Department of Experimental Medicine, Section of Biotechnology and Molecular Biology, University of Campania "Luigi Vanvitelli", Via De Crecchio 7, 80138, Naples, Italy.
Appl Microbiol Biotechnol. 2019 Aug;103(16):6771-6782. doi: 10.1007/s00253-019-09969-8. Epub 2019 Jun 20.
Heparin and chondroitin sulfate are used as anti-thrombic and anti-osteoarthritis drugs, respectively, but their pharmacological actions depend on their structural characteristics such as their sulfation grade and their molecular weight. In the last years, new fermentation-based biotechnological approaches have tried to obtain heparin and chondroitin sulfate starting from the heparosan and chondroitin-like capsular polysaccharides produced by Escherichia coli K5 and K4. The study of the microbial capsular polysaccharide molecular weight is critical to obtain nature-like or structural tailor cut glycosaminoglycan homologues. However, so far, it has been scarcely investigated. In this paper, for the first time, a new protocol was set up to determine the molecular weights of the capsular polysaccharides of three wild-type and three engineered E. coli K5 and K4 strains. The protocol includes a small-scale downstream train to purify the intact polysaccharides, directly from the fermentation broth supernatants, by using ultrafiltration membranes and anion exchange chromatography, and it couples size exclusion chromatography analyses with triple detector array. In the purification high recovery (> 85.0%) and the removal of the main contaminant, the lipopolysaccharide, were obtained. The averaged molecular weights of the wild-type capsular polysaccharides ranged from 51.3 to 90.9 kDa, while the engineered strains produced polysaccharides with higher molecular weights, ranging from 68.4 to 130.6 kDa, but with similar polydispersity values between 1.1 and 1.5.
肝素和硫酸软骨素分别用作抗血栓和抗骨关节炎药物,但它们的药理作用取决于其结构特征,如硫酸化程度和分子量。近年来,新的基于发酵的生物技术方法试图从大肠杆菌 K5 和 K4 产生的肝素聚糖和类似软骨素荚膜多糖开始获得肝素和硫酸软骨素。研究微生物荚膜多糖的分子量对于获得天然或结构定制的糖胺聚糖类似物至关重要。然而,到目前为止,这方面的研究还很少。本文首次建立了一种新的方案,用于确定三种野生型和三种工程化大肠杆菌 K5 和 K4 菌株的荚膜多糖的分子量。该方案包括一个小规模的下游处理流程,用于通过超滤膜和阴离子交换色谱直接从发酵液上清液中纯化完整的多糖,并将尺寸排阻色谱分析与三重检测器阵列相结合。在纯化过程中,回收率高(>85.0%),并去除了主要污染物,即脂多糖。野生型荚膜多糖的平均分子量范围为 51.3 至 90.9 kDa,而工程菌株产生的多糖分子量更高,范围为 68.4 至 130.6 kDa,但多分散性值在 1.1 至 1.5 之间相似。