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双功能尿苷酰转移/去除酶GlnD在谷氨酸棒杆菌JNR中的功能 被引量:2
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作者 李静 徐美娟 +6 位作者 舒群峰 赵雅雯 唐蜜 张显 杨套伟 许正宏 饶志明 《微生物学报》 CAS CSCD 北大核心 2019年第11期2206-2217,共12页
【目的】通过改造谷氨酸棒杆菌JNR中双功能尿苷酰转移/去除酶GlnD,减弱尿苷酰去除酶的活性,增强NH4+的转运和利用,提高L-精氨酸的合成。【方法】本文对来源于谷氨酸棒杆菌的突变菌株JNR中的双功能尿苷酰转移/去除酶GlnD进行整合突变,采... 【目的】通过改造谷氨酸棒杆菌JNR中双功能尿苷酰转移/去除酶GlnD,减弱尿苷酰去除酶的活性,增强NH4+的转运和利用,提高L-精氨酸的合成。【方法】本文对来源于谷氨酸棒杆菌的突变菌株JNR中的双功能尿苷酰转移/去除酶GlnD进行整合突变,采用同源重组的方法将H414和D415位点突变为两个丙氨酸AA,在此菌株的基础上过量表达PII蛋白GlnK,并对其进行尿苷酰化研究,离子色谱检测摇瓶发酵过程中NH4+的浓度,并对最终的改造菌株进行连续流加发酵分析。【结果】该双功能尿苷酰转移/去除酶在谷氨酸棒杆菌中成功进行整合突变,有效减弱了尿苷酰去除酶的活性;同时过表达PII蛋白GlnK,其酰基化程度明显增强。摇瓶发酵结果表明菌株L4消耗NH4+增加,L-精氨酸产量为36.2±1.2 g/L,比对照菌株L3高出22.7%。5-L发酵罐实验结果显示改造菌株L4的L-精氨酸的产量为52.2 g/L,较野生型菌株L0提高了25.3%。【结论】谷氨酸棒杆菌合成L-精氨酸的过程中氮源是必不可少的。减弱GlnD尿苷酰去除酶的活性后,胞内尿苷酰化的GlnK-UMP增加,GlnK-UMP与氮转录调控因子AmtR结合,转运至胞内的NH4+浓度提高,促使L-精氨酸产量显著提高。 展开更多
关键词 谷氨酸棒杆菌JNR 双功能尿苷酰转移/去除酶GlnD NH4+ L-精氨酸 整合突变
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离子转运蛋白调控钝齿棒杆菌离子和pH稳态促进L-精氨酸合成 被引量:1
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作者 刘晶 徐美娟 +5 位作者 满在伟 高惠芳 张显 杨套伟 许正宏 饶志明 《微生物学报》 CAS CSCD 北大核心 2020年第10期2277-2291,共15页
L-精氨酸是一种半必需氨基酸,广泛应用于食品、制药、饲料等行业。【目的】当前对L-精氨酸生产菌株的研究,极少涉及离子转运领域。在本研究中,发现在发酵时适量添加外源K+有利于促进钝齿棒杆菌(Corynebacterium crenatum)SYPA5-5合成L-... L-精氨酸是一种半必需氨基酸,广泛应用于食品、制药、饲料等行业。【目的】当前对L-精氨酸生产菌株的研究,极少涉及离子转运领域。在本研究中,发现在发酵时适量添加外源K+有利于促进钝齿棒杆菌(Corynebacterium crenatum)SYPA5-5合成L-精氨酸。【方法】在C.crenatum SYPA5-5发酵培养基外源添加0.5 g/L和2.5 g/L的K3PO4,取对数期发酵样品进行转录组数据分析,挖掘出K+转运相关的阳离子转运ATP酶CTAP1以及单价阳离子/H+逆转运蛋白Mrp1A,研究其在C.crenatum SYPA5-5快速合成L-精氨酸阶段,对菌株生长及L-精氨酸合成的影响。【结果】对基因ctap1和mrp1分别进行敲除和过表达,深入研究突变株对L-精氨酸合成的影响。研究发现同时过表达离子转运蛋白CTAP1和Mrp1A更有利于胞内离子、pH稳态和渗透压调节,最终提高L-精氨酸的产量。在补料分批发酵中分别过表达Mrp1A、CTAP1以及同时过表达Mrp1A和CTAP1的菌株L-精氨酸产量分别达到61.4 g/L、63.9 g/L和65.3 g/L,产率分别为0.383 g/g、0.392 g/g和0.395 g/g,比C.crenatum SYPA5-5分别提高了34.9%、38.0%和39.1%。【结论】CTAP1是特异性的K+转运ATP酶,可以将培养基中的K+运输到胞内。同时Mrp1A可将胞内K+和Na+等单价阳离子运输到胞外,将胞外H+运输至胞内,中和胞内L-精氨酸所导致的碱性环境,从而维持胞内pH稳定。CTAP1和Mrp1A的研究为解析离子转运机制和L-精氨酸合成之间的联系奠定了基础。 展开更多
关键词 钝齿棒杆菌SYPA5-5 阳离子转运ATP酶CTAP1 单价阳离子/H+逆转运蛋白Mrp1A 钾离子
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Sequence and thermodynamic characteristics of terminators revealed by FlowSeq and the discrimination of terminators strength
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作者 Weiji Zhai Yanting Duan +5 位作者 Xiaomei Zhang Guoqiang xu Hui Li Jinsong Shi zhenghong xu Xiaojuan Zhang 《Synthetic and Systems Biotechnology》 SCIE 2022年第4期1046-1055,共10页
The intrinsic terminator in prokaryotic forms secondary RNA structure and terminates the transcription.However,leaking transcription is common due to varied terminator strength.Besides of the representative hairpin an... The intrinsic terminator in prokaryotic forms secondary RNA structure and terminates the transcription.However,leaking transcription is common due to varied terminator strength.Besides of the representative hairpin and U-tract structure,detailed sequence and thermodynamic features of terminators were not completely clear,and the effect of terminator on the upstream gene expression was unclearly.Thus,it is still challenging to use terminator to control expression with higher precision.Here,in E.Coli,we firstly determined