Stols L, Donnelly M I
Environmental Research Division, Argonne National Laboratory, Illinois 60439, USA.
Appl Environ Microbiol. 1997 Jul;63(7):2695-701. doi: 10.1128/aem.63.7.2695-2701.1997.
NAD(+)-dependent malic enzyme was cloned from the Escherichia coli genome by PCR based on the published partial sequence of the gene. The enzyme was overexpressed and purified to near homogeneity in two chromatographic steps and was analyzed kinetically in the forward and reverse directions. The Km values determined in the presence of saturating cofactor and manganese ion were 0.26 mM for malate (physiological direction) and 16 mM for pyruvate (reverse direction). When malic enzyme was induced under appropriate culture conditions in a strain of E. coli that was unable to ferment glucose and accumulated pyruvate, fermentative metabolism of glucose was restored. Succinic acid was the major fermentation product formed. When this fermentation was performed in the presence of hydrogen, the yield of succinic acid increased. The constructed pathway represents an alternative metabolic route for the fermentative production of dicarboxylic acids from renewable feedstocks.
基于已发表的基因部分序列,通过聚合酶链反应(PCR)从大肠杆菌基因组中克隆出烟酰胺腺嘌呤二核苷酸(NAD⁺)依赖性苹果酸酶。该酶经两步色谱法实现过表达并纯化至近乎均一状态,并对其正向和反向反应进行了动力学分析。在存在饱和辅因子和锰离子的情况下测定的苹果酸(生理方向)的米氏常数(Km)为0.26 mM,丙酮酸(反向方向)的Km值为16 mM。当在无法发酵葡萄糖且积累丙酮酸的大肠杆菌菌株中,在适当的培养条件下诱导苹果酸酶时,葡萄糖的发酵代谢得以恢复。琥珀酸是形成的主要发酵产物。当在有氢气存在的情况下进行这种发酵时,琥珀酸的产量增加。构建的途径代表了一种从可再生原料发酵生产二羧酸的替代代谢途径。