Margolles-Clark E, Hayes C K, Harman G E, Penttilä M
VTT Biotechnology and Food Research, Espoo, Finland.
Appl Environ Microbiol. 1996 Jun;62(6):2145-51. doi: 10.1128/aem.62.6.2145-2151.1996.
The chromosomal endochitinase gene (ThEn-42) of the mycoparasite fungus Trichoderma harzianum P1 was isolated and overexpressed in the filamentous fungus Trichoderma reesei under the promoter of the major cellulase gene cbhl1. The host strain RutC-30 did not produce any endogenous endochitinase activity. The prepro region of the T harzianum endochitinase was correctly processed in T. reesei. No differences in expression were observed when the prepro region was replaced with the CBHI signal sequence. Shake flask cultivation yielded 130 mg of active enzyme per liter, which in terms of activity represents about a 20-fold increase over the endochitinase activity produced by T. harzianum. The presence of multiple copies of the expression cassette in the transformant resulted in limitation in transcription and/or regulation factors needed for full activity of the cbh1 promoter, although this was not the major limiting factor for higher expression of endochitinase. The endochitinase was very sensitive to an acidic protease at the late stages of T. reesei cultivation. T. reesei RutC-30 appeared to be tolerant of the endochitinase and can be used as a production host for this enzyme, which has antifungal activity toward plant pathogens.
哈茨木霉P1的染色体内切几丁质酶基因(ThEn-42)被分离出来,并在主要纤维素酶基因cbhl1的启动子控制下在丝状真菌里氏木霉中过表达。宿主菌株RutC-30不产生任何内源性内切几丁质酶活性。哈茨木霉内切几丁质酶的前原区在里氏木霉中得到了正确加工。当用CBHI信号序列替换前原区时,未观察到表达差异。摇瓶培养每升产生130毫克活性酶,就活性而言,比哈茨木霉产生的内切几丁质酶活性提高了约20倍。转化体中表达盒的多个拷贝的存在导致了cbh1启动子完全活性所需的转录和/或调控因子的限制,尽管这不是内切几丁质酶高表达的主要限制因素。在里氏木霉培养后期,内切几丁质酶对酸性蛋白酶非常敏感。里氏木霉RutC-30似乎对内切几丁质酶具有耐受性,可作为该酶的生产宿主,该酶对植物病原体具有抗真菌活性。