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Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress

Investigating microbial lipid regulation contributes to understanding the lipid-dependent signal transduction process of cells and helps to improve the sensitivity of microorganisms to environmental factors by interfering with lipid metabolism, thus beneficial for constructing advanced cell factorie...

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Autores principales: Sun, Huijie, Cai, Xinghua, Yan, Bing, Bai, Huashan, Meng, Duotao, Mo, Xueyan, He, Sheng, Su, Guijiao, Jiang, Chengjian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792971/
https://www.ncbi.nlm.nih.gov/pubmed/35096014
http://dx.doi.org/10.3389/fgene.2021.798535
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author Sun, Huijie
Cai, Xinghua
Yan, Bing
Bai, Huashan
Meng, Duotao
Mo, Xueyan
He, Sheng
Su, Guijiao
Jiang, Chengjian
author_facet Sun, Huijie
Cai, Xinghua
Yan, Bing
Bai, Huashan
Meng, Duotao
Mo, Xueyan
He, Sheng
Su, Guijiao
Jiang, Chengjian
author_sort Sun, Huijie
collection PubMed
description Investigating microbial lipid regulation contributes to understanding the lipid-dependent signal transduction process of cells and helps to improve the sensitivity of microorganisms to environmental factors by interfering with lipid metabolism, thus beneficial for constructing advanced cell factories of novel molecular drugs. Integrated omics technology was used to systematically reveal the lipid metabolism mechanism of a marine Meyerozyma guilliermondii GXDK6 under high NaCl stress and test the sensitivity of GXDK6 to antibiotics when its lipid metabolism transformed. The omics data showed that when GXDK6 perceived 10% NaCl stress, the expression of AYR1 and NADPH-dependent 1-acyldihydroxyacetone phosphate reductase was inhibited, which weaken the budding and proliferation of cell membranes. This finding was further validated by decreased 64.39% of OD(600) under 10% NaCl stress when compared with salt-free stress. In addition, salt stress promoted a large intracellular accumulation of glycerol, which was also verified by exogenous addition of glycerol. Moreover, NaCl stress remarkably inhibited the expression of drug target proteins (such as lanosterol 14-alpha demethylase), thereby increasing sensitivity to fluconazole. This study provided new insights into the molecular mechanism involved in the regulation of lipid metabolism in Meyerozyma guilliermondii strain and contributed to developing new methods to improve the effectiveness of killing fungi with lower antibiotics.
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spelling pubmed-87929712022-01-28 Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress Sun, Huijie Cai, Xinghua Yan, Bing Bai, Huashan Meng, Duotao Mo, Xueyan He, Sheng Su, Guijiao Jiang, Chengjian Front Genet Genetics Investigating microbial lipid regulation contributes to understanding the lipid-dependent signal transduction process of cells and helps to improve the sensitivity of microorganisms to environmental factors by interfering with lipid metabolism, thus beneficial for constructing advanced cell factories of novel molecular drugs. Integrated omics technology was used to systematically reveal the lipid metabolism mechanism of a marine Meyerozyma guilliermondii GXDK6 under high NaCl stress and test the sensitivity of GXDK6 to antibiotics when its lipid metabolism transformed. The omics data showed that when GXDK6 perceived 10% NaCl stress, the expression of AYR1 and NADPH-dependent 1-acyldihydroxyacetone phosphate reductase was inhibited, which weaken the budding and proliferation of cell membranes. This finding was further validated by decreased 64.39% of OD(600) under 10% NaCl stress when compared with salt-free stress. In addition, salt stress promoted a large intracellular accumulation of glycerol, which was also verified by exogenous addition of glycerol. Moreover, NaCl stress remarkably inhibited the expression of drug target proteins (such as lanosterol 14-alpha demethylase), thereby increasing sensitivity to fluconazole. This study provided new insights into the molecular mechanism involved in the regulation of lipid metabolism in Meyerozyma guilliermondii strain and contributed to developing new methods to improve the effectiveness of killing fungi with lower antibiotics. Frontiers Media S.A. 2022-01-13 /pmc/articles/PMC8792971/ /pubmed/35096014 http://dx.doi.org/10.3389/fgene.2021.798535 Text en Copyright © 2022 Sun, Cai, Yan, Bai, Meng, Mo, He, Su and Jiang. 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 Genetics
Sun, Huijie
Cai, Xinghua
Yan, Bing
Bai, Huashan
Meng, Duotao
Mo, Xueyan
He, Sheng
Su, Guijiao
Jiang, Chengjian
Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress
title Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress
title_full Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress
title_fullStr Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress
title_full_unstemmed Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress
title_short Multi-Omics Analysis of Lipid Metabolism for a Marine Probiotic Meyerozyma guilliermondii GXDK6 Under High NaCl Stress
title_sort multi-omics analysis of lipid metabolism for a marine probiotic meyerozyma guilliermondii gxdk6 under high nacl stress
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8792971/
https://www.ncbi.nlm.nih.gov/pubmed/35096014
http://dx.doi.org/10.3389/fgene.2021.798535
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