Gungormusler-Yilmaz Mine, Shamshurin Dmitry, Grigoryan Marine, Taillefer Marcel, Spicer Victor, Krokhin Oleg V, Sparling Richard, Levin David B
Department of Biosystems Engineering, Faculty of Engineering, University of Manitoba, Manitoba, Winnipeg R3T 5 V6, MB, Canada ; Department of Bioengineering, Ege University, Izmir, Turkey.
Manitoba Centre for Proteomics and Systems Biology, University of Manitoba, Winnipeg, Manitoba, Canada.
AMB Express. 2014 Aug 30;4:63. doi: 10.1186/s13568-014-0063-6. eCollection 2014.
Higher initial glycerol loadings (620 mM) have a negative effect on growth and 1,3-propanediol (1,3-PDO) synthesis in Clostridium butyricum DSM 10702 relative to lower initial glycerol concentrations (170 mM). To help understand metabolic shifts associated with elevated glycerol, protein expression levels were quantified by LC/MS/MS analyses. Thirty one (31) proteins involved in conversion of glycerol to 1,3-PDO and other by-products were analyzed by multiple reaction monitoring (MRM). The analyses revealed that high glycerol concentrations reduced cell growth. The expression levels of most proteins in glycerol catabolism pathways were down-regulated, consistent with the slower growth rates observed. However, at high initial glycerol concentrations, some of the proteins involved in the butyrate synthesis pathways such as a putative ethanol dehydrogenase (CBY_3753) and a 3-hydroxybutyryl-CoA dehydrogenase (CBY_3045) were up-regulated in both exponential and stationary growth phases. Expression levels of proteins (CBY_0500, CBY_0501 and CBY_0502) involved in the reductive pathway of glycerol to 1,3-PDO were consistent with glycerol consumption and product concentrations observed during fermentation at both glycerol concentrations, and the molar yields of 1,3-PDO were similar in both cultures. This is the first report that correlates expression levels of glycerol catabolism enzymes with synthesis of 1,3-PDO in C. butyricum. The results revealed that significant differences in the expression of a small subset of proteins were observed between exponential and stationary growth phases at both low and high glycerol concentrations.
与较低的初始甘油浓度(170 mM)相比,较高的初始甘油负载量(620 mM)对丁酸梭菌DSM 10702的生长和1,3 - 丙二醇(1,3 - PDO)合成具有负面影响。为了帮助理解与甘油浓度升高相关的代谢变化,通过液相色谱/串联质谱(LC/MS/MS)分析对蛋白质表达水平进行了定量。通过多反应监测(MRM)分析了31种参与甘油转化为1,3 - PDO和其他副产物的蛋白质。分析表明,高甘油浓度会降低细胞生长。甘油分解代谢途径中大多数蛋白质的表达水平下调,这与观察到的较慢生长速率一致。然而,在高初始甘油浓度下,一些参与丁酸合成途径的蛋白质,如假定的乙醇脱氢酶(CBY_3753)和3 - 羟基丁酰 - CoA脱氢酶(CBY_3045),在指数生长期和稳定生长期均上调。参与甘油还原途径生成1,3 - PDO的蛋白质(CBY_0500、CBY_0501和CBY_0502)的表达水平与两种甘油浓度下发酵过程中观察到的甘油消耗和产物浓度一致,并且两种培养物中1,3 - PDO的摩尔产率相似。这是第一份将丁酸梭菌中甘油分解代谢酶的表达水平与1,3 - PDO合成相关联的报告。结果表明,在低甘油浓度和高甘油浓度下,指数生长期和稳定生长期之间一小部分蛋白质的表达存在显著差异。