Lee S Y, Chang H N
Department of Chemical Engineering, Korea Advanced Institute of Science and Technology, Yusong-gu, Taejon.
Can J Microbiol. 1995;41 Suppl 1:207-15. doi: 10.1139/m95-189.
A number of Escherichia coli strains including K12, B, W, XL1-Blue, DH5 alpha, HB101, JM109, and C600 were transformed with the stable high-copy-number plasmid pSYL105 containing the Alcaligenes eutrophus polyhydroxyalkanoic acid biosynthesis genes, and were subsequently compared for their ability to synthesize and accumulate poly(3-hydroxybutyric acid) (PHB). The rate of PHB synthesis, the extent of PHB accumulation, and PHB yield from glucose varied considerably from one strain to another. Strains XL1-Blue and B harboring pSYL105 synthesized PHB at the highest rate to a final concentration of ca. 7 g/L in complex medium containing 20 g glucose/L. With an aim to reduce the cost of the medium, the effect on PHB accumulation of supplementing a defined medium with complex nitrogen sources was examined. A PHB concentration of 81 g/L could be obtained in 41 h from a pH-stat fed-batch culture of XL1-Blue(pSYL105) in a semidefined medium. When the availability of acetyl-CoA was increased by supplementing the medium with complex nitrogen sources, amino acids, or oleic acid, PHB synthesis by recombinant E. coli was enhanced.
包括K12、B、W、XL1 - Blue、DH5α、HB101、JM109和C600在内的多种大肠杆菌菌株用含有嗜水气单胞菌聚羟基链烷酸生物合成基因的稳定高拷贝数质粒pSYL105进行转化,随后比较它们合成和积累聚(3 - 羟基丁酸)(PHB)的能力。PHB的合成速率、积累程度以及葡萄糖产生的PHB产量在不同菌株之间差异很大。携带pSYL105的XL1 - Blue和B菌株在含有20 g/L葡萄糖的复合培养基中以最高速率合成PHB,最终浓度约为7 g/L。为了降低培养基成本,研究了用复合氮源补充限定培养基对PHB积累的影响。在半限定培养基中对XL1 - Blue(pSYL105)进行pH值控制补料分批培养,41小时内可获得81 g/L的PHB浓度。当通过用复合氮源、氨基酸或油酸补充培养基来提高乙酰辅酶A的可用性时,重组大肠杆菌的PHB合成得到增强。