Physiological and genomic insights into abiotic stress of halophilic archaeon Natrinema altunense 4.1R isolated from a saline ecosystem of Tunisian desert.

IF 1.3 4区 生物学 Q4 GENETICS & HEREDITY Genetica Pub Date : 2023-04-01 DOI:10.1007/s10709-023-00182-0
Afef Najjari, Ayoub Boussetta, Noha Youssef, Javier A Linares-Pastén, Mouna Mahjoubi, Rahma Belloum, Haitham Sghaier, Ameur Cherif, Hadda Imene Ouzari
{"title":"Physiological and genomic insights into abiotic stress of halophilic archaeon Natrinema altunense 4.1R isolated from a saline ecosystem of Tunisian desert.","authors":"Afef Najjari,&nbsp;Ayoub Boussetta,&nbsp;Noha Youssef,&nbsp;Javier A Linares-Pastén,&nbsp;Mouna Mahjoubi,&nbsp;Rahma Belloum,&nbsp;Haitham Sghaier,&nbsp;Ameur Cherif,&nbsp;Hadda Imene Ouzari","doi":"10.1007/s10709-023-00182-0","DOIUrl":null,"url":null,"abstract":"<p><p>Halophilic archaea are polyextremophiles with the ability to withstand fluctuations in salinity, high levels of ultraviolet radiation, and oxidative stress, allowing them to survive in a wide range of environments and making them an excellent model for astrobiological research. Natrinema altunense 4.1R is a halophilic archaeon isolated from the endorheic saline lake systems, Sebkhas, located in arid and semi-arid regions of Tunisia. It is an ecosystem characterized by periodic flooding from subsurface groundwater and fluctuating salinities. Here, we assess the physiological responses and genomic characterization of N. altunense 4.1R to UV-C radiation, as well as osmotic and oxidative stresses. Results showed that the 4.1R strain is able to survive up to 36% of salinity, up to 180 J/m<sup>2</sup> to UV-C radiation, and at 50 mM of H<sub>2</sub>O<sub>2</sub>, a resistance profile similar to Halobacterium salinarum, a strain often used as UV-C resistant model. In order to understand the genetic determinants of N. altunense 4.1R survival strategy, we sequenced and analyzed its genome. Results showed multiple gene copies of osmotic stress, oxidative stress, and DNA repair response mechanisms supporting its survivability at extreme salinities and radiations. Indeed, the 3D molecular structures of seven proteins related to responses to UV-C radiation (excinucleases UvrA, UvrB, and UvrC, and photolyase), saline stress (trehalose-6-phosphate synthase OtsA and trehalose-phosphatase OtsB), and oxidative stress (superoxide dismutase SOD) were constructed by homology modeling. This study extends the abiotic stress range for the species N. altunense and adds to the repertoire of UV and oxidative stress resistance genes generally known from haloarchaeon.</p>","PeriodicalId":55121,"journal":{"name":"Genetica","volume":"151 2","pages":"133-152"},"PeriodicalIF":1.3000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995536/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetica","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10709-023-00182-0","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Halophilic archaea are polyextremophiles with the ability to withstand fluctuations in salinity, high levels of ultraviolet radiation, and oxidative stress, allowing them to survive in a wide range of environments and making them an excellent model for astrobiological research. Natrinema altunense 4.1R is a halophilic archaeon isolated from the endorheic saline lake systems, Sebkhas, located in arid and semi-arid regions of Tunisia. It is an ecosystem characterized by periodic flooding from subsurface groundwater and fluctuating salinities. Here, we assess the physiological responses and genomic characterization of N. altunense 4.1R to UV-C radiation, as well as osmotic and oxidative stresses. Results showed that the 4.1R strain is able to survive up to 36% of salinity, up to 180 J/m2 to UV-C radiation, and at 50 mM of H2O2, a resistance profile similar to Halobacterium salinarum, a strain often used as UV-C resistant model. In order to understand the genetic determinants of N. altunense 4.1R survival strategy, we sequenced and analyzed its genome. Results showed multiple gene copies of osmotic stress, oxidative stress, and DNA repair response mechanisms supporting its survivability at extreme salinities and radiations. Indeed, the 3D molecular structures of seven proteins related to responses to UV-C radiation (excinucleases UvrA, UvrB, and UvrC, and photolyase), saline stress (trehalose-6-phosphate synthase OtsA and trehalose-phosphatase OtsB), and oxidative stress (superoxide dismutase SOD) were constructed by homology modeling. This study extends the abiotic stress range for the species N. altunense and adds to the repertoire of UV and oxidative stress resistance genes generally known from haloarchaeon.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
从突尼斯沙漠盐生态系统分离的嗜盐古菌Natrinema altunense 4.1R的非生物胁迫的生理和基因组学见解
嗜盐古菌是多极端微生物,具有承受盐度波动、高水平紫外线辐射和氧化应激的能力,使它们能够在各种环境中生存,并使它们成为天体生物学研究的绝佳模型。Natrinema altunense 4.1R是一种嗜盐古菌,分离自位于突尼斯干旱和半干旱地区的内源性盐湖系统Sebkhas。它是一个以地下地下水周期性洪水和盐度波动为特征的生态系统。在这里,我们评估了N. altunense 4.1R对UV-C辐射以及渗透和氧化应激的生理反应和基因组特征。结果表明,4.1R菌株在36%的盐度、180j /m2的UV-C辐射和50mm的H2O2条件下均能存活,其抗性谱与常用的耐UV-C模型盐盐杆菌相似。为了进一步了解南褐蝽4.1R生存策略的遗传决定因素,我们对其基因组进行了测序和分析。结果表明,渗透胁迫、氧化应激和DNA修复反应机制的多个基因拷贝支持其在极端盐度和辐射下的生存能力。事实上,通过同源性建模,构建了7种与UV-C辐射反应相关的蛋白(切酶UvrA、UvrB、UvrC和光解酶)、盐胁迫(海藻糖-6-磷酸合成酶OtsA和海藻糖-磷酸酶OtsB)和氧化应激(超氧化物歧化酶SOD)的三维分子结构。该研究扩大了N. altunense物种的非生物胁迫范围,并增加了通常从盐古菌中已知的抗紫外线和氧化应激基因库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Genetica
Genetica 生物-遗传学
CiteScore
2.70
自引率
0.00%
发文量
32
审稿时长
>12 weeks
期刊介绍: Genetica publishes papers dealing with genetics, genomics, and evolution. Our journal covers novel advances in the fields of genomics, conservation genetics, genotype-phenotype interactions, evo-devo, population and quantitative genetics, and biodiversity. Genetica publishes original research articles addressing novel conceptual, experimental, and theoretical issues in these areas, whatever the taxon considered. Biomedical papers and papers on breeding animal and plant genetics are not within the scope of Genetica, unless framed in an evolutionary context. Recent advances in genetics, genomics and evolution are also published in thematic issues and synthesis papers published by experts in the field.
期刊最新文献
Genome-wide identification and data mining reveals major-latex protein (MLP) from the PR-10 protein family played defense-related roles against phytopathogenic challenges in cassava (Manihot esculenta Crantz). Comparative assessment of genotyping-by-sequencing and whole-exome sequencing for estimating genetic diversity and geographic structure in small sample sizes: insights from wild jaguar populations. Phylogenetic exploration, codon usage bias, and genomic divergence in Hydrocotyle: a comparative plastome study across different geographical locations. Identification of bHLH transcription factors and screening of anthocyanin-related genes in Lagerstroemia indica. Systematic analysis of the ARF gene family in Fagopyrum dibotrys and its potential roles in stress tolerance.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1