Kugimiya W, Otani Y, Kohno M, Hashimoto Y
Central Research Institute, Fuji Oil Co., Ltd., Ibaraki, Japan.
Biosci Biotechnol Biochem. 1992 May;56(5):716-9. doi: 10.1271/bbb.56.716.
Complementary DNA encoding Rhizopus niveus lipase (RNL) was isolated from the R. niveus IF04759 cDNA library using a synthetic oligonucleotide corresponding to the amino acid sequence of the enzyme. A clone, which had an insert of 1.0 kilobase pairs, was found to contain the coding region of the enzyme. The lipase gene was expressed in Escherichia coli as a lacZ fusion protein. The mature RNL consisted of 297 amino acid residues with a molecular mass of 32 kDa. The RNL sequence showed significant overall homology to Rhizomucor miehei lipase and the putative active site residues were strictly conserved.
使用与该酶氨基酸序列对应的合成寡核苷酸,从米根霉IFO4759 cDNA文库中分离出编码米根霉脂肪酶(RNL)的互补DNA。发现一个插入片段为1.0千碱基对的克隆含有该酶的编码区。脂肪酶基因在大肠杆菌中作为lacZ融合蛋白表达。成熟的RNL由297个氨基酸残基组成,分子量为32 kDa。RNL序列与米黑根毛霉脂肪酶具有显著的整体同源性,且推定的活性位点残基严格保守。