Chien Liang-Jung, Lee Cheng-Kang
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan.
Biotechnol Prog. 2007 Sep-Oct;23(5):1017-22. doi: 10.1021/bp070036w. Epub 2007 Aug 11.
Bacillus subtilis strains that can produce hyaluronic acid (HA) were constructed by integrating the HA synthase gene (hasA) and the UDP-glucose dehydrogenase gene of group C Streptococcus (hasB) or of B. subtilis itself (tauD) into the amyE locus of the B. subtilis chromosome. All of the inserted genes were under the control of a strong constitutive vegII promoter of B. subtilis. Although HA production could be achieved by expressing hasA alone, coexpressing hasB or tauD with hasA could enhance HA production at least 2-fold. To replenish the energy consumed for HA biosynthesis, Vitreoscilla hemoglobin (VHb) was coexpressed with the HA-expressing genes. With the expression of VHb, not only the cell concentration was enhanced 25%, but also HA production was further increased by 100%. About 1.8 g/L of HA was obtained by the recombinant strain B. subtilis carrying VHb, hasA, and tauD genes in the expression cassette after 30 h cultivation.
通过将透明质酸合成酶基因(hasA)以及C组链球菌的UDP - 葡萄糖脱氢酶基因(hasB)或枯草芽孢杆菌自身的UDP - 葡萄糖脱氢酶基因(tauD)整合到枯草芽孢杆菌染色体的amyE位点,构建了能够产生透明质酸(HA)的枯草芽孢杆菌菌株。所有插入基因均受枯草芽孢杆菌强组成型vegII启动子的控制。虽然单独表达hasA就能实现HA的产生,但将hasB或tauD与hasA共表达可使HA产量至少提高2倍。为补充HA生物合成所消耗的能量,将透明颤菌血红蛋白(VHb)与表达HA的基因共表达。随着VHb的表达,不仅细胞浓度提高了25%,而且HA产量进一步提高了100%。培养30小时后,携带VHb、hasA和tauD基因的重组枯草芽孢杆菌菌株在表达盒中获得了约1.8 g/L的HA。