Sudhakaran V K, Borkar P S
Hindustan Antibiot Bull. 1989 Feb-May;31(1-2):1-14.
Fermentation parameters for the production of penicillin G acylase by Escherichia coli NCIM 2400 have been evaluated. The bacterium produced the enzyme intracellularly when grown in nutrient broth containing PAA. PAA stimulated the enzyme synthesis by 8-10 fold and reduced the lag period. The optimum concentration of PAA for induction was 20 mM and addition of PAA prior to inoculation gave maximum production of PGA. Glucose, lactose, sorbitol, acetate and lactate even at 0.1% concentration catabolically repressed the enzyme formation. Peptone was the best utilised 'N' source for the enzyme production. Phosphate and yeast extract were found to be essential for both the growth and for enzyme biosynthesis. Temperature between 22-24 degrees C was optimum and under ideal condition E. coli NCIM 2400 produced 0.45-0.55 U/ml of penicillin G acylase.
已对大肠杆菌NCIM 2400生产青霉素G酰化酶的发酵参数进行了评估。当该细菌在含有苯乙酸(PAA)的营养肉汤中生长时,会在细胞内产生这种酶。PAA可将酶的合成刺激8至10倍,并缩短延迟期。诱导所需的PAA最佳浓度为20 mM,接种前添加PAA可使青霉素G酰化酶(PGA)产量达到最高。即使浓度仅为0.1%,葡萄糖、乳糖、山梨醇、乙酸盐和乳酸盐也会对酶的形成产生分解代谢阻遏作用。蛋白胨是该酶生产中利用率最高的“氮”源。已发现磷酸盐和酵母提取物对于生长及酶的生物合成均至关重要。22至24摄氏度的温度最为适宜,在理想条件下,大肠杆菌NCIM 2400可产生0.45至0.55 U/ml的青霉素G酰化酶。