CLONING AND NUCLEOTIDE-SEQUENCE OF THE PSRA GENE OF WOLINELLA-SUCCINOGENES POLYSULFIDE REDUCTASE

被引:92
作者
KRAFFT, T
BOKRANZ, M
KLIMMEK, O
SCHRODER, I
FAHRENHOLZ, F
KOJRO, E
KROGER, A
机构
[1] JW GOETHE UNIV, INST MIKROBIOL, HAUS 75A, THEODOR STERN KAI 7, W-6000 FRANKFURT, GERMANY
[2] MAX PLANCK INST BIOPHYS, W-6000 FRANKFURT 70, GERMANY
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1992年 / 206卷 / 02期
关键词
D O I
10.1111/j.1432-1033.1992.tb16953.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The polysulphide reductase (formerly sulphur reductase) of Wolinella succinogenes is a component of the phosphorylative electron transport system with polysulphide as the terminal acceptor. Using an antiserum raised against the major subunit (PsrA, 85 kDa) of the enzyme, the corresponding gene (psrA) was cloned from a lambda-gene bank. The N-terminal amino acid sequence of PsrA mapped within the psrA gene product, which also contained an apparent signal peptide. Downstream of the psrA gene two more open reading frames (psrB and psrC) were found. The three genes may form a transcriptional unit with the transcription start site in front of psrA. The three genes were present only once on the genome. PsrA is a hydrophilic protein homologous to the largest subunits of six prokaryotic molybdoenzymes. PsrB is predicted to be hydrophilic, to contain ferredoxin-like cysteine clusters and to be homologous to the smaller hydrophilic subunits of four molybdoenzymes. PsrC is predicted to be a hydrophobic protein that could possibly serve as the membrane anchor of the enzyme.
引用
收藏
页码:503 / 510
页数:8
相关论文
共 47 条
[11]   LAMBDA-REPLACEMENT VECTORS CARRYING POLYLINKER SEQUENCES [J].
FRISCHAUF, AM ;
LEHRACH, H ;
POUSTKA, A ;
MURRAY, N .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 170 (04) :827-842
[12]  
HAWKES R, 1982, ANAL BIOCHEM, V119, P142, DOI 10.1016/0003-2697(82)90677-7
[13]  
HOLTKE HJ, 1990, BIOL CHEM H-S, V371, P929
[14]   MOLYBDOPTERIN GUANINE DINUCLEOTIDE - A MODIFIED FORM OF MOLYBDOPTERIN IDENTIFIED IN THE MOLYBDENUM COFACTOR OF DIMETHYL-SULFOXIDE REDUCTASE FROM RHODOBACTER-SPHAEROIDES FORMA-SPECIALIS-DENITRIFICANS [J].
JOHNSON, JL ;
BASTIAN, NR ;
RAJAGOPALAN, KV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) :3190-3194
[15]   PHYSICAL CHARACTERIZATION OF THE RAC PROPHAGE IN ESCHERICHIA-COLI-K12 [J].
KAISER, K ;
MURRAY, NE .
MOLECULAR AND GENERAL GENETICS, 1979, 175 (02) :159-174
[16]   NOVEL BACTERIOPHAGE-LAMBDA CLONING VECTOR [J].
KARN, J ;
BRENNER, S ;
BARNETT, L ;
CESARENI, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09) :5172-5176
[17]   NONRADIOACTIVE LABELING AND DETECTION OF NUCLEIC-ACIDS .1. A NOVEL DNA LABELING AND DETECTION SYSTEM BASED ON DIGOXIGENIN - ANTI-DIGOXIGENIN ELISA PRINCIPLE (DIGOXIGENIN SYSTEM) [J].
KESSLER, C ;
HOLTKE, HJ ;
SEIBL, R ;
BURG, J ;
MUHLEGGER, K .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1990, 371 (10) :917-927
[18]   GROWTH OF WOLINELLA-SUCCINOGENES WITH POLYSULFIDE AS TERMINAL ACCEPTOR OF PHOSPHORYLATIVE ELECTRON-TRANSPORT [J].
KLIMMEK, O ;
KROGER, A ;
STEUDEL, R ;
HOLDT, G .
ARCHIVES OF MICROBIOLOGY, 1991, 155 (02) :177-182
[19]   WOLINELLA-SUCCINOGENES FUMARATE REDUCTASE CONTAINS A DIHEME CYTOCHROME-B [J].
KORTNER, C ;
LAUTERBACH, F ;
TRIPIER, D ;
UNDEN, G ;
KROGER, A .
MOLECULAR MICROBIOLOGY, 1990, 4 (05) :855-860
[20]   ORIENTATION OF THE SUBSTRATE SITES OF FORMATE DEHYDROGENASE AND FUMARATE REDUCTASE IN THE MEMBRANE OF VIBRIO-SUCCINOGENES [J].
KROGER, A ;
DORRER, E ;
WINKLER, E .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 589 (01) :118-136