the effect of the 3′-end sequences including spacer sequences and terminator sequences on the expression of upstream and downstream genes.Secondly,terminator mutation library was constructed,and the thermodynamic and sequence features differing in the termination efficiency were analyzed using the FlowSeq technique.The result showed that under the regulation of terminators,a negative correlation was presented between the expression of upstream and downstream genes(r=0.60),and the terminators with lower free energy corelated with higher upstream gene expression.Meanwhile,the terminator with longer stem length,more compact loop and perfect U-tract structure was benefit to the transcription termination.Finally,a terminator strength classification model was established,and the verification experiment based on 20 synthetic terminators indicated that the model can distinguish strong and weak terminators to certain extent.The results help to elucidate the role of terminators in gene expression,and the key factors identified are crucial for rational design of terminators,and the model provided a method for terminator strength prediction. 展开更多
关键词 Intrinsic terminator Transcription termination Machine learning Structure-activity relationship FlowSeq Free energy
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Characterization and implications of prokaryotic ribosome-binding sites across species
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作者 Yanting Duan Xiaojuan Zhang +6 位作者 Weiji Zhai Jinpeng Zhang Jiawei Ren Xiaomei Zhang Guoqiang xu Jinsong Shi zhenghong xu 《Systems Microbiology and Biomanufacturing》 2022年第4期676-684,共9页
The ribosome-binding site(RBS)in the 5′untranslated region is recognized by 16S rRNA to start translation and is an essential element of the gene expression system.RBSs have been widely applied in regulating gene exp... The ribosome-binding site(RBS)in the 5′untranslated region is recognized by 16S rRNA to start translation and is an essential element of the gene expression system.RBSs have been widely applied in regulating gene expression in various scenarios,including Gram-negative or Gram-positive bacteria.Here,we first rationally designed and constructed an RBS mutant library containing 66 RBSs.The strength of these RBSs in E.coli and C.glutamicum was characterized individually.The RBS strength spanned about 200 and 15 times in the two species,respectively.The strength of RBSs in C.glutamicum was generally lower than that of in E.coli.A total of 18 RBSs showed similar strength(within twofold differences)between the species in our study,and the correlation analysis of the strength of RBSs between E.coli and C.glutamicum(R^(2)=0.7483)revealed that these RBSs can be used across species.The sequence analysis revealed that the RBS region with two Ts stated was beneficial for RBS to function cross-species.The RBS characterized here can be used to precisely regulate gene expression in both hosts,and the characteristics of cross-species RBSs provide basic information for RBS rational design. 展开更多
关键词 RBS library Cross-species RBSs Sequence characteristics Escherichia coli Corynebacterium glutamicum
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