Department of Biotechnology, University of Chemistry and Technology Prague, Technicka 5, 166 28, Prague, Czech Republic.
Wageningen Food and Biobased Research, Wageningen University and Research, Bornse Weilanden 9, 6708 WG, Wageningen, The Netherlands.
Appl Microbiol Biotechnol. 2017 Nov;101(22):8279-8291. doi: 10.1007/s00253-017-8555-3. Epub 2017 Oct 8.
The production of acetone, butanol and ethanol by fermentation of renewable biomass has potential to become a valuable industrial process. Mechanisms of solvent production and sporulation involve some common regulators in some ABE-producing clostridia, although details of the links between the pathways are not clear. In this study, we compare a wild-type (WT) Clostridium beijerinckii NRRL B-598 with its mutant strain OESpo0A, in which the gene encoding Spo0A, an important regulator of both sporulation and solventogenesis, is overexpressed in terms of solvent and acid production. We also compare morphologies during growth on two different media: TYA broth, where the WT culture sporulates, and RCM, where the WT culture does not. In addition, RT-qPCR-based analysis of expression profiles of spo0A, spoIIE, sigG, spoVD, ald and buk1 genes involved in sporulation or solvent production in these strains, were compared. The OESpo0A mutant did not produce spores and butanol titre was lower compared to the WT, but increased amounts of butyric acid and ethanol were produced. The gene spo0A had high levels of expression in the WT under non-sporulating culture conditions while other selected genes for sporulation factors were downregulated significantly. Similar observations were obtained for OESpo0A where spo0A overexpression and downregulation of other sporulation genes were demonstrated. Higher expression of spo0A led to higher expression of buk1 and ald, which could confirm the role of spo0A in activation of the solventogenic pathway, although solvent production was not affected significantly in the WT and was weakened in the OESpo0A mutant.
可再生生物质发酵生产丙酮、丁醇和乙醇具有成为有价值的工业过程的潜力。ABE 生产梭菌中一些溶剂生产和孢子形成机制涉及一些共同的调节剂,尽管途径之间的联系细节尚不清楚。在这项研究中,我们比较了野生型(WT)凝结芽孢杆菌 NRRL B-598与其突变株 OESpo0A,后者中编码 Spo0A 的基因过表达,Spo0A 是孢子形成和溶剂形成的重要调节剂。我们还比较了在两种不同培养基上生长时的形态:TYA 肉汤,WT 培养物在这里形成孢子,而 RCM 则不形成孢子。此外,还比较了这些菌株中参与孢子形成或溶剂生产的 spo0A、spoIIE、sigG、spoVD、ald 和 buk1 基因的 RT-qPCR 分析表达谱。与 WT 相比,OESpo0A 突变体不产生孢子,丁醇产量较低,但产生了更多的丁酸和乙醇。在非孢子形成培养条件下,WT 中 spo0A 基因表达水平较高,而其他选择的孢子形成因子基因则显著下调。在 OESpo0A 中也观察到了类似的结果,其中 spo0A 过表达和其他孢子形成基因下调。spo0A 的高表达导致了 buk1 和 ald 的高表达,这可以证实 spo0A 在激活溶剂形成途径中的作用,尽管 WT 中的溶剂产量没有受到显著影响,而 OESpo0A 突变体中的溶剂产量减弱。