Amano Marie, Mizuguchi Haruka, Sano Tadahisa, Kondo Hiroki, Shinyashiki Kengo, Inagaki Junko, Tamura Takashi, Kawaguchi Tatsuya, Kusakabe Hitoshi, Imada Katsumi, Inagaki Kenji
Department of Biofunctional Chemistry, Graduate School of Environmental and Life Science, Okayama University, Okayama 700-8530, Japan; Department of Macromolecular Science, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan; Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8558, Japan; and Enzyme Sensor Co., Ltd., Tsukuba, Ibaraki 305-0047, Japan.
J Biochem. 2015 Jun;157(6):549-59. doi: 10.1093/jb/mvv012. Epub 2015 Feb 3.
L-Lysine α-oxidase (LysOX) from Trichoderma viride is a homodimeric 112 kDa flavoenzyme that catalyzes the oxidative deamination of L-lysine to form α-keto-ε-aminocaproate. LysOX severely inhibited growth of cancer cells but showed relatively low cytotoxicity for normal cells. We have determined the cDNA nucleotide sequence encoding LysOX from T. viride. The full-length cDNA consists of 2,119 bp and encodes a possible signal peptide (Met1-Arg77) and the mature protein (Ala78-Ile617). The LysOX gene have been cloned and heterologously expressed in Streptomyces lividans TK24 with the enzyme activity up to 9.8 U/ml. The enzymatic properties of the purified recombinant LysOX, such as substrate specificity and thermal stability, are same as those of native LysOX. The crystal structure of LysOX at 1.9 Å resolution revealed that the overall structure is similar to that of snake venom L-amino acid oxidase (LAAO), and the residues involved in the interaction with the amino or carboxy group of the substrate are structurally conserved. However, the entrance and the inner surface structures of the funnel to the active site, as well as the residues involved in the substrate side-chain recognition, are distinct from LAAOs. These structural differences well explain the unique substrate specificity of LysOX.
来自绿色木霉的L-赖氨酸α-氧化酶(LysOX)是一种同型二聚体的112 kDa黄素酶,可催化L-赖氨酸的氧化脱氨反应,生成α-酮-ε-氨基己酸。LysOX能严重抑制癌细胞的生长,但对正常细胞的细胞毒性相对较低。我们已经确定了编码绿色木霉LysOX的cDNA核苷酸序列。全长cDNA由2119 bp组成,编码一个可能的信号肽(Met1-Arg77)和成熟蛋白(Ala78-Ile617)。LysOX基因已被克隆,并在变铅青链霉菌TK24中进行了异源表达,酶活性高达9.8 U/ml。纯化的重组LysOX的酶学性质,如底物特异性和热稳定性,与天然LysOX相同。LysOX在1.9 Å分辨率下的晶体结构表明,其整体结构与蛇毒L-氨基酸氧化酶(LAAO)相似,与底物氨基或羧基相互作用的残基在结构上是保守的。然而,通往活性位点的漏斗状结构的入口和内表面结构,以及参与底物侧链识别的残基,与LAAO不同。这些结构差异很好地解释了LysOX独特的底物特异性。