Stereospecific control of microbial growth by a combinatoric suite of chiral siderophores

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2025-03-03 DOI:10.1073/pnas.2423730122
Parker R. Stow, Kiefer O. Forsch, Emil Thomsen, Hiroaki Naka, Margo G. Haygood, Katherine A. Barbeau, Alison Butler
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Abstract

Bacteria compete for iron by producing small-molecule chelators known as siderophores. The triscatechol siderophores trivanchrobactin and ruckerbactin, produced by Vibrio campbellii DS40M4 and Yersinia ruckeri YRB, respectively, are naturally occurring diastereomers that form chiral ferric complexes in opposing enantiomeric configurations. Chiral recognition is a hallmark of specificity in biological systems, yet the biological consequences of chiral coordination compounds are relatively unexplored. We demonstrate stereoselective discrimination of microbial growth and iron uptake by chiral Fe(III)–siderophores. The siderophore utilization pathway in V. campbellii DS40M4 is stereoselective for Λ-Fe(III)–trivanchrobactin, but not the mismatched Δ-Fe(III)–ruckerbactin diastereomer. Chiral recognition is likely conferred by the stereospecificity of both the outer membrane receptor (OMR) protein FvtA and the periplasmic binding protein (PBP) FvtB, both of which must interact preferentially with the Λ-configured Fe(III)-coordination complexes.
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手性铁载体组合对微生物生长的立体特异性控制
细菌通过产生被称为铁载体的小分子螯合剂来争夺铁。三儿茶酚类铁载体trivanchrobactin和ruckerbactin分别由cambrio cambellii DS40M4和Yersinia ruckerkeri YRB产生,它们是天然存在的非对映体,形成相反对映体构型的手性铁配合物。手性识别是生物系统特异性的标志,但手性配位化合物的生物学后果相对未被探索。我们证明了手性铁(III) -铁载体对微生物生长和铁摄取的立体选择性区分。在campbelllii DS40M4中,铁载体利用途径对Λ-Fe(III) - trivanchbactin具有立体选择性,而对不匹配的Δ-Fe(III) -ruckerbactin非对映体没有立体选择性。手性识别可能是由外膜受体(OMR)蛋白FvtA和质周结合蛋白(PBP) FvtB的立体特异性赋予的,两者都必须优先与Λ-configured Fe(III)-配位复合物相互作用。
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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