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Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1
The hyperthermophilic archaeon Thermococcus onnurineus NA1 has been shown to produce H(2) when using CO, formate, or starch as a growth substrate. This strain can also utilize elemental sulfur as a terminal electron acceptor for heterotrophic growth. To gain insight into sulfur metabolism, the prote...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463584/ https://www.ncbi.nlm.nih.gov/pubmed/25915030 http://dx.doi.org/10.3390/ijms16059167 |
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author | Moon, Yoon-Jung Kwon, Joseph Yun, Sung-Ho Lim, Hye Li Kim, Jonghyun Kim, Soo Jung Kang, Sung Gyun Lee, Jung-Hyun Kim, Seung Il Chung, Young-Ho |
author_facet | Moon, Yoon-Jung Kwon, Joseph Yun, Sung-Ho Lim, Hye Li Kim, Jonghyun Kim, Soo Jung Kang, Sung Gyun Lee, Jung-Hyun Kim, Seung Il Chung, Young-Ho |
author_sort | Moon, Yoon-Jung |
collection | PubMed |
description | The hyperthermophilic archaeon Thermococcus onnurineus NA1 has been shown to produce H(2) when using CO, formate, or starch as a growth substrate. This strain can also utilize elemental sulfur as a terminal electron acceptor for heterotrophic growth. To gain insight into sulfur metabolism, the proteome of T. onnurineus NA1 cells grown under sulfur culture conditions was quantified and compared with those grown under H(2)-evolving substrate culture conditions. Using label-free nano-UPLC-MS(E)-based comparative proteomic analysis, approximately 38.4% of the total identified proteome (589 proteins) was found to be significantly up-regulated (≥1.5-fold) under sulfur culture conditions. Many of these proteins were functionally associated with carbon fixation, Fe–S cluster biogenesis, ATP synthesis, sulfur reduction, protein glycosylation, protein translocation, and formate oxidation. Based on the abundances of the identified proteins in this and other genomic studies, the pathways associated with reductive sulfur metabolism, H(2)-metabolism, and oxidative stress defense were proposed. The results also revealed markedly lower expression levels of enzymes involved in the sulfur assimilation pathway, as well as cysteine desulfurase, under sulfur culture condition. The present results provide the first global atlas of proteome changes triggered by sulfur, and may facilitate an understanding of how hyperthermophilic archaea adapt to sulfur-rich, extreme environments. |
format | Online Article Text |
id | pubmed-4463584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-44635842015-06-16 Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 Moon, Yoon-Jung Kwon, Joseph Yun, Sung-Ho Lim, Hye Li Kim, Jonghyun Kim, Soo Jung Kang, Sung Gyun Lee, Jung-Hyun Kim, Seung Il Chung, Young-Ho Int J Mol Sci Article The hyperthermophilic archaeon Thermococcus onnurineus NA1 has been shown to produce H(2) when using CO, formate, or starch as a growth substrate. This strain can also utilize elemental sulfur as a terminal electron acceptor for heterotrophic growth. To gain insight into sulfur metabolism, the proteome of T. onnurineus NA1 cells grown under sulfur culture conditions was quantified and compared with those grown under H(2)-evolving substrate culture conditions. Using label-free nano-UPLC-MS(E)-based comparative proteomic analysis, approximately 38.4% of the total identified proteome (589 proteins) was found to be significantly up-regulated (≥1.5-fold) under sulfur culture conditions. Many of these proteins were functionally associated with carbon fixation, Fe–S cluster biogenesis, ATP synthesis, sulfur reduction, protein glycosylation, protein translocation, and formate oxidation. Based on the abundances of the identified proteins in this and other genomic studies, the pathways associated with reductive sulfur metabolism, H(2)-metabolism, and oxidative stress defense were proposed. The results also revealed markedly lower expression levels of enzymes involved in the sulfur assimilation pathway, as well as cysteine desulfurase, under sulfur culture condition. The present results provide the first global atlas of proteome changes triggered by sulfur, and may facilitate an understanding of how hyperthermophilic archaea adapt to sulfur-rich, extreme environments. MDPI 2015-04-23 /pmc/articles/PMC4463584/ /pubmed/25915030 http://dx.doi.org/10.3390/ijms16059167 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Moon, Yoon-Jung Kwon, Joseph Yun, Sung-Ho Lim, Hye Li Kim, Jonghyun Kim, Soo Jung Kang, Sung Gyun Lee, Jung-Hyun Kim, Seung Il Chung, Young-Ho Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 |
title | Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 |
title_full | Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 |
title_fullStr | Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 |
title_full_unstemmed | Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 |
title_short | Proteomic Insights into Sulfur Metabolism in the Hydrogen-Producing Hyperthermophilic Archaeon Thermococcus onnurineus NA1 |
title_sort | proteomic insights into sulfur metabolism in the hydrogen-producing hyperthermophilic archaeon thermococcus onnurineus na1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463584/ https://www.ncbi.nlm.nih.gov/pubmed/25915030 http://dx.doi.org/10.3390/ijms16059167 |
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