Physiological state, growth mode, and oxidative stress play a role in Cd(II)-mediated inhibition of Nitrosomonas europaea 19718

被引:51
作者
Chandran, Kartik [1 ]
Love, Nancy G. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Civil & Environm Engn, Blacksburg, VA 24061 USA
关键词
D O I
10.1128/AEM.01940-07
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
The goal of this study was to determine the impact of physiological growth states (batch exponential and batch stationary growth) and growth modes (substrate-limited chemostat, substrate-sufficient exponential batch, and substrate-depleted stationary batch growth) on several measures of growth and responses to Cd(II)-mediated inhibition of Nitrosomonas europaea strain 19718. The specific oxygen uptake rate (sOUR) was the most sensitive indicator of inhibition among the different responses analyzed, including total cell abundance, membrane integrity, intracellular 16S rRNA/DNA ratio, and amoA expression. This observation remained true irrespective of the physiological state, the growth mode, or the mode of Cd(II) exposure. Based on the sOUR, a strong time-dependent exacerbation of inhibition (in terms of an inhibition coefficient [K-i]) in exponential batch cultures was observed. Long-term inhibition levels (based on K-i estimates) in metabolically active chemostat and exponential batch cultures were also especially severe and comparable. In contrast, the inhibition level in stationary-phase cultures was 10-fold lower and invariable with exposure time. Different strategies for surviving substrate limitation (a 10-fold increase in amoA expression) and starvation (the retention of 16S rRNA levels) in N. europaea cultures were observed. amoA expression was most negatively impacted by Cd(II) exposure in the chemostat cultures, was less impacted in exponential batch cultures, and was least impacted in stationary batch cultures. Although the amoA response was consistent with that of the sOUR, the amoA response was not as strong. The intracellular 16S rRNA/DNA ratio, as determined by fluorescence in situ hybridization, also did not uniformly correlate with the sOUR under conditions of inhibition or no inhibition. Finally, Cd(II)-mediated inhibition of N. europaea was attributed partially to oxidative stress.
引用
收藏
页码:2447 / 2453
页数:7
相关论文
共 52 条
[1]  
[Anonymous], 2005, APHA STANDARD METHOD
[2]   An Escherichia coli gene responsive to heavy metals [J].
Babai, R ;
Ron, EZ .
FEMS MICROBIOLOGY LETTERS, 1998, 167 (02) :107-111
[3]  
BEDARD C, 1989, MICROBIOL REV, V53, P68
[4]  
BEG SA, 1982, J WATER POLLUT CON F, V54, P482
[5]   INHIBITION OF NITRIFICATION BY HEAVY-METAL CATIONS [J].
BENMOUSSA, H ;
MARTIN, G ;
RICHARD, Y ;
LEPRINCE, A .
WATER RESEARCH, 1986, 20 (11) :1333-1339
[6]   Influence of starvation on potential ammonia-oxidizing activity and amoA mRNA levels of Nitrosospira briensis [J].
Bollmann, A ;
Schmidt, I ;
Saunders, AM ;
Nicolaisen, MH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (03) :1276-1282
[7]   EFFECT OF COPPER ON NITRIFICATION IN ACTIVATED-SLUDGE [J].
BRAAM, F ;
KLAPWIJK, A .
WATER RESEARCH, 1981, 15 (09) :1093-1098
[8]   Modelling carbon responses of tundra ecosystems to historical and projected climate: sensitivity of pan-Arctic carbon storage to temporal and spatial variation in climate [J].
McGuire, AD ;
Clein, JS ;
Melillo, JM ;
Kicklighter, DW ;
Meier, RA ;
Vorosmarty, CJ ;
Serreze, MC .
GLOBAL CHANGE BIOLOGY, 2000, 6 :141-159
[9]   Cadmium is an inducer of oxidative stress in yeast [J].
Brennan, RJ ;
Schiestl, RH .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1996, 356 (02) :171-178
[10]   Complete genome sequence of the ammonia-oxidizing bacterium and obligate chemolithoautotroph Nitrosomonas europaea [J].
Chain, P ;
Lamerdin, J ;
Larimer, F ;
Regala, W ;
Lao, V ;
Land, M ;
Hauser, L ;
Hooper, A ;
Klotz, M ;
Norton, J ;
Sayavedra-Soto, L ;
Arciero, D ;
Hommes, N ;
Whittaker, M ;
Arp, D .
JOURNAL OF BACTERIOLOGY, 2003, 185 (09) :2759-2773