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2型猪链球菌细胞分裂蛋白DivIVA的原核表达及纯化 被引量:3
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作者 倪华 过雨晴 +6 位作者 杜世仁 张剑 范伟伟 孙卫平 王长军 曹祥荣 潘秀珍 《中国病原生物学杂志》 CSCD 北大核心 2016年第6期500-504,508,共6页
目的利用原核表达系统制备2型猪链球菌细胞分裂起始因子DivIVA重组蛋白并进行纯化,为研究其在调控细胞分裂中的作用奠定基础。方法以2型猪链球菌05ZYH33全基因组为模板,PCR扩增divIVA基因片段,经BamHⅠ和XholⅠ双酶切后将目的片段连接... 目的利用原核表达系统制备2型猪链球菌细胞分裂起始因子DivIVA重组蛋白并进行纯化,为研究其在调控细胞分裂中的作用奠定基础。方法以2型猪链球菌05ZYH33全基因组为模板,PCR扩增divIVA基因片段,经BamHⅠ和XholⅠ双酶切后将目的片段连接至表达载体pET28a,构建重组表达质粒pET28a-divIVA,经测序鉴定后将重组质粒转化进入表达菌E.coli BL21,以终浓度为0.1mmol/L的IPTG于37℃培养4h,诱导DivIVA蛋白表达。用Ni离子亲和层析柱分离纯化目的蛋白,SDS-PAGE和Western blot进行检测和验证。结果成功构建重组表达质粒pET28a-divIVA,并在E.coli BL21中表达主要以包涵体形式存在的DivIVA蛋白。包涵体蛋白经8mol/L脲变性溶解后经Ni离子亲和层析柱纯化,获得的目的蛋白经SDS-PAGE检测分子质量为36ku,与预期大小相符;经Western blot检测,该蛋白能被相应抗体特异性识别。结论在E.coli BL21中成功表达并纯化了DivIVA蛋白,为研究该蛋白在2型猪链球菌的细胞分裂机制奠定了基础。 展开更多
关键词 2型猪链球菌 diviva蛋白 蛋白原核表达
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Enhancing single-cell hyaluronic acid biosynthesis by microbial morphology engineering 被引量:4
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作者 Yukun Zheng Fangyu Cheng +1 位作者 Bo Zheng Huimin Yu 《Synthetic and Systems Biotechnology》 SCIE 2020年第4期316-323,共8页
Microbial morphology engineering is a novel approach for cell factory to improve the titer of target product in bio-manufacture.Hyaluronic acid(HA),a valuable glycosaminoglycan polymerized by HA synthase(HAS),a membra... Microbial morphology engineering is a novel approach for cell factory to improve the titer of target product in bio-manufacture.Hyaluronic acid(HA),a valuable glycosaminoglycan polymerized by HA synthase(HAS),a membrane protein,is particularly selected as the model product to improve its single-cell HA-producing capacity via morphology engineering.DivIVA and FtsZ,the cell-elongation and cell division related protein,respectively,were both down/up dual regulated in C.glutamicum via weak promoter substitution or plasmid overexpression.Different from the natural short-rod shape,varied morphologies of engineered cells,i.e.small-ellipsoid-like(DivIVA-reduced),bulb-like(DivIVA-enhanced),long-rod(FtsZ-reduced)and dumbbell-like(FtsZ-enhanced),were observed.Applying these morphology-changed cells as hosts for HA production,the reduced expression of both DivIVA and FtsZ seriously inhibited normal cell growth;meanwhile,overexpression of DivIVA didn't show morphology changes,but overexpression of FtsZ surprisingly change the cell-shape into long and thick rod with remarkably enlarged single-cell surface area(more than 5.2-fold-increase).And finally,the single-cell HA-producing capacity of the FtsZ-overexpressed C.glutamicum was immensely improved by 13.5-folds.Flow cytometry analyses verified that the single-cell HAS amount on membrane was enhanced by 2.1 folds.This work is pretty valuable for high titer synthesis of diverse metabolic products with microbial cell factory. 展开更多
关键词 Morphology engineering Single-cell HA-Producing capacity diviva protein FtsZ protein Down/up dual regulation Enlarged cells
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