Ogino Hiroyasu, Mimitsuka Takashi, Muto Toshiaki, Matsumura Miharu, Yasuda Masahiro, Ishimi Kosaku, Ishikawa Haruo
Department of Chemical Engineering, Osaka Prefecture University, Osaka, Japan.
J Mol Microbiol Biotechnol. 2004;7(4):212-23. doi: 10.1159/000079830.
A lipolytic enzyme gene (lip8) was cloned from organic solvent-tolerant Pseudomonas aeruginosa LST-03 and sequenced. In the sequenced nucleotides, an open reading frame consisting of 1,173 nucleotides and encoding 391 amino acids was found. Lip8 is considered to belong to the family VIII of lipolytic enzymes whose serine in the consensus sequence of -Ser-Xaa-Xaa-Lys- acts as catalytic nucleophile. The gene was expressed in Escherichia coli and purified by a combination of ammonium sulfate fractionation and hydrophobic interaction and ion-exchange chromatographies to homogeneity on SDS-PAGE analysis. The optimum temperature and heat stability of Lip8 were not as high as those of Lip3 and LST-03 lipase, two other lipolytic enzymes from the same strain. Addition of glycerol to a solution containing Lip8 stabilized this enzyme. By measuring the activities against various triacylglycerols and fatty acid methyl esters having carbon chains of different lengths, Lip8 was categorized as an esterase which has higher activities against fatty acid methyl esters with short-chain fatty acids.
从耐有机溶剂的铜绿假单胞菌LST - 03中克隆了一种脂解酶基因(lip8)并进行了测序。在测序的核苷酸中,发现了一个由1173个核苷酸组成、编码391个氨基酸的开放阅读框。Lip8被认为属于脂解酶家族VIII,其在 -Ser-Xaa-Xaa-Lys- 共有序列中的丝氨酸作为催化亲核试剂。该基因在大肠杆菌中表达,并通过硫酸铵分级分离、疏水相互作用和离子交换色谱法相结合进行纯化,在SDS - PAGE分析中达到均一性。Lip8的最适温度和热稳定性不如来自同一菌株的另外两种脂解酶Lip3和LST - 03脂肪酶。向含有Lip8的溶液中添加甘油可使该酶稳定。通过测量对具有不同长度碳链的各种三酰甘油和脂肪酸甲酯的活性,Lip8被归类为一种酯酶,其对短链脂肪酸的脂肪酸甲酯具有更高的活性。