov/pubmed/31935923
http://dx.doi.org/10.3390/ijms21010368
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author Zeng, Xiang
Zhang, Xiaobo
Shao, Zongze
author_facet Zeng, Xiang
Zhang, Xiaobo
Shao, Zongze
author_sort Zeng, Xiang
collection PubMed
description The hyperthermo-piezophilic archaeon Palaeococcus pacificus DY20341(T), isolated from East Pacific hydrothermal sediments, can utilize elemental sulfur as a terminal acceptor to simulate growth. To gain insight into sulfur metabolism, we performed a genomic and transcriptional analysis of Pa. pacificus DY20341(T) with/without elemental sulfur as an electron acceptor. In the 2001 protein-coding sequences of the genome, transcriptomic analysis showed that 108 genes increased (by up to 75.1 fold) and 336 genes decreased (by up to 13.9 fold) in the presence of elemental sulfur. Palaeococcus pacificus cultured with elemental sulfur promoted the following: the induction of membrane-bound hydrogenase (MBX), NADH:polysulfide oxidoreductase (NPSOR), NAD(P)H sulfur oxidoreductase (Nsr), sulfide dehydrogenase (SuDH), connected to the sulfur-reducing process, the upregulation of iron and nickel/cobalt transfer, iron–sulfur cluster-carrying proteins (NBP35), and some iron–sulfur cluster-containing proteins (SipA, SAM, CobQ, etc.). The accumulation of metal ions might further impact on regulators, e.g., SurR and TrmB. For growth in proteinous media without elemental sulfur, cells promoted flagelin, peptide/amino acids transporters, and maltose/sugar transporters to upregulate protein and starch/sugar utilization processes and riboflavin and thiamin biosynthesis. This indicates how strain DY20341(T) can adapt to different living conditions with/without elemental sulfur in the hydrothermal fields.
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spelling pubmed-69816172020-02-03 Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments Zeng, Xiang Zhang, Xiaobo Shao, Zongze Int J Mol Sci Article The hyperthermo-piezophilic archaeon Palaeococcus pacificus DY20341(T), isolated from East Pacific hydrothermal sediments, can utilize elemental sulfur as a terminal acceptor to simulate growth. To gain insight into sulfur metabolism, we performed a genomic and transcriptional analysis of Pa. pacificus DY20341(T) with/without elemental sulfur as an electron acceptor. In the 2001 protein-coding sequences of the genome, transcriptomic analysis showed that 108 genes increased (by up to 75.1 fold) and 336 genes decreased (by up to 13.9 fold) in the presence of elemental sulfur. Palaeococcus pacificus cultured with elemental sulfur promoted the following: the induction of membrane-bound hydrogenase (MBX), NADH:polysulfide oxidoreductase (NPSOR), NAD(P)H sulfur oxidoreductase (Nsr), sulfide dehydrogenase (SuDH), connected to the sulfur-reducing process, the upregulation of iron and nickel/cobalt transfer, iron–sulfur cluster-carrying proteins (NBP35), and some iron–sulfur cluster-containing proteins (SipA, SAM, CobQ, etc.). The accumulation of metal ions might further impact on regulators, e.g., SurR and TrmB. For growth in proteinous media without elemental sulfur, cells promoted flagelin, peptide/amino acids transporters, and maltose/sugar transporters to upregulate protein and starch/sugar utilization processes and riboflavin and thiamin biosynthesis. This indicates how strain DY20341(T) can adapt to different living conditions with/without elemental sulfur in the hydrothermal fields. MDPI 2020-01-06 /pmc/articles/PMC6981617/ /pubmed/31935923 http://dx.doi.org/10.3390/ijms21010368 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zeng, Xiang
Zhang, Xiaobo
Shao, Zongze
Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments
title Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments
title_full Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments
title_fullStr Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments
title_full_unstemmed Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments
title_short Metabolic Adaptation to Sulfur of Hyperthermophilic Palaeococcus pacificus DY20341(T) from Deep-Sea Hydrothermal Sediments
title_sort metabolic adaptation to sulfur of hyperthermophilic palaeococcus pacificus dy20341(t) from deep-sea hydrothermal sediments
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6981617/
https://www.ncbi.nlm.nih.gov/pubmed/31935923
http://dx.doi.org/10.3390/ijms21010368
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