Brinkmann U, Babel W
Abteilung Biotechnologie, Universität Leipzig, Germany.
Appl Microbiol Biotechnol. 1996 Mar;45(1-2):217-23. doi: 10.1007/s002530050673.
A bacterium classified as Rhodococcus opacus, which is able to use pyridine (a potentially growth-inhibiting substrate) as its sole source of carbon, energy and nitrogen, was isolated. In a carbon-limited chemostat culture, the kinetics was determined for growth on both pyridine and a mixture of pyridine and fructose (9 mM/22.15 mM). With growth on pyridine, stable steady states were achieved up to dilution rates of about 0.1 h-1. A further increase in the dilution rate resulted in the progressive accumulation of pyridine in the culture liquid and the cells were washed out. The maximum specific growth rate (mu max = 0.23 h-1) and the Ks value (0.22 mM) for growth on pyridine were determined from the residual pyridine concentrations measured within the range of stable steady states. With growth on the substrate mixture, the specific pyridine consumption rates and the residual pyridine concentrations were lower at similar dilution rates than with growth on pyridine alone, and stable steady states were established at dilution rates of up to 0.13 h-1. The maximum pyridine degradation rate was enhanced to 270 mg pyridine l-1 h-1 compared to 210 mg pyridine l-1 h-1 with growth on pyridine as a single substrate. An external nitrogen source did not need to be added in the case of growth on the substrate mixture. Fructose was assimilated by means of ammonium released from pyridine. Analysis of the nitrogen balance furnished proof that pyridine is an energy-deficient substrate; pyridine was assimilated and dissimilated at a ratio of 1 mol/0.67 mol respectively. The resulting yield coefficient was about 0.55 g dry weight/g pyridine. Moreover, it was demonstrated that, in regard to the biologically usable energy, 1 mol pyridine corresponds to 0.43 mol fructose.
分离出了一种被归类为不透明红球菌的细菌,它能够将吡啶(一种潜在的生长抑制性底物)作为其唯一的碳、能量和氮源。在碳限制恒化器培养中,测定了在吡啶以及吡啶和果糖混合物(9 mM/22.15 mM)上生长的动力学。在以吡啶为底物生长时,直到稀释率约为0.1 h-1时都能达到稳定的稳态。稀释率进一步增加导致吡啶在培养液中逐渐积累,细胞被冲出。根据在稳定稳态范围内测得的残留吡啶浓度,确定了在吡啶上生长的最大比生长速率(μm ax = 0.23 h-1)和Ks值(0.22 mM)。在以底物混合物为底物生长时,在相似的稀释率下,比吡啶消耗速率和残留吡啶浓度比单独以吡啶为底物生长时更低,并且在高达0.13 h-1的稀释率下建立了稳定的稳态。与以吡啶为单一底物生长时的210 mg吡啶 l-1 h-1相比,最大吡啶降解速率提高到了270 mg吡啶 l-1 h-1。在以底物混合物为底物生长的情况下,不需要添加外部氮源。果糖通过吡啶释放的铵被同化。氮平衡分析证明吡啶是一种能量不足的底物;吡啶分别以1 mol/0.67 mol的比例被同化和异化。由此产生的产率系数约为0.55 g干重/g吡啶。此外,还证明了,就生物可利用能量而言,1 mol吡啶相当于0.43 mol果糖。