Htet April N, Noguchi Mana, Ninomiya Kazuaki, Tsuge Yota, Kuroda Kosuke, Kajita Shinya, Masai Eiji, Katayama Yoshihiro, Shikinaka Kazuhiro, Otsuka Yuichiro, Nakamura Masaya, Honda Ryo, Takahashi Kenji
Institute of Science and Engineering, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan; Department of Chemical Engineering, Mandalay Technological University, Mandalay, Myanmar.
Institute of Science and Engineering, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.
J Biosci Bioeng. 2018 Jun;125(6):717-722. doi: 10.1016/j.jbiosc.2017.12.026. Epub 2018 Feb 1.
Actual biomass of microalgae was tested as a fermentation substrate for microbial production of 2-pyrone 4,6-dicarboxylic acid (PDC). Acid-hydrolyzed green microalgae Chlorella emersonii (algae hydrolysate) was diluted to adjust the glucose concentration to 2 g/L and supplemented with the nutrients of Luria-Bertani (LB) medium (tryptone 10 g/L and yeast extract 5 g/L). When the algae hydrolysate was used as a fermentation source for recombinant Escherichia coli producing PDC, 0.43 g/L PDC was produced with a yield of 20.1% (mol PDC/mol glucose), whereas 0.19 g/L PDC was produced with a yield of 8.6% when LB medium supplemented with glucose was used. To evaluate the potential of algae hydrolysate alone as a fermentation medium for E. coli growth and PDC production, the nutrients of LB medium were reduced from the algae hydrolysate medium. Interestingly, 0.17 g/L PDC was produced even without additional nutrient, which was comparable to the case using pure glucose medium with nutrients of LB medium. When using a high concentration of hydrolysate without additional nutrients, 1.22 g/L PDC was produced after a 24-h cultivation with the yield of 16.1%. Overall, C. emersonii has high potential as cost-effective fermentation substrate for the microbial production of PDC.
对微藻的实际生物量作为微生物生产2-吡喃酮-4,6-二羧酸(PDC)的发酵底物进行了测试。将酸水解的绿色微藻艾氏小球藻(藻类水解产物)稀释以将葡萄糖浓度调节至2 g/L,并补充了Luria-Bertani(LB)培养基的营养成分(胰蛋白胨10 g/L和酵母提取物5 g/L)。当藻类水解产物用作生产PDC的重组大肠杆菌的发酵源时,产生了0.43 g/L的PDC,产率为20.1%(摩尔PDC/摩尔葡萄糖),而当使用补充了葡萄糖的LB培养基时,产生了0.19 g/L的PDC,产率为8.6%。为了评估单独的藻类水解产物作为大肠杆菌生长和PDC生产的发酵培养基的潜力,从藻类水解产物培养基中减少了LB培养基的营养成分。有趣的是,即使没有额外的营养物质也产生了0.17 g/L的PDC,这与使用含有LB培养基营养成分的纯葡萄糖培养基的情况相当。当使用高浓度的水解产物且不添加额外营养物质时,经过24小时培养产生了1.22 g/L的PDC,产率为16.1%。总体而言,艾氏小球藻作为微生物生产PDC的具有成本效益的发酵底物具有很高的潜力。