Sharon C, Nakazato M, Ogawa H I, Kato Y
Dept. of Applied Chemistry, Kyushu Institute of Technology, Kitakyushu-shi, Japan.
Indian J Exp Biol. 1999 May;37(5):481-6.
A highly stable lipase from Pseudomonas aeruginosa KKA-5 was produced by batch cultivation technique employing shake flask and 5 L-bioreactor. The bioreactor was run at different airflow rates. Low airflow rates (1 and 3 L/min), did not lead to effective growth and lipase production. Growth increased by about one order and lipase production increased by about 6 times, at an airflow rate of 5 L/min. Lipase production occurred during decelerated cell growth. A highly stable lipase was produced which retained its activity in the running bioreactor, even after a period of one month. This stable lipase was partially-purified using ammonium sulphate precipitation technique. Castor oil was hydrolyzed using 300U crude and partially-purified lipase, each. Approximately 21-fold, partially-purified lipase could hydrolyze 81% castor oil within a period of 96 hr, where as only 63% hydrolysis was obtained, in 216 hour, when crude lipase was used.
采用摇瓶和5升生物反应器的分批培养技术,生产了一种来自铜绿假单胞菌KKA-5的高度稳定的脂肪酶。生物反应器在不同的气流速率下运行。低气流速率(1和3升/分钟)不会导致有效的生长和脂肪酶产生。在气流速率为5升/分钟时,生长增加了约一个数量级,脂肪酶产量增加了约6倍。脂肪酶的产生发生在细胞生长减速期间。产生了一种高度稳定的脂肪酶,即使在运行一个月后,它在生物反应器中仍保留其活性。使用硫酸铵沉淀技术对这种稳定的脂肪酶进行了部分纯化。分别使用300U粗脂肪酶和部分纯化的脂肪酶水解蓖麻油。部分纯化的脂肪酶在96小时内可将约81%的蓖麻油水解,而使用粗脂肪酶时,在216小时内仅获得63%的水解率。