Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, Jiangnan University, Wuxi, China.
Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi, China.
Biotechnol Bioeng. 2018 Feb;115(2):483-494. doi: 10.1002/bit.26478. Epub 2017 Dec 1.
Acid stress induced by the accumulation of organic acids during the fermentation of propionibacteria is a severe limitation in the microbial production of propionic acid (PA). To enhance the acid resistance of strains, the tolerance mechanisms of cells must first be understood. In this study, comparative genomic and transcriptomic analyses were conducted on wild-type and acid-tolerant Propionibacterium acidipropionici to reveal the microbial response of cells to acid stress during fermentation. Combined with the results of previous proteomic and metabolomic studies, several potential acid-resistance mechanisms of P. acidipropionici were analyzed. Energy metabolism and transporter activity of cells were regulated to maintain pH homeostasis by balancing transmembrane transport of protons and ions; redundant protons were eliminated by enhancing the metabolism of certain amino acids for a relatively stable intracellular microenvironment; and protective mechanism of macromolecules were also induced to repair damage to proteins and DNA by acids. Transcriptomic data indicated that the synthesis of acetate and lactate were undesirable in the acid-resistant mutant, the expression of which was 2.21-fold downregulated. In addition, metabolomic data suggested that the accumulation of lactic acid and acetic acid reduced the carbon flow to PA and led to a decrease in pH. On this basis, we propose a metabolic engineering strategy to regulate the synthesis of lactic acid and acetic acid that will reduce by-products significantly and increase the PA yield by 12.2% to 10.31 ± 0.84 g/g DCW. Results of this study provide valuable guidance to understand the response of bacteria to acid stress and to construct microbial cell factories to produce organic acids by combining systems biology technologies with synthetic biology tools.
在丙酸杆菌发酵过程中有机酸的积累会导致酸胁迫,这是丙酸(PA)微生物生产的严重限制。为了提高菌株的耐酸能力,首先必须了解细胞的耐受机制。在这项研究中,对野生型和耐酸丙酸丙酸杆菌进行了比较基因组学和转录组学分析,以揭示细胞在发酵过程中对酸胁迫的微生物响应。结合以前的蛋白质组学和代谢组学研究结果,分析了丙酸丙酸杆菌的几种潜在耐酸机制。通过平衡质子和离子的跨膜运输来调节细胞的能量代谢和转运体活性,以维持 pH 平衡;通过增强某些氨基酸的代谢来消除多余的质子,从而保持相对稳定的细胞内微环境;并诱导大分子的保护机制,通过酸来修复蛋白质和 DNA 的损伤。转录组数据表明,耐酸突变体中乙酸和乳酸的合成是不可取的,其表达水平下调了 2.21 倍。此外,代谢组学数据表明,乳酸和乙酸的积累减少了流向 PA 的碳流,导致 pH 值下降。在此基础上,我们提出了一种代谢工程策略来调节乳酸和乙酸的合成,这将显著减少副产物,并将 PA 产量提高 12.2%至 10.31±0.84 g/g DCW。本研究结果为理解细菌对酸胁迫的响应提供了有价值的指导,并为通过系统生物学技术与合成生物学工具构建微生物细胞工厂生产有机酸提供了依据。