Are UV-induced nonculturable Escherichia coli K-12 cells alive or dead?

被引:29
作者
Villarino, A
Rager, MN
Grimont, PAD
Bouvet, OMM
机构
[1] Inst Pasteur, Aquabiolab, Paris, France
[2] Inst Pasteur, INSERM, U389, Unite Biodivers Bacteries Pathogenes Emergentes, F-75724 Paris, France
[3] Ecole Natl Super Chim Paris, Serv Resonance Magnet Nucl UMR 7576, Paris, France
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2003年 / 270卷 / 12期
关键词
NMR; radiation injury; viability; metabolism; Escherichia coli;
D O I
10.1046/j.1432-1033.2003.03652.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
Cells that have lost the ability to grow in culture could be defined operationally as either alive or dead depending on the method used to determine cell viability. As a consequence, the interpretation of the state of 'nonculturable' cells is often ambiguous. Escherichia coli K12 cells inactivated by UV-irradiation with a low (UV1) and a high (UV2) dose were used as a model of nonculturable cells. Cells inactivated by the UV1 dose lost 'culturability' but they were not lysed and maintained the capacity to respond to nutrient addition by protein synthesis and cell wall synthesis. The cells also retained both a high level of glucose transport and the capacity for metabolizing glucose. Moreover, during glucose incorporation, UV1-treated cells showed the capacity to respond to aeration conditions modifying their metabolic flux through the Embden-Meyerhof and pentose-phosphate pathways. However, nonculturable cells obtained by irradiation with the high UV2 dose showed several levels of metabolic imbalance and retained only residual metabolic activities. Nonculturable cells obtained by irradiation with UV1 and UV2 doses were diagnosed as active and inactive (dying) cells, respectively.
引用
收藏
页码:2689 / 2695
页数:7
相关论文
共 33 条
[1]   COMBINATION OF 16S RIBOSOMAL-RNA-TARGETED OLIGONUCLEOTIDE PROBES WITH FLOW-CYTOMETRY FOR ANALYZING MIXED MICROBIAL-POPULATIONS [J].
AMANN, RI ;
BINDER, BJ ;
OLSON, RJ ;
CHISHOLM, SW ;
DEVEREUX, R ;
STAHL, DA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (06) :1919-1925
[2]  
APPLEYARD RK, 1954, GENETICS, V39, P440
[3]  
Bouvet OMM, 2000, NMR IN MICROBIOLOGY: THEORY AND APPLICATIONS, P349
[4]  
BRUCH CW, 1971, HUSAS PHARM DISPENSI, P592
[5]  
Caro A, 1999, APPL ENVIRON MICROB, V65, P3229
[6]   Relation between presence absence of a visible nucleoid and metabolic activity in bacterioplankton cells [J].
Choi, JW ;
Sherr, EB ;
Sherr, BF .
LIMNOLOGY AND OCEANOGRAPHY, 1996, 41 (06) :1161-1168
[7]   Flow cytometry and cell sorting of heterogeneous microbial populations: The importance of single-cell analyses [J].
Davey, HM ;
Kell, DB .
MICROBIOLOGICAL REVIEWS, 1996, 60 (04) :641-+
[8]   Metabolic flux profiling of Escherichia coli mutants in central carbon metabolism using GC-MS [J].
Fischer, E ;
Sauer, U .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (05) :880-891
[9]   Homeostatic regulation of intracellular hydrogen peroxide concentration in aerobically growing Escherichia coli [J].
GonzalezFlecha, B ;
Demple, B .
JOURNAL OF BACTERIOLOGY, 1997, 179 (02) :382-388
[10]  
Gottschalk G., 1985, BACTERIAL METABOLISM, V2nd