Bhatnagar R K, Doull J L, Vining L C
Biology Department, Dalhousie University, Halifax, N.S., Canada.
Can J Microbiol. 1988 Nov;34(11):1217-23. doi: 10.1139/m88-214.
Both carbon- and nitrogen-limited media that supported a biphasic pattern of growth and chloramphenicol biosynthesis were devised for batch cultures of Streptomyces venezuelae. Where onset of the idiophase was associated with nitrogen depletion, a sharp peak of arylamine synthetase activity coincided with the onset of antibiotic production. The specific activity of the enzyme was highest when the carbon source in the medium was also near depletion at the trophophase-idiophase boundary. In media providing a substantial excess of carbon source through the idiophase, the peak specific activity was reduced by 75%, although the timing of enzyme synthesis was unaltered. Moreover, chemostat cultures in which the growth rate was limited by the glucose concentration in the input medium failed to show a decrease in specific production of chloramphenicol as the steady-state intracellular glucose concentration was increased. The results suggest that a form of "carbon catabolite repression" regulates synthesis of chloramphenicol biosynthetic enzymes during a trophophase-idiophase transition induced by nitrogen starvation. However, this regulatory mechanism does not establish the timing of antibiotic biosynthesis and does not function during nitrogen-sufficient growth in the presence of excess glucose.
我们设计了支持双相生长模式和氯霉素生物合成的碳限制和氮限制培养基,用于委内瑞拉链霉菌的分批培养。在生长分化期的起始与氮耗尽相关的情况下,芳胺合成酶活性的一个尖锐峰值与抗生素产生的起始相吻合。当培养基中的碳源在营养期-生长分化期边界也接近耗尽时,该酶的比活性最高。在整个生长分化期提供大量过量碳源的培养基中,尽管酶合成的时间没有改变,但峰值比活性降低了75%。此外,在恒化器培养中,当输入培养基中的葡萄糖浓度限制生长速率时,随着稳态细胞内葡萄糖浓度的增加,氯霉素的比产量并未显示出下降。结果表明,一种“碳分解代谢物阻遏”形式在氮饥饿诱导的营养期-生长分化期转变过程中调节氯霉素生物合成酶的合成。然而,这种调节机制并不能确定抗生素生物合成的时间,并且在葡萄糖过量存在的氮充足生长过程中不起作用。