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吐温40和DtsR1对钝齿棒杆菌中L-精氨酸过量生产的影响。

Effect of Tween 40 and DtsR1 on L-arginine overproduction in Corynebacterium crenatum.

作者信息

Chen Minliang, Chen Xuelan, Wan Fang, Zhang Bin, Chen Jincong, Xiong Yonghua

机构信息

College of Life Science, Nanchang University, Nanchang, 330031, People's Republic of China.

State Key Laboratory of Food Science and Technology, Jiangxi-OAI Joint Research Institute, Nanchang University, 235 Nanjing East Road, Nanchang, 330047, People's Republic of China.

出版信息

Microb Cell Fact. 2015 Aug 12;14:119. doi: 10.1186/s12934-015-0310-9.

Abstract

BACKGROUND

L-Glutamate is an important precursor in the L-arginine (L-Arg) biosynthetic pathway. Various methods, including polyoxyethylene sorbitan monopalmitate (Tween 40) addition and dtsR1 disruption, have been widely used to induce L-glutamate overproduction in Corynebacterium glutamicum. In this study, a novel strategy for L-Arg overproduction through Tween 40 trigger and ΔdtsR1 mutant were proposed in Corynebacterium crenatum.

RESULTS

Corynebacterium crenatum mutant (CCM01) was selected as a host strain, whose argR was lethal via mutagenesis screening, the proB gene was knocked out, and argB was replaced by argB M4 (E19R, H26E, D311R, and D312R) to release L-Arg feedback resistance. After Tween 40 trigger in the logarithmic period, L-Arg production increased from 15.22 to 17.73 g/L in CCM01 strain. When NCgl1221 and dtsR1 disruption (CCM03), L-Arg production drastically increased to 27.45 g/L and then further to 29.97 g/L after Tween 40 trigger. Moreover, the specific activity of α-oxoglutarate dehydrogenase complex (ODHC) decreased, whereas the regeneration of NADP(+)/NADPH significantly increased after dtsR1 disruption and Tween 40 trigger. Results of real-time PCR showed that the transcriptional levels of odhA, sucB, and lpdA (encoding three subunits of the ODHC complex) were downregulated after Tween 40 trigger or dtsR1 disruption. By contrast, zwf transcription (encoding glucose-6-phosphate dehydrogenase) showed no significant difference among CCM01, CCM02 (ΔNCgl1221), and CCM03 (ΔNCgl1221ΔdtsR1) strains without Tween 40 trigger but evidently increased by 5.50 folds after Tween 40 trigger.

CONCLUSION

A novel strategy for L-Arg overproduction by dtsR1 disruption and Tween 40 trigger in C. crenatum was reported. Tween 40 addition exhibited a bifunctional mechanism for L-Arg overproduction, including reduced ODHC activity and enhanced NADPH pools accumulation by downregulated dtsR1 expression and upregulated zwf expression, respectively.

摘要

背景

L-谷氨酸是L-精氨酸(L-Arg)生物合成途径中的重要前体。包括添加聚氧乙烯山梨醇酐单棕榈酸酯(吐温40)和破坏dtsR1在内的各种方法已被广泛用于诱导谷氨酸棒杆菌过量生产L-谷氨酸。在本研究中,提出了一种通过吐温40触发和ΔdtsR1突变体在圆红冬孢酵母中过量生产L-精氨酸的新策略。

结果

选择圆红冬孢酵母突变体(CCM01)作为宿主菌株,通过诱变筛选使其argR致死,敲除proB基因,并用argB M4(E19R、H26E、D311R和D312R)取代argB以解除L-精氨酸的反馈抗性。在对数期用吐温40触发后,CCM01菌株中的L-精氨酸产量从15.22 g/L增加到17.73 g/L。当破坏NCgl1221和dtsR1(CCM03)时,L-精氨酸产量急剧增加至27.45 g/L,在吐温40触发后进一步增加至29.97 g/L。此外,α-酮戊二酸脱氢酶复合体(ODHC)的比活性降低,而在破坏dtsR1和吐温40触发后,NADP(+)/NADPH的再生显著增加。实时PCR结果表明,在吐温40触发或破坏dtsR1后,odhA、sucB和lpdA(编码ODHC复合体的三个亚基)的转录水平下调。相比之下,在没有吐温40触发的CCM01、CCM02(ΔNCgl1221)和CCM03(ΔNCgl1221ΔdtsR1)菌株中,zwf转录(编码葡萄糖-6-磷酸脱氢酶)没有显著差异,但在吐温40触发后明显增加了5.50倍。

结论

报道了一种通过破坏dtsR1和吐温40触发在圆红冬孢酵母中过量生产L-精氨酸的新策略。添加吐温40对L-精氨酸过量生产具有双功能机制,包括分别通过下调dtsR1表达和上调zwf表达来降低ODHC活性和增强NADPH池积累。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0cc/4534012/bb3b774206af/12934_2015_310_Fig1_HTML.jpg

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