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唾液乳链菌肽G32,一种原型化脓性链球菌类乳链菌肽SA-FF22的同源物,由共生菌唾液链球菌产生。

Salivaricin G32, a Homolog of the Prototype Streptococcus pyogenes Nisin-Like Lantibiotic SA-FF22, Produced by the Commensal Species Streptococcus salivarius.

作者信息

Wescombe Philip A, Dyet Kristin H, Dierksen Karen P, Power Daniel A, Jack Ralph W, Burton Jeremy P, Inglis Megan A, Wescombe Anna L, Tagg John R

机构信息

BLIS Technologies Ltd., Centre for Innovation, University of Otago, P.O. Box 56, Dunedin 9054, New Zealand.

出版信息

Int J Microbiol. 2012;2012:738503. doi: 10.1155/2012/738503. Epub 2012 Apr 8.

DOI:10.1155/2012/738503
PMID:22567013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3332205/
Abstract

Salivaricin G32, a 2667 Da novel member of the SA-FF22 cluster of lantibiotics, has been purified and characterized from Streptococcus salivarius strain G32. The inhibitory peptide differs from the Streptococcus pyogenes-produced SA-FF22 in the absence of lysine in position 2. The salivaricin G32 locus was widely distributed in BLIS-producing S. salivarius, with 6 (23%) of 26 strains PCR-positive for the structural gene, slnA. As for most other lantibiotics produced by S. salivarius, the salivaricin G32 locus can be megaplasmid encoded. Another member of the SA-FF22 family was detected in two Streptococcus dysgalactiae of bovine origin, an observation supportive of widespread distribution of this lantibiotic within the genus Streptococcus. Since the inhibitory spectrum of salivaricin G32 includes Streptococcus pyogenes, its production by S. salivarius, either as a member of the normal oral microflora or as a commercial probiotic, could serve to enhance protection of the human host against S. pyogenes infection.

摘要

唾液乳链菌肽G32是羊毛硫抗生素SA - FF22簇的一个分子量为2667Da的新成员,已从唾液链球菌G32菌株中纯化并鉴定。该抑制性肽与化脓性链球菌产生的SA - FF22的不同之处在于第2位没有赖氨酸。唾液乳链菌肽G32基因座在产生细菌素的唾液链球菌中广泛分布,26株中有6株(23%)对结构基因slnA进行PCR检测呈阳性。与唾液链球菌产生的大多数其他羊毛硫抗生素一样,唾液乳链菌肽G32基因座可由大质粒编码。在两株牛源停乳链球菌中检测到SA - FF22家族的另一个成员,这一观察结果支持了这种羊毛硫抗生素在链球菌属内广泛分布。由于唾液乳链菌肽G32的抑制谱包括化脓性链球菌,唾液链球菌作为正常口腔微生物群的一员或作为商业益生菌产生该物质,可增强人类宿主对化脓性链球菌感染的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/0d96902015f4/IJMB2012-738503.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/b8d5b3acdf5a/IJMB2012-738503.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/95a5be6c2456/IJMB2012-738503.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/858611944077/IJMB2012-738503.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/0d96902015f4/IJMB2012-738503.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/b8d5b3acdf5a/IJMB2012-738503.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/95a5be6c2456/IJMB2012-738503.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/858611944077/IJMB2012-738503.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65d/3332205/0d96902015f4/IJMB2012-738503.004.jpg

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