Effects of sublethal UVA irradiation on activity levels of oxidative defense enzymes and protein oxidation in Escherichia coli

被引:82
作者
Hoerter, JD [1 ]
Arnold, AA [1 ]
Kuczynska, DA [1 ]
Shibuya, A [1 ]
Ward, CS [1 ]
Sauer, MG [1 ]
Gizachew, A [1 ]
Hotchkiss, TM [1 ]
Fleming, TJ [1 ]
Johnson, S [1 ]
机构
[1] Ferris State Univ, Dept Biol Sci, Big Rapids, MI 49307 USA
关键词
glutathione reductase; hydroperoxidase; HPI; HPII; SOD; UVA;
D O I
10.1016/j.jphotobiol.2005.07.005
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
When bacterial cells are stressed by a change in the environment, they respond by changing the activity of enzymes at both the transcriptional and post-transcriptional levels. The UVA component (400-315 nm) of solar radiation reaching the Earth's surface is one of the most common stresses encountered by bacteria in their environment. Bacteria have evolved various antioxidant defense systems to increase survival when subjected to the deleterious effects of UVA irradiation. Recently, UVA-induced cytotoxicity and oxidative damage have been shown to be dependent on radiation intensity and dose distribution, not just total energy dose. We now report that when Escherichia coli is subjected to continuous sublethal, low-fluence UVA irradiation (7.4 W/m(2)) while growing to stationary phase, it responds by changing the activity levels of hydroperoxidases (HPI, HPII), glutathione reductase and manganese superoxide dismutase. This leads to an attenuation of the growth-delay response and an increase resistance to lethal UVA irradiation. When E. coli is given a UVA dose of 135 kJ/m(2) delivered at a fluence rate of 50 W/m(2), extensive protein oxidation occurs which may contribute to the inhibition of key cellular enzymes, leading to cellular dysfunction, DNA damage and eventually death. Changes in antioxidant enzymes induced by low-fluence UVA irradiation do not confer greater protection from protein oxidation after a challenge dose of UVA irradiation delivered at a fluence rate of 50 W/m(2). (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 180
页数:10
相关论文
共 34 条
[1]   SUPEROXIDE DISMUTASE - IMPROVED ASSAYS AND AN ASSAY APPLICABLE TO ACRYLAMIDE GELS [J].
BEAUCHAM.C ;
FRIDOVIC.I .
ANALYTICAL BIOCHEMISTRY, 1971, 44 (01) :276-&
[2]   ENDONUCLEASE-IV OF ESCHERICHIA-COLI IS INDUCED BY PARAQUAT [J].
CHAN, E ;
WEISS, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3189-3193
[3]   POSITIVE CONTROL OF A REGULON FOR DEFENSES AGAINST OXIDATIVE STRESS AND SOME HEAT-SHOCK PROTEINS IN SALMONELLA-TYPHIMURIUM [J].
CHRISTMAN, MF ;
MORGAN, RW ;
JACOBSON, FS ;
AMES, BN .
CELL, 1985, 41 (03) :753-762
[4]   EFFECTS OF MOLECULAR-OXYGEN ON DETECTION OF SUPEROXIDE RADICAL WITH NITROBLUE TETRAZOLIUM AND ON ACTIVITY STAINS FOR CATALASE [J].
CLARE, DA ;
DUONG, MN ;
DARR, D ;
ARCHIBALD, F ;
FRIDOVICH, I .
ANALYTICAL BIOCHEMISTRY, 1984, 140 (02) :532-537
[5]   ADAPTIVE RESPONSE AND OXIDATIVE STRESS [J].
CRAWFORD, DR ;
DAVIES, KJA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :25-28
[6]   Effect of growth phase on the Escherichia coli response to ultraviolet-A radiation:: influence of conditioned media, hydrogen peroxide and acetate [J].
Dantur, KI ;
Pizarro, RA .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2004, 75 (1-2) :33-39
[7]  
DAVIS NK, 1982, J GEN MICROBIOL, V128, P1631
[8]   Fur positive regulation of iron superoxide dismutase in Escherichia coli:: Functional analysis of the sodB promoter [J].
Dubrac, S ;
Touati, D .
JOURNAL OF BACTERIOLOGY, 2000, 182 (13) :3802-3808
[9]   TOXICITY AND MUTAGENICITY OF PLUMBAGIN AND THE INDUCTION OF A POSSIBLE NEW DNA-REPAIR PATHWAY IN ESCHERICHIA-COLI [J].
FARR, SB ;
NATVIG, DO ;
KOGOMA, T .
JOURNAL OF BACTERIOLOGY, 1985, 164 (03) :1309-1316
[10]   MUTAGENESIS AND GROWTH DELAY INDUCED IN ESCHERICHIA-COLI BY NEAR-ULTRAVIOLET RADIATIONS [J].
FAVRE, A ;
HAJNSDORF, E ;
THIAM, K ;
DEARAUJO, AC .
BIOCHIMIE, 1985, 67 (3-4) :335-342