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A novel plasmid addiction system for large-scale production of cyanophycin in Escherichia coli using mineral salts medium

机译:利用矿物盐培养基在大肠杆菌中大规模生产蓝霉素的新型质粒成瘾系统

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Introduction: Hitherto the production of the biopolymer cyanophycin (CGP) using recombinant Escherichia coli strains and cheap mineral salts medium yielded only trace amounts of CGP (<0.5%, w/w) of the cell dry matter (CDM). This was probably due to the instability of the plasmids encoding the cyanophycin synthetase. Material and methods: In this study, we developed an anabolism-based media-dependent plasmid addiction system (PAS) to enhance plasmid stability, and we established a process based on a modified mineral salts medium yielding a CGP content of 42% (w/w) at the maximum without the addition of amino acids to the medium for the first time. This PAS is based on different lysine biosynthesis pathways and consists of two components: (1) a knockout of the chromosomal dapE disrupts the native succinylase pathway in E. coli and (2) the complementation by the plasmid-encoded artificial aminotransferase pathway mediated by the dapL gene from Synechocystis sp. PCC 6308, which allows the synthesis of the essential lysine precursor L,L-2,6-diaminopimelate. In addition, this plasmid also harbors cphAC595S, an engineered cyanophycin synthetase gene responsible for CGP production. Results: Cultivation experiments in Erlenmeyer flask and also in bioreactors in mineral salts medium without antibiotics revealed an at least 4.5-fold enhanced production of CGP in comparison to control cultivations without PAS. Discussion: Fermentation experiments with culture volume of up to 400 l yielded a maximum of 18% CGP (w/w) and a final cell density of 15.2 g CDM/l. Lactose was used constantly as an effective inducer and carbon source. Thus, we present a convenient option to produce CGP with E. coli at a technical scale without the need to add antibiotics or amino acids using the mineral salts medium designed in this study.
机译:简介:迄今为止,使用重组大肠杆菌菌株和廉价的无机盐培养基生产生物聚合物蓝藻素(CGP)只能产生痕量的细胞干物质(CDM)CGP(<0.5%,w / w)。这可能是由于编码蓝霉素合成酶的质粒不稳定。材料和方法:在这项研究中,我们开发了一种基于合成代谢的依赖于培养基的质粒成瘾系统(PAS),以增强质粒的稳定性,并且我们建立了一种基于改良的矿物盐培养基的工艺,该工艺的CGP含量为42%(w / w)第一次不向培养基中添加氨基酸的最大值。该PAS基于不同的赖氨酸生物合成途径,并且由两个部分组成:(1)敲除染色体dapE破坏了大肠杆菌中的天然琥珀酸酶途径,(2)由质粒编码的人工转氨酶途径介导的互补作用。来自集胞藻的dapL基因。 PCC 6308,可合成必需的赖氨酸前体L,L-2,6-二氨基庚二酸酯。此外,该质粒还带有cphAC595S,cphAC595S是负责CGP产生的工程化蓝藻合成酶基因。结果:在锥形瓶中以及在没有抗生素的无机盐培养基中的生物反应器中的培养实验表明,与没有PAS的对照培养相比,CGP的产量提高了至少4.5倍。讨论:培养体积最大为400 l的发酵实验产生的最大CGP(w / w)为18%,最终细胞密度为15.2 g CDM / l。乳糖一直被用作有效的诱导剂和碳源。因此,我们提出了一种方便的选择,可以用技术规模的大肠杆菌生产CGP,而无需使用本研究设计的无机盐培养基添加抗生素或氨基酸。

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