The Thermotoga maritima phenotype is impacted by syntrophic interaction with Methanococcus jannaschii in hyperthermophilic coculture

被引:45
作者
Johnson, MR [1 ]
Conners, SB [1 ]
Montero, CI [1 ]
Chou, CJ [1 ]
Shockley, KR [1 ]
Kelly, RM [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
关键词
D O I
10.1128/AEM.72.1.811-818.2006
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
Significant growth phase-dependent differences were noted in the transcriptome of the hyperthermophilic bacterium Thermotoga maritima when it was cocultured with the hyperthermophilic archaeon Methanococcus jannaschii. For the mid-log-to-early-stationary-phase transition of a T. maritima monoculture, 24 genes (1.3% of the genome) were differentially expressed twofold or more. In contrast, methanogenic coculture gave rise to 292 genes differentially expressed in T. maritima at this level (15.5% of the genome) for the same growth phase transition. Interspecies H, transfer resulted in three- to five-fold-higher T. maritima cell densities than in the monoculture, with concomitant formation of exopolysaccharide (EPS)-based cell aggregates. Differential expression of specific sigma factors and genes related to the ppGpp-dependent stringent response suggests involvement in the transition into stationary phase and aggregate formation. Cell aggregation was growth phase dependent, such that it was most prominent during mid-log phase and decayed as cells entered stationary phase. The reduction in cell aggregation was coincidental with down-regulation of genes encoding EPS-forming glycosyltranferases and up-regulation of genes encoding beta-specific glycosyl hydrolases; the latter were presumably involved in hydrolysis of beta-linked EPS to release cells from aggregates. Detachment of aggregates may facilitate colonization of new locations in natural environments where T. maritima coexists with other organisms. Taken together, these results demonstrate that syntrophic interactions can impact the transcriptome of heterotrophs in methanogenic coculture, and this factor should be considered in examining the microbial ecology in anaerobic environments.
引用
收藏
页码:811 / 818
页数:8
相关论文
共 54 条
[11]   The involvement of cell-to-cell signals in the development of a bacterial biofilm [J].
Davies, DG ;
Parsek, MR ;
Pearson, JP ;
Iglewski, BH ;
Costerton, JW ;
Greenberg, EP .
SCIENCE, 1998, 280 (5361) :295-298
[12]   Characterization of filamentous foaming in activated sludge systems using oligonucleotide hybridization probes and antibody probes [J].
de los Reyes, FL ;
Oerther, DB ;
de los Reyes, MF ;
Hernandez, M ;
Raskin, L .
WATER SCIENCE AND TECHNOLOGY, 1998, 37 (4-5) :485-493
[13]   DnaK dependence of mutant ethanol oxidoreductases evolved for aerobic function and protective role of the chaperone against protein oxidative damage in Escherichia coli [J].
Echave, P ;
Esparza-Cerón, MA ;
Cabiscol, E ;
Tamarit, J ;
Ros, J ;
Membrillo-Hernández, J ;
Lin, ECC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (07) :4626-4631
[14]   Role of the Escherichia coli FadR regulator in stasis survival and growth phase-dependent expression of the uspA, fad, and fab genes [J].
Farewell, A ;
Diez, AA ;
DiRusso, CC ;
Nystrom, T .
JOURNAL OF BACTERIOLOGY, 1996, 178 (22) :6443-6450
[15]   Regulation by nutrient limitation [J].
Ferenci, T .
CURRENT OPINION IN MICROBIOLOGY, 1999, 2 (02) :208-213
[16]   THERMOTOGA-MARITIMA SP-NOV REPRESENTS A NEW GENUS OF UNIQUE EXTREMELY THERMOPHILIC EUBACTERIA GROWING UP TO 90-DEGREES-C [J].
HUBER, R ;
LANGWORTHY, TA ;
KONIG, H ;
THOMM, M ;
WOESE, CR ;
SLEYTR, UB ;
STETTER, KO .
ARCHIVES OF MICROBIOLOGY, 1986, 144 (04) :324-333
[18]   Population density-dependent regulation of exopolysaccharide formation in the hyperthermophilic bacterium Thermotoga maritima [J].
Johnson, MR ;
Montero, CI ;
Conners, SB ;
Shockley, KR ;
Bridger, SL ;
Kelly, RM .
MOLECULAR MICROBIOLOGY, 2005, 55 (03) :664-674
[19]   Detachment of Actinobacillus actinomycetemcomitans biofilm cells by an endogenous β-hexosaminidase activity [J].
Kaplan, JB ;
Ragunath, C ;
Ramasubbu, N ;
Fine, DH .
JOURNAL OF BACTERIOLOGY, 2003, 185 (16) :4693-4698
[20]  
Kerr M K, 2001, Biostatistics, V2, P183, DOI 10.1093/biostatistics/2.2.183