Transcription of Genes Coding for Metabolic Key Functions in Nitrosomonas europaea during Aerobic and Anaerobic Growth

被引:23
作者
Beyer, Sonja [1 ]
Gilch, Stefan [1 ]
Meyer, Ortwin [1 ]
Schmidt, Ingo [1 ]
机构
[1] Univ Bayreuth, Lehrstuhl Mikrobiol, DE-95447 Bayreuth, Germany
关键词
Nitrosomonas europaea; Transcription; adaptation; Anaerobic metabolism; Pyruvate; 2-Oxoglutarate dehydrogenase; Chemoorganotrophic metabolism; AMMONIA-OXIDIZING BACTERIA; NITRIC-OXIDE; GASEOUS NO2; NITRIFYING BACTERIA; ENERGY-SOURCE; OXIDATION; EUTROPHA; CELLS; REDUCTASE; NITRIFICATION;
D O I
10.1159/000142531
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nitrosomonas europaea can grow under conditions of chemolithoautotrophic aerobic (oxygen as oxidant) as well as anaerobic [nitrogen dioxide (NO2) as oxidant] nitrification or chemoorganotrophic anaerobic pyruvate-dependent denitrification. In this study, the adaptation of the transcription (mRNA synthesis/concentration) of N. europaea to aerobic and anaerobic growth conditions was evaluated and the transcription of genes coding for metabolic key functions was analyzed: nitrogen and energy metabolism (amoA, hao, rh1, nirK, norB, nsc, aceE, ldhA, ppc, gltA, odhA, coxA), carbon dioxide fixation (cbbL), gluconeogenesis (ppsA), cell growth (ftsZ), and oxidative stress (sodB). During aerobic ammonia oxidation the specific activities of ammonia oxidation, nitrite reduction, and the growth rates correlated with the transcription level of the corresponding genes amoA/hao, nirK/norB/nsc, and cbbL/ftsZ. In anaerobically ammonia-oxidizing cells of N. europaea, the cellular mRNA concentrations of amoA, hao, rh1, coxA, cbbL, ftsZ, and sodB were reduced compared with aerobically nitrifying cells, but the mRNA levels of nirK, norB, and nsc were significantly increased. During anaerobic pyruvate-dependent denitrification, the mRNA abundance of nirK, norB, nsc, aceE, gltA, and odhA was increased, while the concentrations of amoA, hao, rh1, coxA cbbL, ftsZ, and sodB were significantly reduced. Temperature, pH value, and NH4+, O-2, NO, and NO2 concentrations had comparatively small effects on the transcription of the studied genes. Copyright (C) 2008 S. Karger AG, Basel
引用
收藏
页码:187 / 197
页数:11
相关论文
共 53 条
[1]   ANAEROBIC METABOLISM OF NITROSOMONAS-EUROPAEA [J].
ABELIOVICH, A ;
VONSHAK, A .
ARCHIVES OF MICROBIOLOGY, 1992, 158 (04) :267-270
[2]  
AMARASINGHAM CR, 1965, J BIOL CHEM, V240, P3664
[3]   O2 AND H2O ARE EACH THE SOURCE OF ONE O IN NO2- PRODUCED FROM NH3 BY NITROSOMONAS - N-15-NMR EVIDENCE [J].
ANDERSSON, KK ;
HOOPER, AB .
FEBS LETTERS, 1983, 164 (02) :236-240
[4]   The impact of genome analyses on our understanding of ammonia-oxidizing bacteria [J].
Arp, Daniel J. ;
Chain, Patrick S. G. ;
Klotz, Martin G. .
ANNUAL REVIEW OF MICROBIOLOGY, 2007, 61 :503-528
[5]   Expression of nitrite reductase in Nitrosomonas europaea involves NsrR, a novel nitrite-sensitive transcription repressor [J].
Beaumont, HJE ;
Lens, SI ;
Reijnders, WNM ;
Westerhoff, HV ;
van Spanning, RJM .
MOLECULAR MICROBIOLOGY, 2004, 54 (01) :148-158
[6]   Novel nirK cluster genes in Nitrosomonas europaea are required for NirK-dependent tolerance to nitrite [J].
Beaumont, HJE ;
Lens, SI ;
Westerhoff, HV ;
van Spanning, RJA .
JOURNAL OF BACTERIOLOGY, 2005, 187 (19) :6849-6851
[7]   Nitrite reductase of Nitrosomonas europaea is not essential for production of gaseous nitrogen oxides and confers tolerance to nitrite [J].
Beaumont, HJE ;
Hommes, NG ;
Sayavedra-Soto, LA ;
Arp, DJ ;
Arciero, DM ;
Hooper, AB ;
Westerhoff, HV ;
van Spanning, RJM .
JOURNAL OF BACTERIOLOGY, 2002, 184 (09) :2557-+
[8]   NITROGEN LOSS CAUSED BY DENITRIFYING NITROSOMONAS CELLS USING AMMONIUM OR HYDROGEN AS ELECTRON-DONORS AND NITRITE AS ELECTRON-ACCEPTOR [J].
BOCK, E ;
SCHMIDT, I ;
STUVEN, R ;
ZART, D .
ARCHIVES OF MICROBIOLOGY, 1995, 163 (01) :16-20
[9]   The respiratory chain of Corynebacterium glutamicum [J].
Bott, M ;
Niebisch, A .
JOURNAL OF BIOTECHNOLOGY, 2003, 104 (1-3) :129-153
[10]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3