Elucidation of sevadicin, a novel non‐ribosomal peptide secondary metabolite produced by the honey bee pathogenic bacterium Paenibacillus larvae
American foulbrood (AFB) caused by the bee pathogenic bacterium Paenibacillus larvae is the most devastating bacterial disease of honey bees worldwide. From AFB‐dead larvae, pure cultures of P. larvae can normally be cultivated indicating that P. larvae is able to defend its niche against all other...
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Published in | Environmental microbiology Vol. 16; no. 5; pp. 1297 - 1309 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Blackwell Science
01.05.2014
Blackwell Publishing Ltd Blackwell Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | American foulbrood (AFB) caused by the bee pathogenic bacterium Paenibacillus larvae is the most devastating bacterial disease of honey bees worldwide. From AFB‐dead larvae, pure cultures of P. larvae can normally be cultivated indicating that P. larvae is able to defend its niche against all other bacteria present. Recently, comparative genome analysis within the species P. larvae suggested the presence of gene clusters coding for multi‐enzyme complexes, such as non‐ribosomal peptide synthetases (NRPSs). The products of these enzyme complexes are known to have a wide range of biological activities including antibacterial activities. We here present our results on antibacterial activity exhibited by vegetative P. larvae and the identification and analysis of a novel antibacterially active P. larvae tripeptide (called sevadicin; Sev) produced by a NRPS encoded by a gene cluster found in the genome of P. larvae. Identification of Sev was ultimately achieved by comparing the secretome of wild‐type P. larvae with knockout mutants of P. larvae lacking production of Sev. Subsequent mass spectrometric studies, enantiomer analytics and chemical synthesis revealed the sequence and configuration of the tripeptide, D‐Phe‐D‐ALa‐Trp, which was shown to have antibacterial activity. The relevance of our findings is discussed in respect to host–pathogen interactions. |
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Bibliography: | http://dx.doi.org/10.1111/1462-2920.12417 German Research Foundation Technische Universität (TU) Berlin istex:EA21AEF738F9F196E13D09147C250963DC01BC22 Brandenburg Fig. S1. Chromatograms and mass spectra of the enantiomeric analysis of the amino acid phenylalanine of Sev by CI(+)-GC/MS: (A) Total ion chromatogram (TIC) of D-Phe standard, tR = 32.0 min. (B) Mass spectrum derived from A (32.0 min). (C) Extracted ion chromatogram (EIC) (m/z 265.5-266.5) from hydrolysed tripeptide [D-amino acids elute first; tR (D-Phe) = 31.8 min; tR (L-Phe) = 32.6 min]. (D) Mass spectrum derived from C (31.8 min). Fig. S2. Chromatograms and mass spectra of the enantiomeric analysis of the amino acid alanine of Sev by CI(+)-GC/MS: (A) Total ion chromatogram (TIC) of D-Ala standard, tR = 8.9 min. (B) Mass spectrum derived from A (8.9 min). (C) Extracted ion chromatogram (EIC) (m/z 235.5-236.5) from hydrolysed tripeptide [D-amino acids elute first; tR (D-Ala) = 8.8 min; tR (L-Ala) = 10.4 min]. (D) Mass spectrum derived from C (8.8 min). Fig. S3. Chromatograms and mass spectra of the enantiomeric analysis of the amino acid tryptophan of Sev by CI(+)-GC/MS: (A) Total ion chromatogram (TIC) of L-Trp standard, tR = 46.0 min. (B) Mass spectrum derived from A (46.0 min). (C) Extracted ion chromatogram (EIC) (m/z 496.5-497.5) from hydrolysed tripeptide. (D) Mass spectrum derived from C (45.8 min). Sachsen-Anhalt, Germany Cluster of Excellence 'Unifying Concepts in Catalysis' (UniCat) ark:/67375/WNG-BH79XJSK-C ArticleID:EMI12417 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1462-2912 1462-2920 |
DOI: | 10.1111/1462-2920.12417 |