Institute of Biochemistry and Biophysics - Polish Academy of Sciences, Pawińskiego 5a, 02-106, Warsaw, Poland.
Institute of Agricultural and Food Biotechnology, Rakowiecka 36, 02-532, Warsaw, Poland.
Microb Cell Fact. 2019 Feb 13;18(1):36. doi: 10.1186/s12934-019-1085-1.
Interactions between microorganisms during specific steps of anaerobic digestion determine metabolic pathways in bioreactors and consequently the efficiency of fermentation processes. This study focuses on conversion of lactate and acetate to butyrate by bacteria of dark fermentation. The recently recognized flavin-based electron bifurcation as a mode of energy coupling by anaerobes increases our knowledge of anaerobic lactate oxidation and butyrate formation.
Microbial communities from dark fermentation bioreactors or pure culture of Clostridium butyricum are able to convert lactate and acetate to butyrate in batch experiments. The ability of C. butyricum to transform lactate and acetate to butyrate was shown for the first time, with ethanol identified as an additional end product of this process. A search for genes encoding EtfAB complexes and their gene neighbourhood in C. butyricum and other bacteria capable of lactate and acetate conversion to butyrate as well as butyrate-producers only and the lactate oxidiser Acetobacterium woodii, revealed that the Etf complexes involved in (i) lactate oxidation and (ii) butyrate synthesis, form separate clusters. There is a more extent similarity between Etf subunits that are involved in lactate oxidation in various species (e.g. A. woodii and C. butyricum) than between the different etf gene products within the same species of butyrate producers. A scheme for the metabolic pathway of lactate and acetate transformation to butyrate in C. butyricum was constructed.
Studies on the conversion of lactate and acetate to butyrate by microbial communities from dark fermentation bioreactors or Clostridium butyricum suggest that a phenomenon analogous to cross-feeding of lactate in gastrointestinal tract also occurs in hydrogen-yielding reactors. A scheme of lactate and acetate transformation pathway is proposed, based on the example of C. butyricum, which employs flavin-based electron bifurcation. This process utilizes electron-transferring flavoprotein (Etf) complexes specific for (i) lactate oxidation and (ii) butyrate formation. Phylogenetic analysis revealed that such complexes are encoded in the genomes of other bacteria capable of lactate and acetate conversion to butyrate. These findings contribute significantly to our understanding of the metabolic pathways and symbiotic interactions between bacteria during the acidogenic step of anaerobic digestion.
在厌氧消化的特定步骤中,微生物之间的相互作用决定了生物反应器中的代谢途径,进而影响发酵过程的效率。本研究关注于细菌对乳酸和乙酸向丁酸的转化。最近发现的基于黄素的电子分叉作为厌氧菌的一种能量偶联模式,增加了我们对厌氧乳酸氧化和丁酸形成的认识。
来自黑暗发酵生物反应器的微生物群落或纯培养的丁酸梭菌能够在批处理实验中将乳酸和乙酸转化为丁酸。首次证明丁酸梭菌能够将乳酸和乙酸转化为丁酸,同时鉴定出乙醇是该过程的另一种终产物。对编码 EtfAB 复合物及其基因邻域的基因在丁酸梭菌和其他能够将乳酸和乙酸转化为丁酸的细菌以及丁酸产生菌和乳酸氧化菌丙酮丁醇梭菌中的搜索,表明参与(i)乳酸氧化和(ii)丁酸合成的 Etf 复合物形成单独的簇。在不同物种(如丙酮丁醇梭菌和丁酸梭菌)中参与乳酸氧化的 Etf 亚基之间的相似度要高于同一丁酸产生菌内不同的 etf 基因产物之间的相似度。构建了丁酸梭菌中乳酸和乙酸转化为丁酸的代谢途径示意图。
对来自黑暗发酵生物反应器或丁酸梭菌的微生物群落将乳酸和乙酸转化为丁酸的研究表明,类似于胃肠道中乳酸的交叉喂养现象也发生在产氢反应器中。提出了基于丁酸梭菌的乳酸和乙酸转化途径的方案,该方案利用了基于黄素的电子分叉。该过程利用了特定于(i)乳酸氧化和(ii)丁酸形成的电子转移黄素蛋白(Etf)复合物。系统发育分析表明,其他能够将乳酸和乙酸转化为丁酸的细菌的基因组中也编码了这些复合物。这些发现极大地促进了我们对厌氧消化产酸阶段细菌代谢途径和共生相互作用的理解。