Brakhage A A
Lehrstuhl für Mikrobiologie, Universität München, Germany.
FEMS Microbiol Lett. 1997 Mar 1;148(1):1-10. doi: 10.1111/j.1574-6968.1997.tb10258.x.
The beta-lactam antibiotic penicillin is produced as end product by only some filamentous fungi, most notably by Aspergillus nidulans and Penicillium chrysogenum. The biosynthesis of this secondary metabolite is catalyzed by three enzymes which are encoded by the following three genes: acvA (pcbAB), ipnA (pcbC) and aat (penDE). The genes are organized into a gene cluster. In A. nidulans, several studies have indicated that the genes are controlled by a complex regulatory network. The wide-domain regulatory protein PACC binds to the intergenic region between acvA and ipnA and, at alkaline pH, increases at least ipnA gene transcription. An additional DNA binding protein (PENR1) was suggested to repress acvA and to activate ipnA and aat expression. Furthermore, three recessive trans-acting mutations have been characterized (prgA1, prgB1, npeE1) which most likely correspond to positively acting regulatory genes of the penicillin biosynthesis genes.
β-内酰胺抗生素青霉素仅由一些丝状真菌作为终产物产生,最显著的是构巢曲霉和产黄青霉。这种次级代谢产物的生物合成由三种酶催化,这三种酶由以下三个基因编码:acvA(pcbAB)、ipnA(pcbC)和aat(penDE)。这些基因组成一个基因簇。在构巢曲霉中,多项研究表明这些基因受一个复杂的调控网络控制。广域调控蛋白PACC与acvA和ipnA之间的基因间区域结合,在碱性pH条件下,至少会增加ipnA基因的转录。另一种DNA结合蛋白(PENR1)被认为可抑制acvA并激活ipnA和aat的表达。此外,已鉴定出三种隐性反式作用突变(prgA1、prgB1、npeE1),它们很可能对应于青霉素生物合成基因的正向作用调控基因。