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分批补料培养过程中大肠杆菌膜结构与功能的表征

Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation.

作者信息

Shokri Atefeh, Larsson Gen

机构信息

The Swedish Centre for Bioprocess Technology, Albanova University Centre, KTH SE-106 91 Stockholm, SWEDEN.

出版信息

Microb Cell Fact. 2004 Jul 28;3(1):9. doi: 10.1186/1475-2859-3-9.

Abstract

BACKGROUND

Important parameters during recombinant protein production in Escherichia coli, such as productivity and protein activity, are affected by the growth rate. This includes the translocation of protein over the membrane to gain better folding capacity or reduced proteolysis. To vary the growth rate two techniques are available: fedbatch and continuous cultivation, both controlled by the ingoing feed rate. RESULTS: During fedbatch cultivation, E. coli contains phosphatidylethanolamine, phosphatidylglycerol, cardiolipin and saturated fatty acids in amounts which are stable with growth rate. However, the levels of cardiolipin are very high compared to continuous cultivation. The reason for fedbatch triggering of this metabolism is not known but hypothesised to result from an additional need for carbon and energy. The reason could be the dynamic and sometimes rapid changes in growth rate to which the fedbatch cell has at all times to adjust. The membrane flexibility, essential for translocation of various components, is however to some degree sustained by production of increased amounts of unsaturated fatty acids in phosphatidylglycerol. The result is a functionally stiff membrane which generally promotes low cell lysis and is constant with respect to protein leakage to the medium. At comparatively high growth rates, when the further stabilising effect of cyclic fatty acids is gone, the high level of unsaturated fatty acids results in a pronounced effect upon sonication. This is very much in contrast to the membrane function in continuous cultivation which shows very specific characteristics as a function of growth rate. CONCLUSIONS: The stiff and unchanging fedbatch membrane should promote a stable behaviour during downstream processing and is less dependent on the time of harvest. However, optimisation of protein leakage can only be achieved in the continuously cultivated cell where leakage is twice as high compared to the constant leakage level in fedbatch. If leakage is undesired, continuous cultivation is also preferred since it can be designed to lead to the lowest values detected. Induction at low growth rate (<0.2 h-1) should be avoided with respect to productivity, in any system, since the specific and total protein production shows their lowest values at this point.

摘要

背景

在大肠杆菌中生产重组蛋白时,诸如生产率和蛋白活性等重要参数会受到生长速率的影响。这包括蛋白质跨膜转运以获得更好的折叠能力或减少蛋白水解。为了改变生长速率,有两种技术可供选择:补料分批培养和连续培养,两者均由进料速率控制。

结果

在补料分批培养过程中,大肠杆菌中磷脂酰乙醇胺、磷脂酰甘油、心磷脂和饱和脂肪酸的含量随生长速率保持稳定。然而,与连续培养相比,心磷脂的水平非常高。补料分批培养引发这种代谢的原因尚不清楚,但据推测是由于对碳和能量的额外需求。原因可能是补料分批培养的细胞始终需要适应生长速率的动态变化,有时这种变化还很快。然而,对于各种成分的转运至关重要的膜柔韧性,在一定程度上通过磷脂酰甘油中不饱和脂肪酸产量的增加得以维持。结果是形成了一种功能上僵硬的膜,这种膜通常能促进较低的细胞裂解率,并且在蛋白质泄漏到培养基方面保持恒定。在相对较高的生长速率下,当环状脂肪酸的进一步稳定作用消失时,高水平的不饱和脂肪酸会对超声处理产生显著影响。这与连续培养中的膜功能形成了鲜明对比,连续培养中的膜功能表现出非常特定的生长速率依赖性特征。

结论

僵硬且不变的补料分批培养膜应能在下游加工过程中促进稳定的行为,并且对收获时间的依赖性较小。然而,只有在连续培养的细胞中才能实现蛋白质泄漏的优化,因为连续培养细胞中的泄漏率是补料分批培养中恒定泄漏水平的两倍。如果不希望出现泄漏,连续培养也是首选,因为它可以设计成导致检测到的最低值。就生产率而言,在任何系统中,都应避免在低生长速率(<0.2 h-1)下诱导,因为此时比蛋白产量和总蛋白产量均处于最低值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4096/514524/d11cd851e7a8/1475-2859-3-9-1.jpg

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