Pourzardosht Navid, Rasaee Mohammad Javad
Department of Clinical Biochemistry, School of Medical Sciences, Tarbiat Modares University, Chamran -Jalal Crossing, P.O. Box 14115-331, Tehran, Iran.
Mol Biotechnol. 2017 Jun;59(6):192-199. doi: 10.1007/s12033-017-0005-z.
Despite the significant potential of Streptococcus zooepidemicus for hyaluronic acid (HA) production with high molecular weight (MW), the HA degrading properties of hyaluronidase prevents the bacteria to achieve enhanced HA yield with high MW. In the present study, we aim to knockout the hyaluronidase enzyme and assess its effects on the yield and MW of the produced HA. The kanamycin resistance gene between the left and right arms of hyaluronidase gene was inserted into pUC18 plasmid to construct pUC18-L-kana-R as a recombinant suicide plasmid. The construct was then transferred into S. zooepidemicus to induce the homologous recombination between the hyaluronidase gene and the kanamycin resistance gene. Gene deletion was confirmed by PCR and enzyme assay. The product was cultured on selectable medium in which the MW of HA was increased from 1.5 to 3.8 MDa. The yield of HA production using the mutant strain was higher in all different concentrations of glucose from 40 to 120 g/l. Moreover, glucose increase results in higher HA production within both wild-type and recombinant strains. However, the growth rate of HA concentration (the slope of the plot), as a consequence of increased glucose concentration, is always higher for the recombinant strain. Unlike the wild-type strain, there was no sharp HA production drop approaching the 6 g/l HA concentration. In conclusion, hyaluronidase activity and HA concentration and MW exhibited a mutual control on each other. Based on our results, deletion of the hyaluronidase gene positively affects the yield and MW of HA.
尽管兽疫链球菌在生产高分子量透明质酸(HA)方面具有巨大潜力,但透明质酸酶对HA的降解特性阻碍了该细菌实现高分子量HA产量的提高。在本研究中,我们旨在敲除透明质酸酶,并评估其对所产生HA的产量和分子量的影响。将透明质酸酶基因左臂和右臂之间的卡那霉素抗性基因插入pUC18质粒,构建重组自杀质粒pUC18-L-kana-R。然后将构建体转入兽疫链球菌,诱导透明质酸酶基因与卡那霉素抗性基因之间的同源重组。通过PCR和酶活性测定确认基因缺失。将产物在选择培养基上培养,其中HA的分子量从1.5 MDa增加到3.8 MDa。在40至120 g/l的所有不同葡萄糖浓度下,使用突变菌株生产HA的产量都更高。此外,葡萄糖浓度增加会导致野生型菌株和重组菌株的HA产量均升高。然而,由于葡萄糖浓度增加,重组菌株的HA浓度增长速率(曲线斜率)始终更高。与野生型菌株不同,在接近6 g/l HA浓度时,HA产量没有急剧下降。总之,透明质酸酶活性与HA浓度和分子量之间存在相互调控关系。基于我们的结果,敲除透明质酸酶基因对HA的产量和分子量有积极影响。