ISOLATION, SEQUENCE AND OVEREXPRESSION OF THE GENE ENCODING NAD-DEPENDENT FORMATE DEHYDROGENASE FROM THE METHYLOTROPHIC YEAST CANDIDA-METHYLICA

被引:38
|
作者
ALLEN, SJ [1 ]
HOLBROOK, JJ [1 ]
机构
[1] UNIV BRISTOL,CTR MOLEC RECOGNIT,BRISTOL BS8 1TD,AVON,ENGLAND
关键词
RECOMBINANT DNA; POLYMERASE CHAIN REACTION; AMINO-ACID SEQUENCE COMPARISON;
D O I
10.1016/0378-1119(95)00347-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
NAD-dependent formate dehydrogenase (FDH) was isolated from Candida methylica (Cm) grown on 0.5% methanol. Its N-terminal amino acid (aa) sequence was determined, as was that of a commercial FDH from Candida boidinii. Degenerate oligodeoxyribonucleotides were made to the 5' region of the fdh gene from Cm using this information and to the 3' region using C-terminal aa sequence data from the methylotropic yeast, Hansenula polymorpha. An almost complete 1,1-kb fragment was amplified from Cm genomic DNA via the polymerase chain reaction (PCR). This fragment was cloned, sequenced and used to probe a Southern blot, from which a 3.4-kb EcoRI fragment containing the fdh open reading frame (ORF) was isolated. The complete nucleotide sequence of this fdh ORF was determined and corresponds to a protein of 364 aa (40 343 Da). The ORF of fdh was cloned into pKK223-3 using PCR and transformed into Escherichia coli. Enzymatically active FDH was produced to 15% of soluble E. coli protein. The deduced aa sequence of this FDH is compared to the aa sequences of four known FDH, from bacteria, yeast, fungi and plant mitochondria.
引用
收藏
页码:99 / 104
页数:6
相关论文
共 50 条
  • [31] STRUCTURAL ORGANIZATION OF THE MURINE GENE ENCODING NAD-DEPENDENT METHYLENETETRAHYDROFOLATE DEHYDROGENASE-METHENYLTETRAHYDROFOLATE CYCLOHYDROLASE
    BELANGER, C
    MACKENZIE, RE
    GENE, 1991, 97 (02) : 283 - 288
  • [32] ISOLATION AND CHARACTERIZATION OF CDNA CLONES ENCODING THE MURINE NAD-DEPENDENT METHYLENETETRAHYDROFOLATE DEHYDROGENASE-METHENYLTETRAHYDROFOLATE CYCLOHYDROLASE
    BELANGER, C
    MACKENZIE, RE
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1989, 264 (09) : 4837 - 4843
  • [33] The Isolation, Purification, and Some Properties of NAD-Dependent Isocitrate Dehydrogenase from the Organic Acid–Producing Yeast Yarrowia lipolytica
    I. G. Morgunov
    S. V. Kamzolova
    A. P. Sokolov
    T. V. Finogenova
    Microbiology, 2004, 73 : 249 - 254
  • [34] PURIFICATION AND CHARACTERIZATION OF ACTIVE AND INACTIVE NAD-DEPENDENT GLUTAMATE-DEHYDROGENASE FROM YEAST
    HEMMINGS, BA
    FEDERATION PROCEEDINGS, 1978, 37 (06) : 1810 - 1810
  • [35] Cloning of NAD-dependent sorbitol dehydrogenase from apple fruit and gene expression
    Yamada, K
    Oura, Y
    Mori, H
    Yamaki, S
    PLANT AND CELL PHYSIOLOGY, 1998, 39 (12) : 1375 - 1379
  • [36] Crystal structures of complexes of NAD+-dependent formate dehydrogenase from methylotrophic bacterium Pseudomonas sp. 101 with formate
    E. V. Filippova
    K. M. Polyakov
    T. V. Tikhonova
    T. N. Stekhanova
    K. M. Boiko
    I. G. Sadykhov
    V. I. Tishkov
    V. O. Popov
    N. Labru
    Crystallography Reports, 2006, 51 : 627 - 631
  • [37] Synthesis of Formate from CO2 Gas Catalyzed by an O2-Tolerant NAD-Dependent Formate Dehydrogenase and Glucose Dehydrogenase
    Yu, Xuejun
    Niks, Dimitri
    Ge, Xin
    Liu, Haizhou
    Hille, Russ
    Mulchandani, Ashok
    BIOCHEMISTRY, 2019, 58 (14) : 1861 - 1868
  • [38] Overexpression, purification, and biochemical characterization of the thermostable NAD-dependent alcohol dehydrogenase from Bacillus stearothermophilus
    Shim, EJ
    Jeon, SH
    Kong, KH
    JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2003, 13 (05) : 738 - 744
  • [39] INTERNAL SYMMETRY OF THE TERTIARY STRUCTURE OF NAD-DEPENDENT FORMATE DEHYDROGENASE FROM PSEUDOMONAS SP-101
    KUTSENKO, KS
    KOROLEV, SV
    LAMZIN, VS
    POPOV, VO
    MOLECULAR BIOLOGY, 1994, 28 (03) : 415 - 419
  • [40] IDENTIFICATION OF A MAJOR SOLUBLE-PROTEIN IN MITOCHONDRIA FROM NONPHOTOSYNTHETIC TISSUES AS NAD-DEPENDENT FORMATE DEHYDROGENASE
    DESFRANCSSMALL, CC
    AMBARDBRETTEVILLE, F
    SMALL, ID
    REMY, R
    PLANT PHYSIOLOGY, 1993, 102 (04) : 1171 - 1177