Chung G H, Lee Y P, Jeohn G H, Yoo O J, Rhee J S
Department of Biological Science and Engineering, Korea Advanced Institute of Science and Technology, Chongyang, Seoul.
Agric Biol Chem. 1991 Sep;55(9):2359-65.
A gene coding for a thermostable lipase of Pseudomonas fluorescens SIK W1 was cloned into Escherichia coli JM83 by inserting Sau3AI-generated DNA fragments into the BamHI site of pUC19. Twenty colonies with esterase activity on the tributyrin agar plate were isolated by screening the constructed Pseudomonas fluorescens genomic library. Only one out of the esterase positive 20 colonies had lipase activity on the agar plate containing olive oil and Rhodamine-B. The complete nucleotide sequence of the lipase gene was identified. The lipase gene consists of an open reading frame, 1347bp long, commencing with an ATG start codon encoding a polypeptide of 449 amino acid residues and a TGA stop codon. Comparison of this lipase amino acid sequence with those from another organisms sequenced to data showed the presence of the short homologous region Gly-X-Ser-X-Gly.
通过将Sau3AI酶切产生的DNA片段插入pUC19的BamHI位点,把编码荧光假单胞菌SIK W1耐热脂肪酶的基因克隆到大肠杆菌JM83中。通过筛选构建的荧光假单胞菌基因组文库,在三丁酸甘油酯琼脂平板上分离出20个具有酯酶活性的菌落。在含有橄榄油和罗丹明B的琼脂平板上,20个酯酶阳性菌落中只有1个具有脂肪酶活性。确定了脂肪酶基因的完整核苷酸序列。该脂肪酶基因由一个1347bp长的开放阅读框组成,起始于一个ATG起始密码子,编码一个由449个氨基酸残基组成的多肽,并以一个TGA终止密码子结束。将该脂肪酶氨基酸序列与其他已测序生物的序列进行比较,发现存在短同源区域Gly-X-Ser-X-Gly。