REQUIMTE/CQFB, Chemistry Department, FCT/ Universidade Nova de Lisboa, 2829-516 Caparica, Portugal.
REQUIMTE/CQFB, Chemistry Department, FCT/ Universidade Nova de Lisboa, 2829-516 Caparica, Portugal.
N Biotechnol. 2014 Jun 25;31(4):335-44. doi: 10.1016/j.nbt.2013.06.008. Epub 2013 Aug 9.
In this work, we present a dynamic metabolic model that describes the uptake of complex mixtures of volatile fatty acids (VFA) and respective conversion into PHA by mixed microbial cultures (MMC). This model builds upon a previously published flux balance analysis model [1] that identified the minimization of TCA cycle activity as the key metabolic objective to predict PHA storage fluxes and respective composition. The model was calibrated either with experimental data of PHA production from fermented sugar cane molasses or from synthetic mixtures of VFA. All PHA production experiments were performed using a MMC selected with fermented sugar cane molasses under feast and famine regimen. The model was able to capture the process dynamics denoted by an excellent fit between experimental and computed time profiles of concentrations with the regression coefficients always above 0.92. The introduced VFA uptake regulatory factor reflects the decrease of acetyl-CoA and propionyl-CoA available to TCA cycle in conformity with the hypothesis that the minimization of TCA cycle is a key metabolic objective for MMC subjected to feast and famine regimen for the maximization of PHA production.
在这项工作中,我们提出了一个动态代谢模型,描述了混合微生物培养物(MMC)对复杂混合物的挥发性脂肪酸(VFA)的摄取以及各自转化为 PHA。该模型建立在以前发表的通量平衡分析模型[1]的基础上,该模型确定了 TCA 循环活性的最小化是预测 PHA 储存通量和相应组成的关键代谢目标。该模型通过从发酵甘蔗蜜中生产 PHA 的实验数据或从 VFA 的合成混合物进行了校准。所有 PHA 生产实验均使用在丰食和饥饿条件下从发酵甘蔗蜜中选择的 MMC 进行。该模型能够捕捉到过程动态,表现为实验和计算浓度时间曲线之间的极好拟合,回归系数始终高于 0.92。引入的 VFA 摄取调节因子反映了 TCA 循环中可用的乙酰辅酶 A 和丙酰辅酶 A 的减少,这符合以下假设:即 TCA 循环的最小化是 MMC 的关键代谢目标,MMC 处于丰食和饥饿条件下以最大化 PHA 的生产。