Gonsior Melanie, Mühlenweg Agnes, Tietzmann Marcel, Rausch Saskia, Poch Annette, Süssmuth Roderich D
Institut für Chemie, Technische Universität BerlinStrasse des 17. Juni 124, 10623, Berlin, Germany.
Chembiochem. 2015 Dec;16(18):2610-4. doi: 10.1002/cbic.201500432. Epub 2015 Oct 30.
Feglymycin, a peptide antibiotic produced by Streptomyces sp. DSM 11171, consists mostly of nonproteinogenic phenylglycine-type amino acids. It possesses antibacterial activity against methicillin-resistant Staphylococcus aureus strains and antiviral activity against HIV. Inhibition of the early steps of bacterial peptidoglycan synthesis indicated a mode of action different from those of other peptide antibiotics. Here we describe the identification and assignment of the feglymycin (feg) biosynthesis gene cluster, which codes for a 13-module nonribosomal peptide synthetase (NRPS) system. Inactivation of an NRPS gene and supplementation of a hydroxymandelate oxidase mutant with the amino acid l-Hpg proved the identity of the feg cluster. Feeding of Hpg-related unnatural amino acids was not successful. This characterization of the feg cluster is an important step to understanding the biosynthesis of this potent antibacterial peptide.
费格霉素是由链霉菌DSM 11171产生的一种肽类抗生素,主要由非蛋白质ogenic苯甘氨酸型氨基酸组成。它对耐甲氧西林金黄色葡萄球菌菌株具有抗菌活性,对HIV具有抗病毒活性。对细菌肽聚糖合成早期步骤的抑制表明其作用方式与其他肽类抗生素不同。在此,我们描述了费格霉素(feg)生物合成基因簇的鉴定和分配,该基因簇编码一个13模块的非核糖体肽合成酶(NRPS)系统。一个NRPS基因的失活以及用氨基酸l-Hpg补充羟基扁桃酸氧化酶突变体证明了feg簇的身份。用与Hpg相关的非天然氨基酸进行喂养未成功。feg簇的这一特征描述是理解这种强效抗菌肽生物合成的重要一步。