Visual modeling mutants for D-lactate dehydrogenase form aquifex aeolicus and the effect of mutants on the production of phenyl lactate acid in E.coli[J]. Science and Technology of Food Industry, 2012, (19): 173-176. DOI: 10.13386/j.issn1002-0306.2012.19.055
Citation: Visual modeling mutants for D-lactate dehydrogenase form aquifex aeolicus and the effect of mutants on the production of phenyl lactate acid in E.coli[J]. Science and Technology of Food Industry, 2012, (19): 173-176. DOI: 10.13386/j.issn1002-0306.2012.19.055

Visual modeling mutants for D-lactate dehydrogenase form aquifex aeolicus and the effect of mutants on the production of phenyl lactate acid in E.coli

More Information
  • Received Date: February 16, 2012
  • Based on bioinformatics, the amino acid residues of conservative and activity center of D-lactate dehydrogenase (D-LDH) , and the three-dimensional structure model of protein was analysised.The space conformation of visualization mutant had been constructed by homology modeling, the best mutant models were selected by the calculation of the distance and angle.The results showed that the 4 amino acid residues were relevant to the activity center in 20 conservative residues of D-LDH.After the models were compared, it was found that the big molecules substrates were obstructed by the benzyl of the residues of Phenylalanine (phe) or Tyrosine (try) on the 49 and 297 position.When F49A, Y279A, F49A and Y279A were mutated, the obstacles would disappear or weaken.The three mutants constructed were made a preliminary study, the results showed that IPTG or lactose could induce mutant to produce phenyl lactic acid in E.coli.The yield of phenyl lactic acid was higher in static culture than in vibration incubator, and the one of the F49A mutant (A.a.D-LDH-F49A strains) was higher than the one of the wild type (A.a.D-LDH strains) with lactose inducing.It would be a method of constructing gene engineering strain that visualization mutants models were compared and selected.
  • loading
  • [1]
    Hummel W, Schiitte H, Kula MR.Large scale production of D-lactate dehydrogenase for the stereospecific reduction of pyruvate and phenylpyruvate[J].Europen Journal of Applied Microbiology and Biotechnology, 1983, 18:75-85.
    [2]
    Dunn CR, Wilks HM, Halsall DJ, et al.Design and synthesis of new enzymes based on the lactate dehydrogenase framework[J].Philos Trans R Soc Lond B Biol Sci, 1991, 332 (1263) :177-184.
    [3]
    El Hawrani AS, Sessions RB, Moreton KM, et al.Guided evolution of enzymes with new substrate specificities[J].Mol Biol, 1996, 264 (1) :97-110.
    [4]
    Wilks HM, Moreton KM, Halsall DJ, et al.Design of a specific phenyllactate dehydrogenase by peptide loop exchange on the Bacillus stearothermophilus lactate dehydrogenase framework[J].Biochemistry, 1992, 34:7802-7806.
    [5]
    Daff S, Manson F D, Reid G A, et al.Strategic manipulation of the substrate specificity of Saccharomyces cerevisiae flavocytochrome b2[J].Biochem J, 1994, 301:829-834.
    [6]
    Sinclair R, Reid G A, Chapman S K.Re-design of Saccharomyces cerevisiae flavocytochrome b2:introduction of L-mandelate dehydrogenase activity[J].Biochem J, 1998, 333:117-120.
    [7]
    Mowat CG, Wehenkel A, Green AJ, et al.Altered substrate specificity in flavocytoch-rome b2:structural insights into the mechanism of L-lactate dehydrogenation[J].Biochemistry, 2004, (29) :9519-9526.
    [8]
    Antonyuk S V, Strange R W, Ellis M J, et al.Structure of D-lactate dehydrogenase from Aquifex aeolicus complexed with NAD+and lactic acid (or pyruvate) [J].Acta Crystallogr Sect F Struct Biol Cryst Commun, 2009, 65 (12) :1209-1213.
    [9]
    Nielsen M, Lundegaard C, Lund O, et al.CPHmodels-3.0-Remote homology modeling using structure guided sequence profiles[J].Nucleic Acids Research, 2010, 38:10.1093/nar/gkq535.
    [10]
    O Lund, M Nielsen, C Lundegaard, et al.CPH models2.0:X3M a computer program to extract3D models[C].Abstract at the CASP5conferenceA102, 2002.
    [11]
    Arnold K, Bordoli L, Kopp J, et al.The SWISS-MODEL Workspace:A web-based environment for protein structure homology modeling[J].Bioinformatics, 2006, 22:195-201.
    [12]
    Schwede T, Kopp J, Guex N, et al.SWISS-MODEL:an automated protein homology-modeling server[J].Nucleic Acids Research, 2003, 31:3381-3385.
    [13]
    Guex N, Peitsch M C.SWISS-MODEL and the Swiss-PdbViewer:An environment for comparative protein modeling[J].Electrophoresis, 1997, 18:2714-2723.
    [14]
    贾江花, 沐万孟, 张涛, 等.重组L-乳酸脱氢酶在大肠杆菌中的表达、纯化及活性研究[J].食品与发酵工业, 2009, 35 (5) :116-119.
    [15]
    李兴峰, 江波, 潘蓓蕾, 等.苯丙氨酸及苯丙酮酸对lactobacillus sp.SK007合成苯乳酸的影响[J].过程工程学报, 2007, 7 (6) :1202-1206.
    [16]
    沐万孟, 周宏敏, 刘凤丽, 等.苯乳酸的快速检测研究[J].食品与发酵工业, 2008, 34 (11) :139-142.
    [17]
    Razeto A, Kochhar S, Hottinger H, et al.Domain closure, substrate specificity and catalysis of d-lactate dehydrogenase from lactobacillus bulgaricus[J].Journal of Molecular Biology, 2002, 318:109-119.
    [18]
    Stoll VS, Kimber MS, Pai EF.Insights into substrate binding by D-2-ketoacid dehydrogenases from the structure of Lactobacillus pentosus D-lactate dehydrogenase[J].Structure, 1996, 4:437-447.

Catalog

    Article Metrics

    Article views (103) PDF downloads (120) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return