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作 者:张春艳[1] 丁庆豹[2] 许彦梅 魏晓琨 欧伶[2] 张鹭[1]
机构地区:[1]齐齐哈尔大学生命科学与工程学院,黑龙江齐齐哈尔161006 [2]华东理工大学生物反应器工程重点实验室,上海200237 [3]上海璞诚生物科技有限公司,上海200235
出 处:《中国热带医学》2009年第2期241-243,共3页China Tropical Medicine
基 金:国家科技部科技型中小企业技术创新基金(07C26213101283)
摘 要:目的选育胞苷脱氨酶缺失枯草芽孢杆菌,提高胞苷发酵单位,并对间歇补料分批发酵方式进行了初步研究。方法(1)以胞苷脱氨酶缺失枯草芽孢杆菌CDS36为突发菌株,对其进行紫外诱变,经6-杂氮尿嘧啶(6AU)、5-氟胞苷(5FCR)等进行定向抗性筛选;(2)采用间歇补料分批发酵,葡萄糖初始浓度10.0%,48h后补加10.0%,72h补加5.0%的补料方式培养,并测定发酵单位。结果(1)通过紫外诱变和抗性筛选得到了6-杂氮尿嘧啶、5-氟胞苷抗性的突变株CDS36-800-17,抗6-杂氮尿嘧啶和5-氟胞苷的临界浓度分别为1000mg/L和800mg/L;(2)通过间歇补料分批发酵方式发现培养96h,胞苷发酵单位可达4.86g/L,培养120h可达5.58g/L,比未经补料分批发酵时提高了20.0%。结论(1)筛选获得胞苷发酵单位较高的突变株CDS36-800-17,并具有较好的遗传稳定性,可稳定发酵;(2)间歇补料分批发酵方式可提高胞苷产量。Objective To derive a mutant which can increase the yield of cytidine from Bacillus subtilis which deficient in eytidine deaminase and observe the process of eytidine production of intermittent fed-batch fermentation. Methods ( 1 ) Inducing Bacillus subtilis CDS36 (deficient in eytidine deaminase) by ultraviolet, the mutant was selected directionally and stepwisely on the agar plates containing 6AU and 5FCR. (2)Intermittent fed-batch fermentation: 10% glucose was fed 48 hours later and 5% glucose was fed again 72 hours later, when the initial glucose concentration was 10%, the yield of cytidine was detected . Results (1)a mutant Bacillus subtilis CDS36-800-17 resisatnat to 6AU and 5FCR was otained. The critical resistance concentrations of 6AU and 5FCR were 1000mg/L and 800mg/L ,respectively; 2)The yield of eytidine was 5.58g/L and that of eytidine was 4.86g/L 96 and 120 hours after fermentation, Cytidine production was increased 20% through feed fermentation than through batch fermentation. Conclusion Cytidine overproducing mutant, Bacillus subtilis CDS36-800-17 with stable heredity and fermentation has been obtained,.Intermittent fed-batch fermentation methods can enhance the yoel of cytidine.
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