The GacS sensor kinase regulates alginate and poly-β-hydroxybutyrate production in Azotobacter vinelandii

被引:49
作者
Castañeda, M [1 ]
Guzmán, J [1 ]
Moreno, S [1 ]
Espín, G [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Mol Microbiol, Cuernavaca 62250, Morelos, Mexico
关键词
D O I
10.1128/JB.182.9.2624-2628.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Azotobacter vinelandii produces two polymers: the extracellular polysaccharide alginate and the intracellular polyester poly-beta-hydroxybutyrate (PHB), A cosmid clone (pSMU588) from an A. vinelandii gene library diminished alginate production A.. vinelandii mucoid strain ATCC 9046. The nucleotide sequence and predicted amino acid sequence of the locus responsible for the mucoidy suppression revealed 65% identity to Pseudomonas GacS, a transmembrane sensor kinase of the two-component regulators, whose cognate response regulator, GacA, is a global activator regulating several products and virulence factors. Plasmid pMC15, harboring gacS, and a strain carrying a gacS nonpolar mutation were constructed. Either pMC15 or the gacS mutation significantly reduced alginate production and transcription of algD, the gene coding for the key enzyme GDP-mannose dehydrogenase of the alginate biosynthetic pathway. We found that the gacS mutation also reduced PHB accumulation and impaired encystment. Taken together, these data indicate that in A. vinelandii the gacSA global system regulates polymer synthesis.
引用
收藏
页码:2624 / 2628
页数:5
相关论文
共 34 条
  • [1] SPECIFIC-PURPOSE PLASMID CLONING VECTORS .2. BROAD HOST RANGE, HIGH COPY NUMBER, RSF1010-DERIVED VECTORS, AND A HOST-VECTOR SYSTEM FOR GENE CLONING IN PSEUDOMONAS
    BAGDASARIAN, M
    LURZ, R
    RUCKERT, B
    FRANKLIN, FCH
    BAGDASARIAN, MM
    FREY, J
    TIMMIS, KN
    [J]. GENE, 1981, 16 (1-3) : 237 - 247
  • [2] Characterization of the gene coding for GDP-mannose dehydrogenase (algD) from Azotobacter vinelandii
    Campos, ME
    MartinezSalazar, JM
    Lloret, L
    Moreno, S
    Nunez, C
    Espin, G
    SoberonChavez, G
    [J]. JOURNAL OF BACTERIOLOGY, 1996, 178 (07) : 1793 - 1799
  • [3] Chancey ST, 1999, APPL ENVIRON MICROB, V65, P2294
  • [4] CHRISTOPHER F, 1985, DNA CLONING, V1, P165
  • [5] A GLOBAL REGULATOR OF SECONDARY METABOLITE PRODUCTION IN PSEUDOMONAS-FLUORESCENS PF-5
    CORBELL, N
    LOPER, JE
    [J]. JOURNAL OF BACTERIOLOGY, 1995, 177 (21) : 6230 - 6236
  • [6] MINI-TN5 TRANSPOSON DERIVATIVES FOR INSERTION MUTAGENESIS, PROMOTER PROBING, AND CHROMOSOMAL INSERTION OF CLONED DNA IN GRAM-NEGATIVE EUBACTERIA
    DELORENZO, V
    HERRERO, M
    JAKUBZIK, U
    TIMMIS, KN
    [J]. JOURNAL OF BACTERIOLOGY, 1990, 172 (11) : 6568 - 6572
  • [7] INTERPOSON MUTAGENESIS OF SOIL AND WATER BACTERIA - A FAMILY OF DNA FRAGMENTS DESIGNED FOR INVITRO INSERTIONAL MUTAGENESIS OF GRAM-NEGATIVE BACTERIA
    FELLAY, R
    FREY, J
    KRISCH, H
    [J]. GENE, 1987, 52 (2-3) : 147 - 154
  • [8] FREDERICK RD, 1997, MOL PLANT MICROBE IN, V7, P455
  • [9] In vitro phosphorylation study of the arc two-component signal transduction system of Escherichia coli
    Georgellis, D
    Lynch, AS
    Lin, ECC
    [J]. JOURNAL OF BACTERIOLOGY, 1997, 179 (17) : 5429 - 5435
  • [10] THE RCSB GENE, A POSITIVE REGULATOR OF COLANIC ACID BIOSYNTHESIS IN ESCHERICHIA-COLI, IS ALSO AN ACTIVATOR OF FTSZ EXPRESSION
    GERVAIS, FG
    PHOENIX, P
    DRAPEAU, GR
    [J]. JOURNAL OF BACTERIOLOGY, 1992, 174 (12) : 3964 - 3971