Cargando…

Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum

Halobacterium salinarum NRC-1 is an extremophile that grows optimally at 4.3 M NaCl concentration. In spite of being an established model microorganism for the archaea domain, direct comparisons between its proteome and transcriptome during osmotic stress are still not available. Through RNA-seq-bas...

Descripción completa

Detalles Bibliográficos
Autores principales: Onga, Evelyn Ayumi, Vêncio, Ricardo Z. N., Koide, Tie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786353/
https://www.ncbi.nlm.nih.gov/pubmed/36557695
http://dx.doi.org/10.3390/microorganisms10122442
_version_ 1784858272037076992
author Onga, Evelyn Ayumi
Vêncio, Ricardo Z. N.
Koide, Tie
author_facet Onga, Evelyn Ayumi
Vêncio, Ricardo Z. N.
Koide, Tie
author_sort Onga, Evelyn Ayumi
collection PubMed
description Halobacterium salinarum NRC-1 is an extremophile that grows optimally at 4.3 M NaCl concentration. In spite of being an established model microorganism for the archaea domain, direct comparisons between its proteome and transcriptome during osmotic stress are still not available. Through RNA-seq-based transcriptomics, we compared a low salt (2.6 M NaCl) stress condition with 4.3 M of NaCl and found 283 differentially expressed loci. The more commonly found classes of genes were: ABC-type transporters and transcription factors. Similarities, and most importantly, differences between our findings and previously published datasets in similar experimental conditions are discussed. We validated three important biological processes differentially expressed: gas vesicles production (due to down-regulation of gvpA1b, gvpC1b, gvpN1b, and gvpO1b); archaellum formation (due to down-regulation of arlI, arlB1, arlB2, and arlB3); and glycerol metabolism (due to up-regulation of glpA1, glpB, and glpC). Direct comparison between transcriptomics and proteomics showed 58% agreement between mRNA and protein level changes, pointing to post-transcriptional regulation candidates. From those genes, we highlight rpl15e, encoding for the 50S ribosomal protein L15e, for which we hypothesize an ionic strength-dependent conformational change that guides post-transcriptional processing of its mRNA and, thus, possible salt-dependent regulation of the translation machinery.
format Online
Article
Text
id pubmed-9786353
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-97863532022-12-24 Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum Onga, Evelyn Ayumi Vêncio, Ricardo Z. N. Koide, Tie Microorganisms Article Halobacterium salinarum NRC-1 is an extremophile that grows optimally at 4.3 M NaCl concentration. In spite of being an established model microorganism for the archaea domain, direct comparisons between its proteome and transcriptome during osmotic stress are still not available. Through RNA-seq-based transcriptomics, we compared a low salt (2.6 M NaCl) stress condition with 4.3 M of NaCl and found 283 differentially expressed loci. The more commonly found classes of genes were: ABC-type transporters and transcription factors. Similarities, and most importantly, differences between our findings and previously published datasets in similar experimental conditions are discussed. We validated three important biological processes differentially expressed: gas vesicles production (due to down-regulation of gvpA1b, gvpC1b, gvpN1b, and gvpO1b); archaellum formation (due to down-regulation of arlI, arlB1, arlB2, and arlB3); and glycerol metabolism (due to up-regulation of glpA1, glpB, and glpC). Direct comparison between transcriptomics and proteomics showed 58% agreement between mRNA and protein level changes, pointing to post-transcriptional regulation candidates. From those genes, we highlight rpl15e, encoding for the 50S ribosomal protein L15e, for which we hypothesize an ionic strength-dependent conformational change that guides post-transcriptional processing of its mRNA and, thus, possible salt-dependent regulation of the translation machinery. MDPI 2022-12-10 /pmc/articles/PMC9786353/ /pubmed/36557695 http://dx.doi.org/10.3390/microorganisms10122442 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Onga, Evelyn Ayumi
Vêncio, Ricardo Z. N.
Koide, Tie
Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum
title Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum
title_full Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum
title_fullStr Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum
title_full_unstemmed Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum
title_short Low Salt Influences Archaellum-Based Motility, Glycerol Metabolism, and Gas Vesicles Biogenesis in Halobacterium salinarum
title_sort low salt influences archaellum-based motility, glycerol metabolism, and gas vesicles biogenesis in halobacterium salinarum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786353/
https://www.ncbi.nlm.nih.gov/pubmed/36557695
http://dx.doi.org/10.3390/microorganisms10122442
work_keys_str_mv AT ongaevelynayumi lowsaltinfluencesarchaellumbasedmotilityglycerolmetabolismandgasvesiclesbiogenesisinhalobacteriumsalinarum
AT vencioricardozn lowsaltinfluencesarchaellumbasedmotilityglycerolmetabolismandgasvesiclesbiogenesisinhalobacteriumsalinarum
AT koidetie lowsaltinfluencesarchaellumbasedmotilityglycerolmetabolismandgasvesiclesbiogenesisinhalobacteriumsalinarum