Johnson M R, Conners S B, Montero C I, Chou C J, Shockley K R, Kelly R M
Dept. of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA.
Appl Environ Microbiol. 2006 Jan;72(1):811-8. doi: 10.1128/AEM.72.1.811-818.2006.
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 H2 transfer resulted in three- to fivefold-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.
当嗜热细菌海栖热袍菌(Thermotoga maritima)与嗜热古菌詹氏产甲烷球菌(Methanococcus jannaschii)共培养时,在其转录组中发现了显著的生长阶段依赖性差异。对于海栖热袍菌单培养物从中对数期到早稳定期的转变,有24个基因(占基因组的1.3%)差异表达两倍或更多。相比之下,在相同的生长阶段转变中,产甲烷共培养导致海栖热袍菌中有292个基因在该水平上差异表达(占基因组的15.5%)。种间H2转移导致海栖热袍菌的细胞密度比单培养时高三到五倍,同时形成了基于胞外多糖(EPS)的细胞聚集体。特定sigma因子和与ppGpp依赖性严谨反应相关的基因的差异表达表明其参与了向稳定期的转变和聚集体的形成。细胞聚集是生长阶段依赖性的,在对数中期最为显著,并随着细胞进入稳定期而衰减。细胞聚集的减少与编码形成EPS的糖基转移酶的基因下调以及编码β特异性糖基水解酶的基因上调同时发生;后者可能参与β连接的EPS的水解,以使细胞从聚集体中释放出来。聚集体的分离可能有助于海栖热袍菌在与其他生物共存的自然环境中定殖到新的位置。综上所述,这些结果表明共生相互作用会影响产甲烷共培养中异养生物的转录组,在研究厌氧环境中的微生物生态时应考虑这一因素。