Klein C, Entian K D
Institute for Microbiology, Biozentrum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Federal Republic of Germany.
Appl Environ Microbiol. 1994 Aug;60(8):2793-801. doi: 10.1128/aem.60.8.2793-2801.1994.
Subtilin is a ribosomally synthesized peptide antibiotic produced by Bacillus subtilis ATCC 6633. Recently, we reported regarding genes spaB, spaT, and spaC (C. Klein, C. Kaletta, N. Schnell, and K.-D. Entian, Appl. Environ. Microbiol. 58:132-142, 1992) which are involved in the biosynthesis of subtilin, and genes spaR and spaK (C. Klein, C. Kaletta, and K.-D. Entian, Appl. Environ. Microbiol. 59:296-303, 1993), which regulate subtilin biosynthesis via a histidine kinase/response regulator system. Further sequence analysis revealed the presence of three additional open reading frames, spaI, spaF, and spaG, downstream of the structural gene spaS. The spaI gene encodes a hydrophilic 19.3-kDa lipoprotein containing a consensus signal sequence, indicating that this protein might be membrane anchored. A similar gene, nisI, has been identified in the nisin producer. SpaF shows strong homology to members of the family of ABC transporters. spaG encodes a hydrophobic protein which might form the active transporter together with SpaF. Gene disruption mutants in all three genes were still able to produce subtilin; however, these mutants were more sensitive to subtilin than the wild-type strain. These results show that these genes are involved in the immunity mechanism of the producer strain. A similar involvement of an ABC transporter in the self-protection mechanism has been described for the McbE and McbF transporter, which confers immunity against microcin B17 in Escherichia coli. Mutants containing mutations in the genes spaR and spaK, which are responsible for regulation of subtilin biosynthesis, also became more sensitive to subtilin.(ABSTRACT TRUNCATED AT 250 WORDS)
枯草菌素是由枯草芽孢杆菌ATCC 6633产生的一种核糖体合成的肽抗生素。最近,我们报道了参与枯草菌素生物合成的基因spaB、spaT和spaC(C. 克莱因、C. 卡莱塔、N. 施内尔和K.-D. 恩蒂安,《应用与环境微生物学》58:132 - 142,1992年),以及通过组氨酸激酶/应答调节系统调节枯草菌素生物合成的基因spaR和spaK(C. 克莱因、C. 卡莱塔和K.-D. 恩蒂安,《应用与环境微生物学》59:296 - 303,1993年)。进一步的序列分析显示,在结构基因spaS的下游存在另外三个开放阅读框,即spaI、spaF和spaG。spaI基因编码一种含有共有信号序列的亲水性19.3 kDa脂蛋白,这表明该蛋白可能锚定在膜上。在乳链菌肽产生菌中已鉴定出一个类似的基因nisI。SpaF与ABC转运蛋白家族的成员具有很强的同源性。spaG编码一种疏水蛋白,它可能与SpaF一起形成活性转运蛋白。这三个基因的基因破坏突变体仍然能够产生枯草菌素;然而,这些突变体比野生型菌株对枯草菌素更敏感。这些结果表明这些基因参与了产生菌的免疫机制。对于赋予大肠杆菌对微菌素B17免疫的McbE和McbF转运蛋白,已描述了ABC转运蛋白在自我保护机制中的类似参与情况。在负责枯草菌素生物合成调节的基因spaR和spaK中含有突变的突变体对枯草菌素也变得更敏感。(摘要截短至250字)