Cloning, sequencing, and expression of clustered genes encoding beta-hydroxybutyryl-coenzyme A (CoA) dehydrogenase, crotonase, and butyryl-CoA dehydrogenase from Clostridium acetobutylicum ATCC 824

被引:105
作者
Boynton, ZL [1 ]
Bennett, GN [1 ]
Rudolph, FB [1 ]
机构
[1] RICE UNIV, DEPT BIOCHEM & CELL BIOL, INST BIOSCI & BIOENGN, HOUSTON, TX 77005 USA
关键词
D O I
10.1128/jb.178.11.3015-3024.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The enzymes beta-hydroxybutyryl-coenzyme A (CoA) dehydrogenase (BHBD), crotonase, and butyryl-CoA dehydrogenase (BCD) from Clostridium acetobutylicum are responsible for the formation of butyryl-CoA from acetoacetyl-CoA. These enzymes are essential to both acid formation and solvent formation by clostridia. Clustered genes encoding BHBD, crotonase, BCD, and putative electron transfer flavoprotein alpha and beta subunits have been cloned and sequenced. The nucleotide sequence of the crt gene indicates that it encodes crotonase, a protein with 261 amino acid residues and a calculated molecular mass of 28.2 kDa; the hbd gene encodes BHBD, with 282 residues and a molecular mass of 30.5 kDa. Three open reading frames (bcd, etfB, and etfA) are located between crt and hbd. The nucleotide sequence of bcd indicates that it encodes BCD, which consists of 379 amino acid residues and has high levels of homology with various acyl-CoA dehydrogenases. Open reading frames etfB and etfA, located downstream of bcd, encode 27.2- and 36.1-kDa proteins, respectively, and show homology with the fixAB genes and the alpha and beta subunits of the electron transfer flavoprotein. These findings suggest that BCD in clostridia might interact with the electron transfer flavoprotein in its redox function. Primer extension analysis identified a promoter consensus sequence upstream of the crt gene, suggesting that the clustered genes are transcribed as a transcriptional unit and form a BCS (butyryl-CoA synthesis) operon. A DNA fragment containing the entire BCS operon was subcloned into an Escherichia coli-C. acetobutylicum shuttle vector. Enzyme activity assays showed that crotonase and BHBD were highly overproduced in cell extracts from E. coli harboring the subclone. In C. acetobutylicum harboring the subclone, the activities of the enzymes crotonase, BHBD, and BCD were elevated.
引用
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页码:3015 / 3024
页数:10
相关论文
共 71 条
  • [1] NUCLEOTIDE-SEQUENCE OF THE FIXABC REGION OF AZORHIZOBIUM-CAULINODANS ORS571 - SIMILARITY OF THE FIXB PRODUCT WITH EUKARYOTIC FLAVOPROTEINS, CHARACTERIZATION OF FIXX, AND IDENTIFICATION OF NIFW
    ARIGONI, F
    KAMINSKI, PA
    HENNECKE, H
    ELMERICH, C
    [J]. MOLECULAR & GENERAL GENETICS, 1991, 225 (03): : 514 - 520
  • [2] CHARACTERIZATION OF WILD-TYPE AND AN ACTIVE-SITE MUTANT IN ESCHERICHIA-COLI OF SHORT-CHAIN ACYL-COA DEHYDROGENASE FROM MEGASPHAERA-ELSDENII
    BECKER, DF
    FUCHS, JA
    BANFIELD, DK
    FUNK, WD
    MACGILLIVRAY, RTA
    STANKOVICH, MT
    [J]. BIOCHEMISTRY, 1993, 32 (40) : 10736 - 10742
  • [3] BEDZYK LA, 1993, J BIOL CHEM, V268, P20211
  • [4] Beinert H., 1963, ENZYMES, P447
  • [5] SCREENING GAMMAGT RECOMBINANT CLONES BY HYBRIDIZATION TO SINGLE PLAQUES INSITU
    BENTON, WD
    DAVIS, RW
    [J]. SCIENCE, 1977, 196 (4286) : 180 - 182
  • [6] STRUCTURE OF L-3-HYDROXYACYL-COENZYME-A DEHYDROGENASE - PRELIMINARY CHAIN TRACING AT 2.8-A RESOLUTION
    BIRKTOFT, JJ
    HOLDEN, HM
    HAMLIN, R
    XUONG, NH
    BANASZAK, LJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) : 8262 - 8266
  • [7] AMINO-ACID-SEQUENCE OF L-3-HYDROXYACYL COA DEHYDROGENASE FROM PIG-HEART MUSCLE
    BITAR, KG
    PEREZARANDA, A
    BRADSHAW, RA
    [J]. FEBS LETTERS, 1980, 116 (02) : 196 - 198
  • [8] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [9] BROSS P, 1990, J BIOL CHEM, V265, P7116
  • [10] BULLOCK WO, 1987, BIOTECHNIQUES, V5, P376