A comparative genomics study of genetic products potentially encoding ladderane lipid biosynthesis

Jayne E. Rattray, Marc Strous, Huub J. M. Op den Camp, Stefan Schouten, Mike S. M. Jetten, Jaap S. Sinninghe Damste

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: The fatty acids of anaerobic ammonium oxidizing (anammox) bacteria contain linearly concatenated cyclobutane moieties, so far unique to biology. These moieties are under high ring strain and are synthesised by a presently unknown biosynthetic pathway.Results: Gene clusters encoding enzymes of fatty acid biosynthesis in the anammox bacterium Kuenenia stuttgartiensis and 137 other organisms were analysed and compared in silico to gain further insight into the pathway of (ladderane) fatty acid biosynthesis. In K. stuttgartiensis four large gene clusters encode fatty acid biosynthesis. Next to the regular enzyme complex needed for fatty acid biosynthesis (FASII), the presence of four putative S-adenosyl-methionine (SAM) radical enzymes, two enzymes similar to phytoene desaturases and many divergent paralogues of beta-ketoacyl-ACP synthase (fabF) were unusual. Surprisingly, extensive synteny was observed with FASII gene clusters in the deltaproteobacterium Desulfotalea psychrophila. No ladderane lipids were detected in lipid extracts of this organism but we did find unusual polyunsaturated hydrocarbons (PUHC), not detected in K. stuttgartiensis.Conclusion: We suggest that the unusual gene clusters of K. stuttgartiensis and D. psychrophila encode a novel pathway for anaerobic PUFA biosynthesis and that K. stuttgartiensis further processes PUFA into ladderane lipids, in similar fashion to the previously proposed route of ladderane lipid biosynthesis. However, the presence of divergent paralogues of fabF with radically different active site topologies may suggest an alternative pathway where ladderane moieties are synthesised externally and are recruited into the pathway of fatty acid biosynthesis.Reviewers: This article was reviewed by Dr Michael Galperin (nominated by Prof E. Koonin), Dr Andrei Osterman and Dr Jeremy Selengut.
Original languageEnglish
Article number8
Number of pages16
JournalBiology Direct
Volume4
DOIs
Publication statusPublished - 16 Feb 2009
Externally publishedYes

Funding

We acknowledge the technical assistance of Michiel Kienhuis, Irene Rijpstra and Dr Ellen Hopmans. We would like to thank Dr Stefan Spring, from DSMZ for culturing the D. psychrophila biomass and Dr Marcel van der Meer for discussions on isotopic fractionation. We thank the three reviewers for their constructive criticisms. This study was funded by a grant from the Netherlands Organisation for Scientific Research (NWO) grant no 813.03.002.

FundersFunder number
Nederlandse Organisatie voor Wetenschappelijke Onderzoek (NWO)813.03.002

    Keywords

    • Anaerobic ammonium oxidation
    • Acyl carrier protein
    • Fatty-acid
    • Oxidizing bacteria
    • Escherichia-coli
    • Anammox bacteria
    • Sp-nov.
    • Sequence alignment
    • Marine-sediments
    • Gen. nov.

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