Mernitz G, Koch A, Henrissat B, Schulz G
AG Mikrobiologie, Institut für Biologie, Humboldt-Universität zu Berlin, D-14532 Kleinmachnow, Germany.
Curr Genet. 1996 Apr;29(5):490-5. doi: 10.1007/BF02221519.
The cDNA coding for the endoglucanase EGII of P. janthinellum was cloned and sequenced. The open reading frame comprises 1230 nucleotides and the deduced amino-acid sequence shows an overall homology of 63% with the T. reesei egl2. The cellulose-binding domain of EGII represents a typical member of the A family of cellulases. The egl2 gene is only induced by cellulose or cellobiose and not by sophorose. A promotor fragment including 1 kb was cloned and sequenced. Three major transcription startpoints were identified. Five motifs matching the binding site of the carbon-catabolite repressor CREA of A. nidulans were detected. Their potential implication in repression was analyzed by bandshift assays.
克隆并测序了编码浅黄卧孔菌内切葡聚糖酶EGII的cDNA。开放阅读框由1230个核苷酸组成,推导的氨基酸序列与里氏木霉egl2的总体同源性为63%。EGII的纤维素结合结构域是纤维素酶A家族的典型成员。egl2基因仅由纤维素或纤维二糖诱导,而不由槐糖诱导。克隆并测序了一个包含1 kb的启动子片段。鉴定出三个主要转录起始点。检测到五个与构巢曲霉碳分解代谢物阻遏物CREA结合位点匹配的基序。通过凝胶迁移试验分析了它们在阻遏中的潜在作用。