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对3-氨基-5-羟基苯甲酸合酶基因进行PCR筛选,可鉴定放线菌中的安莎霉素及与AHBA相关的抗生素产生菌。

PCR screening of 3-amino-5-hydroxybenzoic acid synthase gene leads to identification of ansamycins and AHBA-related antibiotic producers in Actinomycetes.

作者信息

Huitu Z, Linzhuan W, Aiming L, Guizhi S, Feng H, Qiuping L, Yuzhen W, Huanzhang X, Qunjie G, Yiguang W

机构信息

Key Lab of Biotechnology of Antibiotics, Ministry of Health, Institute of Medicinal Biotechnology, CAMS & PUMC, Beijing, China.

出版信息

J Appl Microbiol. 2009 Mar;106(3):755-63. doi: 10.1111/j.1365-2672.2008.04010.x.

Abstract

AIMS

The 3-amino-5-hydroxybenzoic acid (AHBA) synthase is one of the essential and unique enzymes for AHBA biosynthesis. The possibility of screening for ansamycin or AHBA-related antibiotic-producing strains from Actinomycetes by targeting an AHBA synthase gene was explored.

METHODS AND RESULTS

A pair of degenerated primers designed according to the conserved regions of five known AHBA synthases was used to detect AHBA synthase genes within the genomic DNA of Actinomycetes. PCR screening resulted in obtaining 33 AHBA synthase gene-positive strains from 2000 newly isolated Actinomycetes. Phylogenetic analysis of these gene fragments along with those involved in the biosynthesis of structurally determined ansamycins showed that the genes with close phylogenetic relationships might be involved in the biosynthesis of compounds with the same/similar structures. Four strains have been proved to be actual geldanamycin or rifamycin producers by chemical characterization of their fermentation products.

CONCLUSIONS

The results confirmed the feasibility of using the AHBA synthase gene as a probe in polymerase chain reaction (PCR) screening of ansamycin or AHBA-related antibiotic-producing strains.

SIGNIFICANCE AND IMPACT OF THE STUDY

The PCR screening of AHBA synthase gene represents a direct and sensitive molecular method for rapid detection of AHBA-related antibiotic-producing strains.

摘要

目的

3-氨基-5-羟基苯甲酸(AHBA)合酶是AHBA生物合成中必需且独特的酶之一。探讨了通过靶向AHBA合酶基因从放线菌中筛选安莎霉素或AHBA相关抗生素生产菌株的可能性。

方法与结果

根据5种已知AHBA合酶的保守区域设计一对简并引物,用于检测放线菌基因组DNA中的AHBA合酶基因。通过PCR筛选,从2000株新分离的放线菌中获得了33株AHBA合酶基因阳性菌株。对这些基因片段以及参与结构确定的安莎霉素生物合成的基因片段进行系统发育分析表明,具有密切系统发育关系的基因可能参与相同/相似结构化合物的生物合成。通过对4株菌株发酵产物的化学表征,已证明它们是实际的格尔德霉素或利福霉素生产者。

结论

结果证实了在聚合酶链反应(PCR)筛选安莎霉素或AHBA相关抗生素生产菌株中使用AHBA合酶基因作为探针的可行性。

研究的意义和影响

AHBA合酶基因的PCR筛选是一种直接、灵敏的分子方法,可用于快速检测AHBA相关抗生素生产菌株。

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