Boekema Bouke K H L, Beselin Anke, Breuer Michael, Hauer Bernhard, Koster Margot, Rosenau Frank, Jaeger Karl-Erich, Tommassen Jan
Department of Molecular Microbiology, Utrecht University, Padualaan 8, 3584 CH Utrecht, The Netherlands.
Appl Environ Microbiol. 2007 Jun;73(12):3838-44. doi: 10.1128/AEM.00097-07. Epub 2007 Apr 27.
Burkholderia glumae strain PG1 produces a lipase of biotechnological relevance. Lipase production by this strain and its derivative LU8093, which was obtained through classical strain improvement, was investigated under different conditions. When 10% hexadecane was included in the growth medium, lipolytic activity in both strains could be increased approximately 7-fold after 24 h of growth. Hexadecane also stimulated lipase production in a strain containing the lipase gene fused to the tac promoter, indicating that hexadecane did not affect lipase gene expression at the transcriptional level, which was confirmed using lipA-gfp reporter constructs. Instead, hexadecane appeared to enhance lipase secretion, since the amounts of lipase in the culture supernatant increased in the presence of hexadecane, with a concomitant decrease in the cells, even when protein synthesis was inhibited with chloramphenicol. In the presence of olive oil as a carbon source, nonionic detergents, such as Tween 80, increased extracellular lipase activity twofold. Like hexadecane, Tween 80 appeared to stimulate lipase secretion, although in a more disruptive manner, since other, normally nonsecreted proteins were found in the culture supernatant. Additionally, like olive oil, Tween 80 was found to induce lipase gene expression in strain PG1 in medium containing sucrose as a carbon source but not in glucose-containing medium, suggesting that lipase gene expression is prone to catabolite repression. In contrast, lipase production in the lipase-overproducing strain LU8093 was independent of the presence of an inducer and was not inhibited by glucose. In conclusion, hexadecane and Tween 80 enhance lipase production in B. glumae, and they act via different mechanisms.
菠萝泛菌菌株PG1可产生具有生物技术相关性的脂肪酶。研究了该菌株及其通过经典菌株改良获得的衍生物LU8093在不同条件下的脂肪酶产生情况。当生长培养基中添加10%十六烷时,两种菌株在生长24小时后的脂解活性可提高约7倍。十六烷还刺激了含有与tac启动子融合的脂肪酶基因的菌株中脂肪酶的产生,这表明十六烷在转录水平上不影响脂肪酶基因的表达,使用lipA-gfp报告构建体证实了这一点。相反,十六烷似乎增强了脂肪酶的分泌,因为在十六烷存在的情况下,培养上清液中脂肪酶的量增加,而细胞中的脂肪酶量相应减少,即使在用氯霉素抑制蛋白质合成时也是如此。以橄榄油作为碳源时,非离子洗涤剂(如吐温80)可使细胞外脂肪酶活性提高两倍。与十六烷一样,吐温80似乎也刺激了脂肪酶的分泌,尽管方式更具破坏性,因为在培养上清液中发现了其他通常不分泌的蛋白质。此外,与橄榄油一样,发现吐温80在以蔗糖作为碳源的培养基中可诱导PG1菌株中的脂肪酶基因表达,但在含葡萄糖的培养基中则不能,这表明脂肪酶基因表达易于受到分解代谢物阻遏。相比之下,脂肪酶高产菌株LU8093中脂肪酶的产生与诱导剂的存在无关,且不受葡萄糖的抑制。总之,十六烷和吐温80可提高菠萝泛菌中脂肪酶的产量,且它们通过不同的机制起作用。