Emmert Elizabeth A B, Klimowicz Amy K, Thomas Michael G, Handelsman Jo
Department of Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Appl Environ Microbiol. 2004 Jan;70(1):104-13. doi: 10.1128/AEM.70.1.104-113.2004.
Zwittermicin A represents a new chemical class of antibiotic and has diverse biological activities, including suppression of oomycete diseases of plants and potentiation of the insecticidal activity of Bacillus thuringiensis. To identify genes involved in zwittermicin A production, we generated 4,800 transposon mutants of B. cereus UW101C and screened them for zwittermicin A accumulation. Nine mutants did not produce detectable zwittermicin A, and one mutant produced eightfold more than the parent strain. The DNA flanking the transposon insertions in six of the nine nonproducing mutants contains significant sequence similarity to genes involved in peptide and polyketide antibiotic biosynthesis. The mutant that overproduced zwittermicin A contained a transposon insertion immediately upstream from a gene that encodes a deduced protein that is a member of the MarR family of transcriptional regulators. Three genes identified by the mutant analysis mapped to a region that was previously shown to carry the zwittermicin A self-resistance gene, zmaR, and a biosynthetic gene (E. A. Stohl, J. L. Milner, and J. Handelsman, Gene 237:403-411, 1999). Further sequencing of this region revealed genes proposed to encode zwittermicin A precursor biosynthetic enzymes, in particular, those involved in the formation of the aminomalonyl- and hydroxymalonyl-acyl carrier protein intermediates. Additionally, nonribosomal peptide synthetase (NRPS) and polyketide synthase (PKS) homologs are present, suggesting that zwittermicin A is synthesized by a mixed NRPS/PKS pathway.
两性霉素A代表了一类新型抗生素,具有多种生物学活性,包括抑制植物卵菌病害以及增强苏云金芽孢杆菌的杀虫活性。为了鉴定参与两性霉素A合成的基因,我们构建了蜡状芽孢杆菌UW101C的4800个转座子突变体,并筛选它们的两性霉素A积累情况。9个突变体不产生可检测到的两性霉素A,1个突变体产生的两性霉素A比亲本菌株多8倍。9个不产生两性霉素A的突变体中有6个转座子插入侧翼的DNA与参与肽和聚酮抗生素生物合成的基因具有显著的序列相似性。过量产生两性霉素A的突变体在一个基因的紧邻上游含有一个转座子插入,该基因编码一种推导蛋白,是转录调节因子MarR家族的成员。通过突变体分析鉴定的3个基因定位于一个先前显示携带两性霉素A自身抗性基因zmaR和一个生物合成基因的区域(E. A. Stohl、J. L. Milner和J. Handelsman,《基因》237:403 - 411,1999)。对该区域的进一步测序揭示了推测编码两性霉素A前体生物合成酶的基因,特别是那些参与氨基丙二酰 - 和羟基丙二酰 - 酰基载体蛋白中间体形成的基因。此外,还存在非核糖体肽合成酶(NRPS)和聚酮合成酶(PKS)的同源物,这表明两性霉素A是通过混合的NRPS/PKS途径合成的。