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Comparison of Different Strategies to Reduce Acetate Formation in Escherichia coli

机译:减少大肠杆菌中乙酸形成的不同策略的比较

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E.coli cells produce acetate as an extracellular coproduct of aerobic cultures.Acetate is undesirable because it retards growth and inhibits protein formation.Most process designs or genetic modifications to minimize acetate formation aim at balancing growth rate and oxygen consumption.In this research,three genetic approaches to reduce acetate formation were investigated:(1)direct reduction of the carbon flow to acetate(ackA-pta,poxB knock-out);(2)anticipation on the underlying metabolic and regulatory mechanisms that lead to acetate(constitutive ppc expression mutant);and(3)both(1)and(2).Initially,these mutants were compared to the wild-type E.coli via batch cultures under aerobic conditions.Subsequently,these mutants were further characterized using metabolic flux analysis on continuous cultures.It is concluded that a combination of directly reducing the carbon flow to acetate and anticipating on the underlying metabolic and regulatory mechanism that lead to acetate,is the most promising approach to overcome acetate formation and improve recombinant protein production.These genetic modifications have no significant influence on the metabolism when growing the microorganisms under steady state at relatively low dilution rates(less than 0.4 h~(-1)).
机译:大肠杆菌细胞产生的乙酸盐是有氧培养的细胞外副产物。乙酸盐是不可取的,因为它阻碍了生长并抑制了蛋白质的形成。大多数工艺设计或基因改造可最大程度地减少乙酸盐的形成,目的是平衡生长速率和耗氧量。研究了减少乙酸盐生成的遗传方法:(1)直接减少碳流向乙酸盐的转化(ackA-pta,poxB敲除);(2)预期导致乙酸盐的潜在代谢和调控机制(组成性ppc表达)首先,通过在有氧条件下通过分批培养将这些突变体与野生型大肠杆菌进行比较。随后,使用连续连续代谢通量分析对这些突变体进行进一步表征结论是最直接的途径是直接减少碳流向乙酸盐的流向并预测导致乙酸盐的潜在代谢和调节机制。这些基因修饰对微生物以相对较低的稀释率(小于0.4 h〜(-1))在稳态下生长时的代谢没有显着影响。

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