Bacterial Strain Alcaligenes denitrificans C-32 Containing Two Nitrilases with Different Substrate Specificities

被引:3
作者
Novikov, A. D. [1 ]
Riabchenko, L. E. [1 ]
Leonova, T. E. [1 ]
Larikova, G. A. [1 ]
Lavrov, K. V. [1 ]
Glinskii, S. A. [1 ]
Yanenko, A. S. [1 ]
机构
[1] Res Inst Genet & Select Ind Microorganisms GosNII, Moscow 117545, Russia
基金
俄罗斯科学基金会;
关键词
Alcaligenes denitrificans; nitrilase; cloning; gene expression; substrate specificity; AMINO-ACID AMIDOHYDROLASE; CRYSTAL-STRUCTURE; ENZYMES; FAMILY;
D O I
10.1134/S0003683817080051
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Two genes encoding nitrilases with different properties have been found in an Alcaligenes denitrificans C-32 strain with high nitrilase activity that is currently used as a biocatalyst for commercial ammonium acrylate production. Both genes were expressed in E. coli, and the properties of the recombinant nitrilases were studied. One of these genes, which is designated as nitC1, controlled the formation of nitrilase that preferred aliphatic nitriles (acrylonitrile and butyronitrile) as best substrates. The nucleotide sequence of the gene nitC1 was almost (99%) identical to the gene sequence of an aliphatic nitrilase from Acidovorax facilis 72W (DQ4444267). In turn, nitC2 had a high level of homology (85%) with the arylacetonitrilase gene from Alcaligenes faecalis JM3 (D13419). Benzyl cyanide was shown to be the best substrate for nitC2-encoded nitrilase. In light of the results of DNA homology and differences in substrate specificity, the NitC2 and NitC1 nitrilases from Alcaligenes denitrificans C-32 were allocated to the groups of aliphatic nitrilases and arylacetonitrilases, respectively.
引用
收藏
页码:786 / 791
页数:6
相关论文
共 11 条
  • [1] BIRNBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513
  • [2] A NEW FAMILY OF CARBON-NITROGEN HYDROLASES
    BORK, P
    KOONIN, EV
    [J]. PROTEIN SCIENCE, 1994, 3 (08) : 1344 - 1346
  • [3] Glinskii S. A., 2010, Biotekhnologiya, P17
  • [4] A NOVEL NITRILASE, ARYLACETONITRILASE, OF ALCALIGENES-FAECALIS JM3 - PURIFICATION AND CHARACTERIZATION
    NAGASAWA, T
    MAUGER, J
    YAMADA, H
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 194 (03): : 765 - 772
  • [5] Crystal structure of N-carbamyl-D-amino acid amidohydrolase with a novel catalytic framework common to amidohydrolases
    Nakai, T
    Hasegawa, T
    Yamashita, E
    Yamamoto, M
    Kumasaka, T
    Ueki, T
    Nanba, H
    Ikenaka, Y
    Takahashi, S
    Sato, M
    Tsukihara, T
    [J]. STRUCTURE, 2000, 8 (07) : 729 - 737
  • [6] The nitrilase family of CN hydrolysing enzymes - a comparative study
    O'Reilly, C
    Turner, PD
    [J]. JOURNAL OF APPLIED MICROBIOLOGY, 2003, 95 (06) : 1161 - 1174
  • [7] Osswald S, 2012, ENZYME CATALYSIS ORG, P545, DOI [10.1002/9783527639861.ch14, DOI 10.1002/9783527639861.CH14]
  • [8] Pace HC, 2001, GENOME BIOL, V2
  • [9] Riabchenko L.E., 2005, BIOTEKHNOLOGIYA, V5, P6
  • [10] Microbial nitrilases: versatile, spiral forming, industrial enzymes
    Thuku, R. N.
    Brady, D.
    Benedik, M. J.
    Sewell, B. T.
    [J]. JOURNAL OF APPLIED MICROBIOLOGY, 2009, 106 (03) : 703 - 727