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定点突变提高细胞色素P450 BM-3吲哚羟基化能力 被引量:4

Improving indole-hydroxylation ability of cytochrome P450 BM-3 by site-directed mutagenesis
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摘要 为进一步提高细胞色素P450BM-3(A74G/F87V/L188Q)对吲哚的羟基化能力,根据酶结构与功能的关系,以突变酶E435T为基础,在168位点引入D168L突变,获得了吲哚羟基化能力得到显著提高的突变酶D168L/E435T。突变酶对吲哚的Km为1.72 mol·L-1(父本2.09 mol·L-1),转化数(kcat)为28.15min-1(父本4.04min-1),表明D168L定点突变可以略微提高酶对底物的亲和力,但主要的效应是促进了底物的转化速率,这两个效应的综合表现是使酶的催化效率(kcatKm-1)比父本酶提高了8.48倍。此外,产物中副产物靛玉红的比例也降低为1.2%(父本7.3%),这说明该突变酶催化吲哚的区域选择性上也更有利于靛蓝的生成。 According to the relationship between the structure and function of enzyme,it was speculated that the combination of the mutant enzyme D168L and E435T might improve the catalytic ability of indole to generate indigo.The mutant enzyme D168L/E435T was produced by site-directed mutagenesis conducted on the 168th site of the P450 BM-3(A74G/F87V/L188Q/E435T)and it was identified with higher hydroxylation activity toward indole in comparison to its parent enzyme.Concomitantly,its Km for indole was 1.72 mmol·L-1 and this value was lower compared to its parent enzyme(2.09 mmol·L-1).Also with the kcat=28.15 min-1,the turnover rate of the mutant enzyme was increasing up to 6.97-fold that of its parent enzyme(4.04 min-1).The catalytic efficiency(kcatKm-1)was correspondingly raised to 8.48 times as much as that of its parent enzyme.Moreover,the proportion of the byproducts indirubin reduced to 1.2%,much lower than that of its parent mutant(7.3%),which indicated that this regioselectivity of mutant enzyme to catalyze indole was more conducive to generating indigo.
出处 《化工学报》 EI CAS CSCD 北大核心 2013年第9期3331-3337,共7页 CIESC Journal
基金 国家自然科学基金项目(21176220 31240054) 浙江省自然科学基金重点项目(Z12B060008) 宁波市重大科技项目(2011C11023)~~
关键词 细胞色素P450 BM-3 定点突变 羟基化 吲哚 靛蓝 P450 BM-3 site-directed mutagenesis hydroxylation indole indigo
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  • 1吴祺.拜耳与合成靛蓝[J].化学通报,2001,64(8):527-529. 被引量:12
  • 2韩晓红,王伟,肖兴国.靛蓝及其同类色素的微生物生产与转化[J].生物工程学报,2008,24(6):921-926. 被引量:22
  • 3贾秀玲,崔运花,韩雅岚,冉唯,吴秋蒙,何旭,陆佳欢.植物靛蓝染料的开发应用现状及展望[J].纺织科技进展,2011(2):24-26. 被引量:12
  • 4马桥,曲媛媛,张旭旺,许炳雯,周集体.靛蓝的微生物合成研究新进展[J].应用与环境生物学报,2012,18(2):344-350. 被引量:27
  • 5Rosie N N. Versatile capacity of shuffled cytochrome P450s for dye production [ J ]. Appl. Microbiol. Biotechnol. , 2009, 82 (2): 203-210.
  • 6Zhang Z G, Liu Y, Guengerich F P. Identification of amino acid residues involved in 4-ehloroindole 3 hydroxylation by eytochrome P4S0 2A6 using screening of random libraries [J]. J. Biotechnol., 2009, 139 (1): 12-18.
  • 7Rosic N N, Huang W L, Johnston W A, DeVoss J J, Gillam E M J. Extending the diversity of cytochrome P450 enzymes by DNA family shuffling [J]. Gene, 2007, 39'J (1/2) 40-48.
  • 8GillamEMJ, AguinaldoAMA, NotleyLM, KimDH, Mundkowski R G, Volkov A A, Arnold F H, Soueek P, DeVoss J J, Guengerich F P. Formation of indigo by recombinant mammalian cytochrome P450 [J]. Biochem. Biophys. Res. Commun., 1999, 265 (2): 469 472.
  • 9Li Q S, Schwaneberg U, Fischer P, Schmid R D. Directed evolution of the fatty-acid hydroxylase P450 BM3 into an indole hydroxylating catalyst[J]. Chem. Eur. J. , 2000, 6 (9): 1531-1536.
  • 10van Vugt-Lussenburg B M A, Stjernschantz E, Lastdrager J, Oostenbrink C, Vermeulen N P E, Commandeur J N M. Identification of critical residues in novel drugmetabolizing mutants of cytochrome P450 BM3 using random mutagenesis [J]. J. Med. Chem. , 2007, 50 (3) : 455-461.

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  • 1高愿军,郝莉花,张鑫,南海娟,郝亚勤.猕猴桃汁维生素C降解动力学的研究[J].农业工程学报,2006,22(5):157-160. 被引量:29
  • 2董娟娥,梁宗锁,尉芹,陈胜龙.不同区域松蓝根、叶(板蓝根、大青叶)有效成分含量差异[J].应用生态学报,2006,17(9):1613-1618. 被引量:27
  • 3Singh B, Saxena A K, Chandan B K, Bhardwaj V,Gupta V N, Suri OP, Handa S S. Hepatoprotective activity of indigtone—a bioactivefraction from Indigofera tinctoria Linn[J]. Phytotherapy Research,2001,15(4): 294-297.
  • 4Hein M,Phuong N T B, Michalik D, Gorls H, Lalk M, Langer P.Synthesis of the first deprotected indigo A-glycosides (blue sugars)by reductive glycosylation of dehydroindigo[J]. Tetrahedron Lett”2006,47(32):5741-5745.
  • 5Wolf L. Blue jeans [J]. Chem. Eng. News, 2011, 89(43): 44.
  • 6Meksi N,Ben Ticha M, Kechida M, Mhenni M F. Using ofecofriendly a-hydroxycarbonyls as reducing agents to replace sodiumdithionite in indigo dyeing processes [J]. J. Clean. Prod., 2012, 24(3):149-158.
  • 7Li Q S, Schwaneberg U, Fischer P, Schmid R D. Directed evolutionof the fatty-acid hydroxylase P450 BM-3 into an indole-hydroxylatingcatalyst [J]. Chem. Eur. X,2000, 6(9): 1531-1536.
  • 8Li H M, Mei L H, Urlacher V B, Schmid R D. Cytochrome P450BM-3 evolved by random and saturation mutagenesis as an effectiveindole-hydroxylating catalyst [J]. Appl. Biochem. Biotechnol.,2008,144(1): 27-36.
  • 9Zhang P P, Hu S, Mei L H,Lei Y L,Jin Z H, Hu G X. Improving theactivity of cytochrome P450 BM-3 catalyzing indole hydroxylationby directed evolution [J]. Appl. Biochem. Biotechnoi, 2013, 171(1):93-103.
  • 10Maurer S C,Schulze H, Schmid R D, Urlacher V. Immobilisation ofP450 BM-3 and an NADP+ cofactor recycling system: towards atechnical application of heme-containing monooxygenases in finechemical synthesis [J]. Adv. Synth. Catal, 2003,345(67): 802-810.

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