Lee J, Oh J, Min K R, Kim C K, Min K H, Lee K S, Kim Y C, Lim J Y, Kim Y
College of Pharmacy, Chungbuk National University, Cheongju, Korea.
Biochem Biophys Res Commun. 1996 Jul 25;224(3):831-6. doi: 10.1006/bbrc.1996.1108.
A catechol 2,3-dioxygenase gene in chromosomal DNA of P. putida KF715 was cloned and its nucleotide sequence analyzed. The enzyme gene was composed of 924 base pairs with ATG initiation codon and TGA termination codon, which can encode a polypeptide of molecular weight 35 kDa containing 307 amino acids. A promoter-like sequence and a ribosome-binding sequence were identified upstream the enzyme gene. A deduced amino acid sequence of the catechol 2,3-dioxygenase exhibited 94% identity with that of corresponding enzyme in TOL plasmid and 25% identity with that of 2,3-dihydroxybiphenyl 1,2-dioxygenase from the same strain. Furthermore, sequence comparison of the catechol 2,3-dioxygenase with other extradiol-type dioxygenases has led to identify evolutionally conserved amino acid residues whose possible catalytic roles are proposed.
克隆了恶臭假单胞菌KF715染色体DNA中的儿茶酚2,3-双加氧酶基因,并对其核苷酸序列进行了分析。该酶基因由924个碱基对组成,具有ATG起始密码子和TGA终止密码子,可编码一个分子量为35 kDa、含有307个氨基酸的多肽。在该酶基因上游鉴定出一个类似启动子的序列和一个核糖体结合序列。推导的儿茶酚2,3-双加氧酶氨基酸序列与TOL质粒中相应酶的氨基酸序列具有94%的同一性,与同一菌株的2,3-二羟基联苯1,2-双加氧酶具有25%的同一性。此外,通过将儿茶酚2,3-双加氧酶与其他间位二醇型双加氧酶进行序列比较,已鉴定出进化上保守的氨基酸残基,并对其可能的催化作用进行了推测。