A novel in-silico model explores LanM homologs among Hyphomicrobium spp.

IF 5.2 1区 生物学 Q1 BIOLOGY
James J Valdés, Daniel A Petrash, Kurt O Konhauser
{"title":"A novel in-silico model explores LanM homologs among Hyphomicrobium spp.","authors":"James J Valdés, Daniel A Petrash, Kurt O Konhauser","doi":"10.1038/s42003-024-07258-3","DOIUrl":null,"url":null,"abstract":"<p><p>Investigating microorganisms in metal-enriched environments holds the potential to revolutionize the sustainable recovery of critical metals such as lanthanides (Ln<sup>3+</sup>). We observe Hyphomicrobium spp. as part of a Fe<sup>2+</sup>/Mn<sup>2+</sup>-oxidizing consortia native to the ferruginous bottom waters of a Ln<sup>3+</sup>-enriched lake in Czechia. Notably, one species shows similarities to recently discovered bacteria expressing proteins with picomolar Ln<sup>3+</sup> affinity. This finding was substantiated by developing an in-silico ionic competition model and recombinant expression of a homolog protein (Hm-LanM) from Hyphomicrobium methylovorum. Biochemical assays validate Hm-LanM preference for lighter Ln<sup>3+</sup> ions (from lanthanum to gadolinium). This is comparable to established prototypes. Bioinformatics analyses further uncover additional H. methylovorum metabolic biomolecules in genomic proximity to Hm-LanM analogously dependent on Ln<sup>3+</sup>, including an outer membrane receptor that binds Ln<sup>3+</sup>-chelating siderophores. These combined observations underscore the remarkable strategy of Hyphomicrobium spp. for thriving in relatively Ln<sup>3+</sup> enriched zones of metal-polluted environments.</p>","PeriodicalId":10552,"journal":{"name":"Communications Biology","volume":"7 1","pages":"1539"},"PeriodicalIF":5.2000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s42003-024-07258-3","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Investigating microorganisms in metal-enriched environments holds the potential to revolutionize the sustainable recovery of critical metals such as lanthanides (Ln3+). We observe Hyphomicrobium spp. as part of a Fe2+/Mn2+-oxidizing consortia native to the ferruginous bottom waters of a Ln3+-enriched lake in Czechia. Notably, one species shows similarities to recently discovered bacteria expressing proteins with picomolar Ln3+ affinity. This finding was substantiated by developing an in-silico ionic competition model and recombinant expression of a homolog protein (Hm-LanM) from Hyphomicrobium methylovorum. Biochemical assays validate Hm-LanM preference for lighter Ln3+ ions (from lanthanum to gadolinium). This is comparable to established prototypes. Bioinformatics analyses further uncover additional H. methylovorum metabolic biomolecules in genomic proximity to Hm-LanM analogously dependent on Ln3+, including an outer membrane receptor that binds Ln3+-chelating siderophores. These combined observations underscore the remarkable strategy of Hyphomicrobium spp. for thriving in relatively Ln3+ enriched zones of metal-polluted environments.

探索嗜水草菌属中 LanM 同源物的新型内科学模型
对富含金属环境中的微生物进行研究,有可能彻底改变镧系元素(Ln3+)等关键金属的可持续回收。我们观察到 Hyphomicrobium 菌属是捷克一个 Ln3+ 富集湖泊铁锈色底层水域原生的 Fe2+/Mn2+ 氧化联合体的一部分。值得注意的是,其中一个物种与最近发现的表达具有皮摩尔 Ln3+ 亲和力蛋白质的细菌有相似之处。这一发现是通过建立一个硅内离子竞争模型和重组表达来自甲基嗜水性微生物(Hyphomicrobium methylovorum)的同源蛋白(Hm-LanM)而得到证实的。生化检测验证了 Hm-LanM 对较轻的 Ln3+ 离子(从镧到钆)的偏好。这与已建立的原型相当。生物信息学分析进一步发现了 H. methylovorum 在基因组中与 Hm-LanM 相似依赖 Ln3+ 的其他代谢生物大分子,包括结合 Ln3+ 螯合苷元的外膜受体。这些综合观察结果表明,嗜水气单胞菌在金属污染环境中 Ln3+ 相对富集的区域中生长的策略非常出色。
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 求助全文
来源期刊
Communications Biology
Communications Biology Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
1.70%
发文量
1233
审稿时长
13 weeks
期刊介绍: Communications Biology is an open access journal from Nature Research publishing high-quality research, reviews and commentary in all areas of the biological sciences. Research papers published by the journal represent significant advances bringing new biological insight to a specialized area of research.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信