Kilian Ducos, Florence Hakil, Nang Htay Yin, Katarzyna Kinska, Ange Angaïts, Francisco Calderon Celis, Ryszard Lobinski, Sophie Nolivos, Régis Grimaud
{"title":"海洋杆菌SP17的铁载体依赖性和非依赖性铁获取途径","authors":"Kilian Ducos, Florence Hakil, Nang Htay Yin, Katarzyna Kinska, Ange Angaïts, Francisco Calderon Celis, Ryszard Lobinski, Sophie Nolivos, Régis Grimaud","doi":"10.1111/1462-2920.70176","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>We explored the iron acquisition pathways of <i>Marinobacter nauticus</i> SP17, which exhibits distinct growth modes, manifesting as a planktonic population on acetate and forming a biofilm while utilising <i>n</i>-alkanes or triglycerides as substrates. The expression of genes encoding iron-containing proteins and growth yields measured under varying iron concentrations suggest that the balance between iron demand and availability plays a key role in regulating these genes in response to the carbon source and/or growth mode. Phenotypic studies of a petrobactin-deficient mutant revealed that, although this siderophore is important, it is not essential for growth on all substrates under iron-deplete conditions. This suggests the presence of petrobactin-independent iron acquisition pathways. One such pathway involves the ferric ion-binding protein FbpA, as a <i>ΔfbpA</i> mutant exhibits reduced growth on all substrates tested under iron limitation. Notably, the double mutant (Δ<i>asbABF</i> Δ<i>fbpA</i>) failed to grow, demonstrating that petrobactin and FbpA contribute to two distinct major iron acquisition pathways. The siderophore-dependent and -independent pathways appear to be largely functionally redundant and are involved in iron acquisition in all growth modes on all carbon sources tested.</p>\n </div>","PeriodicalId":11898,"journal":{"name":"Environmental microbiology","volume":"27 9","pages":""},"PeriodicalIF":4.0000,"publicationDate":"2025-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Siderophore-Dependent and -Independent Iron Acquisition Pathways in Marinobacter Nauticus SP17\",\"authors\":\"Kilian Ducos, Florence Hakil, Nang Htay Yin, Katarzyna Kinska, Ange Angaïts, Francisco Calderon Celis, Ryszard Lobinski, Sophie Nolivos, Régis Grimaud\",\"doi\":\"10.1111/1462-2920.70176\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>We explored the iron acquisition pathways of <i>Marinobacter nauticus</i> SP17, which exhibits distinct growth modes, manifesting as a planktonic population on acetate and forming a biofilm while utilising <i>n</i>-alkanes or triglycerides as substrates. The expression of genes encoding iron-containing proteins and growth yields measured under varying iron concentrations suggest that the balance between iron demand and availability plays a key role in regulating these genes in response to the carbon source and/or growth mode. Phenotypic studies of a petrobactin-deficient mutant revealed that, although this siderophore is important, it is not essential for growth on all substrates under iron-deplete conditions. This suggests the presence of petrobactin-independent iron acquisition pathways. One such pathway involves the ferric ion-binding protein FbpA, as a <i>ΔfbpA</i> mutant exhibits reduced growth on all substrates tested under iron limitation. Notably, the double mutant (Δ<i>asbABF</i> Δ<i>fbpA</i>) failed to grow, demonstrating that petrobactin and FbpA contribute to two distinct major iron acquisition pathways. The siderophore-dependent and -independent pathways appear to be largely functionally redundant and are involved in iron acquisition in all growth modes on all carbon sources tested.</p>\\n </div>\",\"PeriodicalId\":11898,\"journal\":{\"name\":\"Environmental microbiology\",\"volume\":\"27 9\",\"pages\":\"\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://enviromicro-journals.onlinelibrary.wiley.com/doi/10.1111/1462-2920.70176\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental microbiology","FirstCategoryId":"99","ListUrlMain":"https://enviromicro-journals.onlinelibrary.wiley.com/doi/10.1111/1462-2920.70176","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Siderophore-Dependent and -Independent Iron Acquisition Pathways in Marinobacter Nauticus SP17
We explored the iron acquisition pathways of Marinobacter nauticus SP17, which exhibits distinct growth modes, manifesting as a planktonic population on acetate and forming a biofilm while utilising n-alkanes or triglycerides as substrates. The expression of genes encoding iron-containing proteins and growth yields measured under varying iron concentrations suggest that the balance between iron demand and availability plays a key role in regulating these genes in response to the carbon source and/or growth mode. Phenotypic studies of a petrobactin-deficient mutant revealed that, although this siderophore is important, it is not essential for growth on all substrates under iron-deplete conditions. This suggests the presence of petrobactin-independent iron acquisition pathways. One such pathway involves the ferric ion-binding protein FbpA, as a ΔfbpA mutant exhibits reduced growth on all substrates tested under iron limitation. Notably, the double mutant (ΔasbABF ΔfbpA) failed to grow, demonstrating that petrobactin and FbpA contribute to two distinct major iron acquisition pathways. The siderophore-dependent and -independent pathways appear to be largely functionally redundant and are involved in iron acquisition in all growth modes on all carbon sources tested.
期刊介绍:
Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens