Proteus mirabilis glutathione S-transferase B1-1 is involved in protective mechanisms against oxidative and chemical stresses

被引:42
作者
Allocati, N
Favaloro, B
Masulli, M
Alexeyev, MF
Di Ilio, C
机构
[1] Univ G DAnnunzio, Dipartimento Sci Biomed, I-66013 Chieti, Italy
[2] Ist Ric Farmacol Mario Negri, Consorzio Mario Negri Sud, G Paone Environm Hlth Ctr, I-66030 Santa Maria Imbaro, Italy
[3] Univ S Alabama, Dept Pharmacol, Mobile, AL 36688 USA
关键词
antimicrobial agent; bacterial glutathione S-transferase; knock-out gene; Proteus mirabilis glutathione S-transferase; stress factor; suicide vector;
D O I
10.1042/BJ20030184
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
We investigated the effects of several xenobiotics, including antimicrobial agents and general stress factors such as starvation, heat and osmotic shock, on the modulation of expression of Proteus mirabilis glutathione S-transferase B1-1 (PmGST B1-1). The level of expression of PmGST B1-1 was established by both Western- and Northern-blot experiments. Our results show that several compounds can modulate expression of PmGST B1-1. The level of PmGST B1-1 increased when bacterial cells were exposed to a variety of stresses such as 1-chloro-2,4-dinitrobenzene, H2O2, fosfomycin or tetracycline. A knock-out gstB gene was also constructed using the suicide vector pKNOCK1ox-Ap. Successful inactivation of the wild-type gene was confirmed by PCR, DNA sequence analysis and Western blotting. Under normal culture conditions, this mutant was viable and displayed no significant phenotypic differences compared with the wildtype. However, viability tests revealed that the null mutant was more sensitive to oxidative stress in the form of H2O2 and to several antimicrobial drugs when compared with the wild-type. These results suggest that PmGST B1-1 has an active role in the protection against oxidative stress generated by H2O2 and it appears to be involved in the detoxification of antimicrobial agents.
引用
收藏
页码:305 / 311
页数:7
相关论文
共 37 条
  • [1] The pKNOCK series of broad-host-range mobilizable suicide vectors for gene knockout and targeted DNA insertion into the chromosome of Gram-negative bacteria
    Alexeyev, MF
    [J]. BIOTECHNIQUES, 1999, 26 (05) : 824 - +
  • [2] Functional analysis of the evolutionarily conserved proline 53 residue in Proteus mirabilis glutathione transferase B1-1
    Allocati, N
    Casalone, E
    Masulli, M
    Ceccarelli, I
    Carletti, E
    Parker, MW
    Di Ilio, C
    [J]. FEBS LETTERS, 1999, 445 (2-3) : 347 - 350
  • [3] Evaluation of the role of two conserved active-site residues in Beta class glutathione S-transferases
    Allocati, N
    Casalone, E
    Masulli, M
    Polekhina, G
    Rossjohn, J
    Parker, MW
    Di Ilio, C
    [J]. BIOCHEMICAL JOURNAL, 2000, 351 : 341 - 346
  • [4] Glutamic acid-65 is an essential residue for catalysis in Proteus mirabilis glutathione S-transferase B1-1
    Allocati, N
    Masulli, M
    Casalone, E
    Santucci, S
    Favaloro, B
    Parker, MW
    Di Ilio, C
    [J]. BIOCHEMICAL JOURNAL, 2002, 363 (01) : 189 - 193
  • [5] IMMUNOGOLD LOCALIZATION OF GLUTATHIONE TRANSFERASE B1-1 IN PROTEUS-MIRABILIS
    ALLOCATI, N
    CELLINI, L
    ACETO, A
    IEZZI, T
    ANGELUCCI, S
    ROBUFFO, I
    DIILIO, C
    [J]. FEBS LETTERS, 1994, 354 (02): : 191 - 194
  • [6] Allocati N, 2001, CHEM-BIOL INTERACT, V133, P261
  • [7] [Anonymous], 1983, COLD SPRING HARBOR L
  • [8] Structure, catalytic mechanism, and evolution of the glutathione transferases
    Armstrong, RN
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (01) : 2 - 18
  • [9] TRANSPOSON MUTAGENESIS IN PROTEUS-MIRABILIS
    BELAS, R
    ERSKINE, D
    FLAHERTY, D
    [J]. JOURNAL OF BACTERIOLOGY, 1991, 173 (19) : 6289 - 6293
  • [10] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3