State Key Laboratory of Bioreactor Engineering, College of Biotechnology, East China University of Science and Technology, No. 130 Meilong Road, Shanghai, People's Republic of China.
Bioprocess Biosyst Eng. 2011 May;34(4):493-8. doi: 10.1007/s00449-010-0493-8. Epub 2010 Dec 10.
A new sialidase-producing strain isolated from soil was identified as Oerskovia xanthineolytica YZ-2. Sialidase was produced when Oerskovia xanthineolytica YZ-2 was exposed to polysialogangliosides. The sialidase of Oerskovia xanthineolytica YZ-2 hydrolyzed sialic acid linkages in polysialogangliosides, and released monosialotetrahexosylganglioside (GM1). The sialidase had the capability of product specificity because it did not attack the sialic acid linkage in GM1. Therefore, Oerskovia xanthineolytica YZ-2 was used for GM1 production from polysialogangliosides. In flasks cultivation phase, it was proved that Oerskovia xanthineolytica YZ-2 could convert polysialogangliosides to GM1 efficiently. Scaling-up the bioprocess with 8% crude ganglioside, polysialogangliosides was converted to GM1 by Oerskovia xanthineolytica YZ-2 in 30 L bioreactor after 18 h. The relative content of GM1 increased from 16.3% in crude ganglioside to 83.7% after Oerskovia xanthineolytica YZ-2 conversion. Therefore, a simple, large-scale conversion process for GM1 production from polysialogangliosides was achieved using Oerskovia xanthineolytica YZ-2 as a biocatalyst.
从土壤中分离到的一株产唾液酸酶的新菌株被鉴定为黄嘌呤氧化不动杆菌 YZ-2。当黄嘌呤氧化不动杆菌 YZ-2 暴露于多唾液酸神经节苷脂时,会产生唾液酸酶。黄嘌呤氧化不动杆菌 YZ-2 的唾液酸酶水解多唾液酸神经节苷脂中的唾液酸键,释放出单唾液酸四己糖神经节苷脂(GM1)。该唾液酸酶具有产物特异性,因为它不会攻击 GM1 中的唾液酸键。因此,黄嘌呤氧化不动杆菌 YZ-2 被用于从多唾液酸神经节苷脂生产 GM1。在摇瓶培养阶段,证明黄嘌呤氧化不动杆菌 YZ-2 能够有效地将多唾液酸神经节苷脂转化为 GM1。在 8%粗神经节苷脂的生物过程放大阶段,在 30 L 生物反应器中,经过 18 h,黄嘌呤氧化不动杆菌 YZ-2 将多唾液酸神经节苷脂转化为 GM1。GM1 的相对含量从粗神经节苷脂中的 16.3%增加到黄嘌呤氧化不动杆菌 YZ-2 转化后的 83.7%。因此,使用黄嘌呤氧化不动杆菌 YZ-2 作为生物催化剂,从多唾液酸神经节苷脂生产 GM1 实现了一种简单、大规模的转化过程。