Wong H H, Lee S Y
Department of Chemical Engineering, Advanced Institute of Science and Technology (KAIST), Taejon, Korea.
Appl Microbiol Biotechnol. 1998 Jul;50(1):30-3. doi: 10.1007/s002530051252.
Recombinant Escherichia coli strain GCSC 6576, harboring a high-copy-number plasmid containing the Ralstonia eutropha genes for polyhydroxyalkanoate (PHA) synthesis and the E. coli ftsZ gene, was employed to produce poly-(3-hydroxybutyrate) (PHB) from whey, pH-stat fed-batch fermentation, using whey powder as the nutrient feed, produced cellular dry weight and PHB concentrations of 109 g l-1 and 50 g l-1 respectively in 47 h. When concentrated whey solution containing 210 g l-1 lactose was used as the nutrient feed, cellular dry weight and PHB concentrations of 87 g l-1 and 69 g l-1 respectively could be obtained in 49 h by pH-stat fed-batch culture. The PHB content was as high as 80% of the cellular dry weight. These results suggest that cost-effective production of PHB is possible by fed-batch culture of recombinant E. coli using concentrated whey solution as a substrate.
重组大肠杆菌菌株GCSC 6576含有一个高拷贝数质粒,该质粒包含用于聚羟基脂肪酸酯(PHA)合成的嗜麦芽窄食单胞菌基因和大肠杆菌ftsZ基因,采用该菌株以乳清为原料,通过pH值控制补料分批发酵生产聚(3-羟基丁酸酯)(PHB),使用乳清粉作为营养饲料,在47小时内细胞干重和PHB浓度分别达到109 g l-1和50 g l-1。当使用含有210 g l-1乳糖的浓缩乳清溶液作为营养饲料时,通过pH值控制补料分批培养,在49小时内细胞干重和PHB浓度分别可达87 g l-1和69 g l-1。PHB含量高达细胞干重的80%。这些结果表明,使用浓缩乳清溶液作为底物,通过重组大肠杆菌的补料分批培养可以实现PHB的经济高效生产。