Jones G H
J Nat Prod. 1986 Nov-Dec;49(6):981-7. doi: 10.1021/np50048a003.
Phenoxazinone synthase (PHS) is one enzyme that has been implicated in the biosynthesis of actinomycin in Streptomyces antibioticus. The gene for the 88,000 Mr subunit of PHS has been cloned and has been used to study the regulation of the enzyme in S. antibioticus. The expression of the enzyme in growing cultures is regulated at the transcriptional and posttranscriptional levels, and glucose repression of PHS synthesis also involves control at the level of mRNA synthesis. Interestingly, the transformation of S. antibioticus with a multicopy plasmid containing the cloned PHS gene leads to the premature cessation of mycelial growth and actinomycin production. Two other fragments of the S. antibioticus genome have been cloned and these fragments may be involved in the regulation of antibiotic synthesis in the donor organism and in other streptomycetes. These fragments appear to function by activating a normally silent PHS gene in the cloning host employed in these experiments, Streptomyces lividans. The implications of these results are discussed.
吩恶嗪酮合酶(PHS)是一种与抗生链霉菌中放线菌素生物合成有关的酶。PHS 88,000 Mr亚基的基因已被克隆,并已用于研究抗生链霉菌中该酶的调控。该酶在生长培养物中的表达在转录和转录后水平受到调控,并且PHS合成的葡萄糖阻遏也涉及mRNA合成水平的控制。有趣的是,用含有克隆的PHS基因的多拷贝质粒转化抗生链霉菌会导致菌丝体生长和放线菌素产生过早停止。抗生链霉菌基因组的另外两个片段已被克隆,这些片段可能参与供体生物和其他链霉菌中抗生素合成的调控。这些片段似乎通过激活这些实验中使用的克隆宿主——淡紫链霉菌中一个通常沉默的PHS基因来发挥作用。讨论了这些结果的意义。