Lan Xiang, Bao Wenna, Pan Haifeng, Xie Zhipeng, Zhang Jianguo
Sheng Wu Gong Cheng Xue Bao. 2014 Feb;30(2):315-9.
The cis-epoxysuccinate hydrolase (CESH) from Rhizobium strain BK-20 is the key enzyme for L(+)-tartaric acid production. To establish a highly efficient and stable production process, we first optimized the enzyme production from Rhizobium strain BK-20, and then developed an immobilized cell-culture process for sustained production of L(+)-tartaric acid. The enzyme activity of free cells reached (3 498.0 +/- 142.6) U/g, and increased by 643% after optimization. The enzyme activity of immobilized cells reached (2 817.2 +/- 226.7) U/g, under the optimal condition with sodium alginate as carrier, cell concentration at 10% (W/V) and gel concentration at 1.5% (W/V). The immobilized cells preserved high enzyme activity and normal structure after 10 repeated batches. The conversion rate of the substrate was more than 98%, indicating its excellent production stability.
来自根瘤菌菌株BK - 20的顺式环氧琥珀酸水解酶(CESH)是生产L(+) - 酒石酸的关键酶。为建立高效稳定的生产工艺,我们首先优化了根瘤菌菌株BK - 20的酶生产,然后开发了一种固定化细胞培养工艺以持续生产L(+) - 酒石酸。游离细胞的酶活性达到(3498.0±142.6) U/g,优化后提高了643%。在以海藻酸钠为载体、细胞浓度为10%(W/V)、凝胶浓度为1.5%(W/V)的最佳条件下,固定化细胞的酶活性达到(2817.2±226.7) U/g。经过10次重复批次后,固定化细胞保持了高酶活性和正常结构。底物转化率超过98%,表明其具有优异的生产稳定性。