Song Ju Yeon, Kim Eun Sook, Kim Dae Wi, Jensen Susan E, Lee Kye Joon
School of Biological Sciences, Seoul National University, Seoul, 151-747, South Korea.
J Ind Microbiol Biotechnol. 2009 Feb;36(2):301-11. doi: 10.1007/s10295-008-0499-2. Epub 2008 Nov 15.
Three open reading frames denoted as orf21, orf22, and orf23 were identified from downstream of the currently recognized gene cluster for clavulanic acid biosynthesis in Streptomyces clavuligerus ATCC 27064. The new orfs were annotated after in silico analysis as genes encoding a putative sigma factor, a sensor kinase, and a response regulator. The roles of the individual genes were explored by disruption of the corresponding orfs, and the morphological and antibiotic production phenotypes of the resulting mutants were compared. In orf21 and orf22 mutants, no growth or morphological differences were noted, but modest reduction of cephamycin C (orf21), or both cephamycin C and clavulanic acid production (orf22) compared with wild-type, were observed. In orf23 mutant, cell growth and sporulation was retarded, and clavulanic acid and cephamycin C production were reduced to 40 and 47% of wild-type levels, respectively. Conversely, overexpression of orf23 caused precocious hyperproduction of spores on solid medium, and antibiotic production was increased above the levels seen in plasmid control cultures. Transcriptional analyses were also carried out on orf23 and showed that mutation had little effect on transcription of genes associated with the early stages of cephamycin C or clavulanic acid production but transcription of claR, which regulates the late stages of clavulanic acid production, was reduced in orf23 mutants. These observations suggest that the orf23 product may enable S. clavuligerus to respond to environmental changes by altering cell growth and differentiation. In addition, the effects of ORF23 on growth might indirectly regulate the biosynthesis of secondary metabolites such as clavulanic acid and cephamycin C.
从产黄青霉ATCC 27064中目前已知的棒酸生物合成基因簇下游鉴定出三个开放阅读框,分别命名为orf21、orf22和orf23。经过电子分析,这些新的开放阅读框被注释为编码假定的sigma因子、传感器激酶和反应调节因子的基因。通过破坏相应的开放阅读框来探究各个基因的作用,并比较所得突变体的形态和抗生素生产表型。在orf21和orf22突变体中,未观察到生长或形态差异,但与野生型相比,头孢霉素C产量略有降低(orf21),或者头孢霉素C和棒酸产量均降低(orf22)。在orf23突变体中,细胞生长和孢子形成受到抑制,棒酸和头孢霉素C产量分别降至野生型水平的40%和47%。相反,orf23的过表达导致固体培养基上孢子过早过量产生,抗生素产量高于质粒对照培养物中的水平。还对orf23进行了转录分析,结果表明,突变对与头孢霉素C或棒酸生产早期阶段相关的基因转录影响不大,但在orf23突变体中,调节棒酸生产后期阶段的claR转录减少。这些观察结果表明,orf23产物可能使产黄青霉能够通过改变细胞生长和分化来应对环境变化。此外,ORF23对生长的影响可能间接调节次级代谢产物如棒酸和头孢霉素C的生物合成。