Role of the Nfo (YqfS) and ExoA apurinic/apyrimidinic endonucleases in protecting Bacillus subtilis spores from DNA damage

被引:26
作者
Salas-Pacheco, JA
Setlow, B
Setlow, P
Pedraza-Reyes, M
机构
[1] Univ Guanajuato, Fac Chem, Inst Invest Expt Biol, Guanajuato 36050, Mexico
[2] Univ Connecticut, Ctr Hlth, Dept Mol Microbial & Struct Biol, Farmington, CT 06032 USA
关键词
D O I
10.1128/JB.187.21.7374-7381.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Bacillus subtilis enzymes ExoA and Nfo (originally termed YqfS) are endonucleases that can repair apurinic/apyrimidinic (A-P) sites and strand breaks in DNA. We have analyzed how the lack of ExoA and Nfo affects the resistance of growing cells and dormant spores of B. subtilis to a variety of treatments, some of which generate AP sites and DNA strand breaks. The lack of ExoA and Nfo sensitized spores (termed alpha(-)beta(-)) lacking the majority of their DNA-protective alpha/beta-type small, acid-soluble spore proteins (SASP) to wet heat. However, the lack of these enzymes had no effect on the wet-heat resistance of spores that retained alpha/beta-type SASP. The lack of either ExoA or Nfo sensitized wild-type spores to dry heat, but loss of both proteins was necessary to sensitize alpha(-)beta(-) spores to dry heat. The lack of ExoA and Nfo also sensitized alpha(-)beta(-), but not wild-type, spores to desiccation. In contrast, loss of ExoA and Nfo did not sensitize growing cells or wild-type or alpha(-)beta(-) spores to hydrogen peroxide or t-butylhydroperoxide. Loss of ExoA and Nfo also did not increase the spontaneous mutation frequency of growing cells. exoA expression took place not only in growing cells, but also in the forespore compartment of the sporulating cell. These results, together with those from previous work, suggest that ExoA and Nfo are additional factors that protect B. subtilis spores from DNA damage accumulated during spore dormancy.
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页码:7374 / 7381
页数:8
相关论文
共 40 条
[11]  
FERRARI E, 1985, MOL BIOL MICROBIAL D, P180
[12]  
FRIEDBERG EC, 1995, DNA REPAIR MUTAGENES
[13]   Antibiotic-resistance cassettes for Bacillus subtilis [J].
GueroutFleury, AM ;
Shazand, K ;
Frandsen, N ;
Stragier, P .
GENE, 1995, 167 (1-2) :335-336
[14]  
HALDENWANG WG, 1995, MICROBIOL REV, V59, P1
[15]   Compartmentalization of gene expression during Bacillus subtilis spore formation [J].
Hilbert, DW ;
Piggot, PJ .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (02) :234-+
[16]   Structure of the DNA repair enzyme endonuclease IV and its DNA complex: Double-nucleotide flipping at abasic sites and three-metal-ion catalysis [J].
Hosfield, DJ ;
Guan, Y ;
Haas, BJ ;
Cunningham, RP ;
Tainer, JA .
CELL, 1999, 98 (03) :397-408
[17]   A NEOMYCIN RESISTANCE GENE CASSETTE SELECTABLE IN A SINGLE COPY STATE IN THE BACILLUS-SUBTILIS CHROMOSOME [J].
ITAYA, M ;
KONDO, K ;
TANAKA, T .
NUCLEIC ACIDS RESEARCH, 1989, 17 (11) :4410-4410
[18]   IDENTIFICATION AND LOCATION OF L-GLYCERATE, AN UNUSUAL ACYL SUBSTITUENT IN GELLAN GUM [J].
KUO, MS ;
MORT, AJ ;
DELL, A .
CARBOHYDRATE RESEARCH, 1986, 156 :173-187
[19]   ESSENTIAL ROLE OF SMALL, ACID-SOLUBLE SPORE PROTEINS IN RESISTANCE OF BACILLUS-SUBTILIS SPORES TO UV-LIGHT [J].
MASON, JM ;
SETLOW, P .
JOURNAL OF BACTERIOLOGY, 1986, 167 (01) :174-178
[20]   REGULATION OF EXPRESSION OF GENES-CODING FOR SMALL, ACID-SOLUBLE PROTEINS OF BACILLUS-SUBTILIS SPORES - STUDIES USING LACZ GENE FUSIONS [J].
MASON, JM ;
HACKETT, RH ;
SETLOW, P .
JOURNAL OF BACTERIOLOGY, 1988, 170 (01) :239-244