首页> 外文期刊>Bioresource Technology: Biomass, Bioenergy, Biowastes, Conversion Technologies, Biotransformations, Production Technologies >Enhanced production of medium-chain-length polyhydroxyalkanoates (PHA) by PHA depolymerase knockout mutant of Pseudomonas putida KT2442
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Enhanced production of medium-chain-length polyhydroxyalkanoates (PHA) by PHA depolymerase knockout mutant of Pseudomonas putida KT2442

机译:恶臭假单胞菌KT2442的PHA解聚酶敲除突变体提高了中链长度的多羟基链烷酸酯(PHA)的产量

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摘要

Pseudomonas putida KT2442 is a medium-chain-length polyhydroxyalkanoates (PHA) producer. One of the main shortages in the production Of PHA has been the intracellular PHA degradation caused by its endogenous PHA depolymerase. The aim of this study was to improve PHA production via removing the PHA degradation mechanism. PHA depolymerase phaZ knockout mutant A putida KTMQ01 was successfully constructed, which accumulated 86 wt% medium-chain-length PHA (mcl PHA) when cultured in mineral medium containing sodium octanoate as the carbon source compared with P. putida KT2442 which produced only 66 wt% of its cell dry weight (CDW). P. putida KTMQ01 cultured over a five-day period on sodium octanoate produced 4.5 g L (1) - 4.0 g L (1) CDW containing approximately 80 wt% PHA without degradation. In contrast, A putida KT2442 was observed with decreasing CDW and PHA from over 4 to less than 2 g L-1 over the same period of time. indicating the function of PHA depolymerases which reduced the amount of PHA from around 50 wt% to none over the incubation period. RT-PCR analysis showed that phaC2 transcriptional level of A putida KTMQ01 was higher than that of P. putida KT2442, indicating the possibility of relief on negative control of phaC2 transcription by the deletion of phaZ, which combined with the lack of in vivo PHA degradation, led to more PHA accumulation. A putida KTMQ01 contained PHA granules with larger sizes and smaller numbers than those of A putida KT2442.
机译:恶臭假单胞菌KT2442是中链长度的聚羟基链烷酸酯(PHA)生产商。生产PHA的主要不足之一是由其内源PHA解聚酶引起的细胞内PHA降解。这项研究的目的是通过消除PHA降解机理来提高PHA的产量。 PHA解聚酶phaZ敲除突变体A成功构建了putida KTMQ01,与仅产生66 wt%的恶臭假单胞菌KT2442相比,在含有辛酸钠作为碳源的矿物培养基中培养时,该菌积累了86 wt%的中链长度PHA(mcl PHA)。细胞干重的百分比(CDW)。在辛酸钠上培养五天的恶臭假单胞菌KTMQ01产生了4.5 g L(1)-4.0 g L(1)CDW,其中含有约80 wt%的PHA而没有降解。相比之下,观察到恶臭KT2442的CDW和PHA在同一时间段内从超过4 g L-1降至少于2 g L-1。表明PHA解聚酶的功能使PHA的量在孵育期间从约50wt%降低至无。 RT-PCR分析表明,恶臭假单胞菌KTMQ01的phaC2转录水平高于恶臭假单胞菌KT2442,表明通过删除phaZ可以缓解对phaC2转录负控制的可能性,并缺乏体内PHA的降解。 ,导致更多的PHA积累。 Putida KTMQ01包含的PHA颗粒比A Putida KT2442具有更大的尺寸和更少的数量。

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