Ahrens K, Menzel K, Zeng A, Deckwer W
GBF-Gesellschaft für Biotechnologische Forschung mbH, Biochemical Engineering Division, Mascheroder Weg 1, D-38124 Braunschweig, Germany.
Biotechnol Bioeng. 1998 Sep 5;59(5):544-52. doi: 10.1002/(sici)1097-0290(19980905)59:5<544::aid-bit3>3.0.co;2-a.
The initial steps of glycerol dissimilation and 1,3-propanediol (1, 3-PD) formation by Klebsiella pneumoniae anaerobically grown on glycerol were studied by quantifying the in vitro and in vivo activities of enzymes in continuous culture under conditions of steady state and oscillation and during transient phases. The enzymes studied included glycerol dehydrogenase (GDH), glycerol dehydratase (GDHt), and 1,3-propanediol oxidoreductase (PDOR). Three conclusions can be drawn from the steady-state results. First, glycerol concentration in the culture is a key parameter that inversely affects the in vitro activities (concentrations) of all three enzymes, but has a positive effect on their in vivo activities. Growth rate significantly affects the ratio of in vitro and in vivo enzyme activities under low glycerol concentrations, but not under glycerol excess. Second, whereas the flux through the oxidative pathway of glycerol dissimilation is governed mainly by the regulation of in vivo enzyme activity on a metabolic level, the flux through the reductive pathway is largely controlled by the synthesis of enzymes. Third, GDHt is a major rate-liming enzyme for the consumption of glycerol and the formation of 1,3-PD in K. pneumoniae at high glycerol concentrations. Results from oscillating cultures revealed that both in vitro and in vivo activities of the enzymes oscillated. The average values of the in vitro activities during an oscillation cycle agreed well with their corresponding values for nonoscillating cultures under similar environmental conditions. Experiments with step changes in the feed concentration of glycerol demonstrated that growth and product formation are very sensitive to changes of substrate concentration in the culture. This sensitivity is due to the dynamic responses of the genetic and metabolic networks. They should be considered when modeling the dynamics of the culture and attempting to improve the formation of 1,3-PD.
通过在稳态、振荡及瞬态阶段的连续培养条件下对酶的体外和体内活性进行定量,研究了肺炎克雷伯菌在甘油上厌氧生长时甘油异化及1,3 - 丙二醇(1,3 - PD)形成的初始步骤。所研究的酶包括甘油脱氢酶(GDH)、甘油脱水酶(GDHt)和1,3 - 丙二醇氧化还原酶(PDOR)。从稳态结果可得出三个结论。首先,培养物中的甘油浓度是一个关键参数,它对所有三种酶的体外活性(浓度)有反向影响,但对其体内活性有正向影响。在低甘油浓度下,生长速率显著影响酶的体外和体内活性之比,但在甘油过量时则不然。其次,虽然通过甘油异化氧化途径的通量主要受代谢水平上体内酶活性的调节,但通过还原途径的通量在很大程度上受酶合成的控制。第三,在高甘油浓度下,GDHt是肺炎克雷伯菌中甘油消耗和1,3 - PD形成的主要限速酶。振荡培养的结果表明,酶的体外和体内活性均发生振荡。振荡周期内体外活性的平均值与其在类似环境条件下非振荡培养的相应值吻合良好。甘油进料浓度阶跃变化的实验表明,生长和产物形成对培养物中底物浓度的变化非常敏感。这种敏感性归因于遗传和代谢网络的动态响应。在对培养物动态进行建模并试图改善1,3 - PD的形成时应考虑这些因素。