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基于壳聚糖亲和固定化的工程化平台用于生产低分子量肝素。

An engineered platform based on chitin-affinity immobilization for producing low molecular weight heparin.

机构信息

School of Pharmaceutical Science, Jiangnan University, Wuxi 214122, China.

College of Chemistry & Molecule Sciences, Wuhan University, Wuhan 430072, China.

出版信息

Carbohydr Polym. 2017 Dec 1;177:297-305. doi: 10.1016/j.carbpol.2017.08.134. Epub 2017 Sep 19.

Abstract

Using chitin-affinity interaction between triple-functional heparinase I (Hep I) and chitin, an engineered platform was prepared to produce controllable low molecular weight heparin (LMWH). Chitin microspheres with well-defined nanofibrils were fabricated through a "bottom up" pathway. An enhanced soluble protein, ChBD-SUMO-Hep I (CSH-I), was expressed in 3L batch fermentation with a high bioactivity of 2.5×10 IU/L. Chitin binding domain (ChBD) can specifically bind to chitin in noncovalent way, which leads to the immobilization and purification of enzyme in a single step. The immobilized CSH-I was preferred over its free counterpart due to its higher tolerance to heat and pH, as well as improved shelf-life. The restraint enzyme could be reused up to 8 times to achieve a conversion yield exceeding 90%. By using the bioinspired conjugates, the qualified LMWH fractions were obtained by monitoring the degradation process with an absorbance range of 44.5-68.3 at 232nm.

摘要

利用三重功能肝素酶 I(Hep I)与壳聚糖之间的亲和作用,制备了一种工程化平台,用于生产可控的低分子量肝素(LMWH)。通过“自下而上”的途径制备了具有明确定义的纳米纤维的壳聚糖微球。通过 3L 批式发酵表达了增强型可溶性蛋白 ChBD-SUMO-Hep I(CSH-I),其生物活性高达 2.5×10 IU/L。壳聚糖结合结构域(ChBD)可以与壳聚糖以非共价方式特异性结合,从而在一步中实现酶的固定化和纯化。固定化 CSH-I 比游离酶具有更高的热稳定性和 pH 耐受性,以及更长的保质期。固定化酶可重复使用 8 次以上,转化率超过 90%。通过使用仿生缀合物,通过监测 232nm 处 44.5-68.3 的吸光度范围,获得了合格的 LMWH 级分。

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