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Studies on the production of branched-chain alcohols in engineered Ralstonia eutropha

机译:工程化Ralstonia eutropha中支链醇生产的研究

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摘要

Wild-type Ralstonia eutropha H16 produces polyhydroxybutyrate (PHB) as an intracellular carbon storage material during nutrient stress in the presence of excess carbon. In this study, the excess carbon was redirected in engineered strains from PHB storage to the production of isobutanol and 3-methyl-1-butanol (branched-chain higher alcohols). These branched-chain higher alcohols can directly substitute for fossil-based fuels and be employed within the current infrastructure. Various mutant strains of R. eutropha with isobutyraldehyde dehydrogenase activity, in combination with the overexpression of plasmid-borne, native branched-chain amino acid biosynthesis pathway genes and the overexpression of heterologous ketoisovalerate decarboxylase gene, were employed for the biosynthesis of isobutanol and 3-methyl-1-butanol. Production of these branched-chain alcohols was initiated during nitrogen or phosphorus limitation in the engineered R. eutropha. One mutant strain not only produced over 180 mg/L branched-chain alcohols in flask culture, but also was significantly more tolerant of isobutanol toxicity than wild-type R. eutropha. After the elimination of genes encoding three potential carbon sinks (ilvE, bkdAB, and aceE), the production titer improved to 270 mg/L isobutanol and 40 mg/L 3-methyl-1-butanol. Semicontinuous flask cultivation was utilized to minimize the toxicity caused by isobutanol while supplying cells with sufficient nutrients. Under this semicontinuous flask cultivation, the R. eutropha mutant grew and produced more than 14 g/L branched-chain alcohols over the duration of 50 days. These results demonstrate that R. eutropha carbon flux can be redirected from PHB to branched-chain alcohols and that engineered R. eutropha can be cultivated over prolonged periods of time for product biosynthesis.
机译:在存在过量碳的情况下,在营养胁迫期间,野生型富营养的Ralstonia eutropha H16产生多羟基丁酸酯(PHB)作为细胞内碳存储材料。在这项研究中,过量的碳在工程菌株中从PHB储存重定向到异丁醇和3-甲基-1-丁醇(支链高级醇)的生产。这些支链高级醇可直接替代基于化石的燃料,并在当前基础设施中使用。具有异丁醛脱氢酶活性的富营养富营养芽孢杆菌的各种突变菌株,与质粒携带的天然支链氨基酸生物合成途径基因的过表达和异源酮异戊酸脱羧酶基因的过表达相结合,用于异丁醇和3-的生物合成。甲基-1-丁醇。在工程化富营养红球菌的氮或磷限制期间,开始生产这些支链醇。一株突变菌株不仅在烧瓶培养中产生了超过180 mg / L的支链醇,而且比野生型富营养红杆菌对异丁醇毒性的耐受性要强得多。消除编码三个潜在碳汇的基因(ilvE,bkdAB和aceE)后,生产效价提高到270 mg / L异丁醇和40 mg / L 3-甲基-1-丁醇。利用半连续烧瓶培养来最小化由异丁醇引起的毒性,同时为细胞提供足够的营养。在这种半连续烧瓶培养条件下,富营养R. eutropha突变体在50天内持续生长并产生了超过14 g / L的支链醇。这些结果表明,富营养的R.碳通量可以从PHB重定向到支链醇,工程化的富营养的R.富营养化可以长时间培养以用于产物的生物合成。

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