Microbiology Section, Department of Molecular Biology, Faculty of Biology and Environmental Sciences, Vegazana Campus, University of León, León, 24071, Spain,
Appl Microbiol Biotechnol. 2013 Nov;97(21):9451-63. doi: 10.1007/s00253-013-5148-7. Epub 2013 Aug 22.
Clusters for clavulanic acid (CA) biosynthesis are present in the actinomycetes Streptomyces flavogriseus ATCC 33331 and Saccharomonospora viridis DSM 43017. These clusters, which are silent, contain blocks of conserved genes in the same order as those of the Streptomyces clavuligerus CA cluster but assembled in a different organization. S. flavogriseus was grown in nine different media, but clavulanic acid production was undetectable using bioassays or by high-performance liquid chromatography analyses. Reverse-transcriptase polymerase chain reaction (RT-PCR) of S. flavogriseus CA biosynthesis genes showed that the regulatory genes ccaR and claR and some biosynthetic genes were expressed whereas expression of cyp, orf12, orf13, and oppA2 was undetectable. The ccaR gene of S. clavuligerus was unable to switch on CA production in S. flavogriseus::[Pfur-ccaR C], but insertion of a cosmid carrying the S. clavuligerus CA cluster (not including the ccaR gene) conferred clavulanic acid production on S. flavogriseus::[SCos-CA] particularly in TBO and YEME media; these results suggests that some of the S. flavogriseus CA genes are inactive. The known heptameric sequences recognized by CcaR in S. clavuligerus are poorly or not conserved in S. flavogriseus. Quantitative RT-PCR analysis of the CA gene clusters of S. clavuligerus and S. flavogriseus showed that the average expression value of the expressed genes in the former strain was in the order of 1.68-fold higher than in the later. The absence of CA production by S. flavogriseus can be traced to the lack of expression of the essential genes cyp, orf12, orf13, orf14, and oppA2. Heterologous expression of S. clavuligerus CA gene cluster in S. flavogriseus::[SCos-CA] was 11- to 14-fold lower than in the parental strain, suggesting that the genetic background of the host strain is important for optimal production of CA in Streptomyces.
产克拉维酸(CA)的簇存在于放线菌灰色链霉菌 ATCC 33331 和绿色糖单孢菌 DSM 43017 中。这些簇是沉默的,包含与棒状链霉菌产 CA 簇相同顺序的保守基因块,但以不同的方式组装。在九种不同的培养基中培养灰色链霉菌,但使用生物测定或高效液相色谱分析都无法检测到克拉维酸的产生。灰色链霉菌 CA 生物合成基因的逆转录聚合酶链反应(RT-PCR)显示,调节基因 ccaR 和 claR 以及一些生物合成基因表达,而 cyp、orf12、orf13 和 oppA2 的表达则无法检测到。棒状链霉菌的 ccaR 基因无法在灰色链霉菌::[Pfur-ccaR C]中开启 CA 生产,但插入携带棒状链霉菌 CA 簇(不包括 ccaR 基因)的 cosmid 赋予灰色链霉菌 CA 生产能力,特别是在 TBO 和 YEME 培养基中;这些结果表明,一些灰色链霉菌 CA 基因是不活跃的。CCA 在棒状链霉菌中识别的已知七聚体序列在灰色链霉菌中保守性较差或不保守。棒状链霉菌和灰色链霉菌 CA 基因簇的定量 RT-PCR 分析表明,前者菌株中表达基因的平均表达值高出后者菌株 1.68 倍。灰色链霉菌不能产生 CA,可以追溯到必需基因 cyp、orf12、orf13、orf14 和 oppA2 的表达缺失。棒状链霉菌 CA 基因簇在灰色链霉菌::[SCos-CA]中的异源表达比在亲本菌株中低 11-14 倍,这表明宿主菌株的遗传背景对链霉菌中 CA 的最佳生产很重要。