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Transfer of the high GC cyclohexane carboxylate degradation pathway from Rhodopseudomonas palustris to Escherichia coli for production of biotin

机译:将高GC环己烷羧酸盐降解途径从古红假单胞菌转移至大肠杆菌以生产生物素

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摘要

This work demonstrates the transfer of the five gene cyclohexane carboxylate (CHC) degradation pathway from the high GC alphaproteobacterium Rhodopseudomonas palustris to Escherichia coli, a gammaproteobacterium. The degradation product of this pathway is pimeloyl-CoA, a key metabolite in E. coli's biotin biosynthetic pathway. This pathway is useful for biotin overproduction in E. coli, however, the expression of GC-rich genes is troublesome in this host. When the native R. palustris CHC degradation pathway is transferred to a ΔbioH pimeloyl-CoA auxotroph of E. coli, it is unable to complement growth in the presence of CHC. To overcome this expression problem we redesigned the operon with decreased GC content and removed stretches of high GC intergenic DNA which comprise the 5' untranslated region of each gene, replacing these features with shorter low GC sequences. We show this synthetic construct enables growth of the ΔbioH strain in the presence of CHC. When the synthetic degradation pathway is overexpressed in conjunction with the downstream genes for biotin biosynthesis, we measured significant accumulation of biotin in the growth medium, showing that the pathway transfer is successfully integrated with the host metabolism.
机译:这项工作证明了五个基因环己烷羧酸盐(CHC)降解途径从高GCα变形杆菌Rhodopseudomonas palustris转移到大肠杆菌,一种γ变形杆菌。该途径的降解产物是庚二酰辅酶A,这是大肠杆菌生物素生物合成途径中的关键代谢产物。该途径对于大肠杆菌中生物素的过量生产是有用的,但是,富含GC的基因的表达在该宿主中是麻烦的。当天然帕氏疟原虫CHC降解途径转移至大肠杆菌的ΔbioH庚二酰辅酶A营养缺陷型时,它无法在存在CHC时补充生长。为克服此表达问题,我们重新设计了具有降低的GC含量的操纵子,并去除了包含每个基因5'非翻译区的高GC基因间DNA片段,并用较短的低GC序列代替了这些特征。我们证明了这种合成构建体能够在CHC存在下使ΔbioH菌株生长。当合成降解途径与生物素生物合成的下游基因一起过表达时,我们测量了生物素在生长培养基中的大量积累,表明途径转移已成功与宿主代谢整合。

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