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High Polyhydroxybutyrate Production in Pseudomonas extremaustralis Is Associated with Differential Expression of Horizontally Acquired and Core Genome Polyhydroxyalkanoate Synthase Genes

机译:极端假单胞菌中的高聚羟基丁酸酯生产与水平获得和核心基因组聚羟基链烷酸合酶基因的差异表达有关。

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摘要

Pseudomonas extremaustralis produces mainly polyhydroxybutyrate (PHB), a short chain length polyhydroxyalkanoate (sclPHA) infrequently found in Pseudomonas species. Previous studies with this strain demonstrated that PHB genes are located in a genomic island. In this work, the analysis of the genome of P. extremaustralis revealed the presence of another PHB cluster phbFPX, with high similarity to genes belonging to Burkholderiales, and also a cluster, phaC1ZC2D, coding for medium chain length PHA production (mclPHA). All mclPHA genes showed high similarity to genes from Pseudomonas species and interestingly, this cluster also showed a natural insertion of seven ORFs not related to mclPHA metabolism. Besides PHB, P. extremaustralis is able to produce mclPHA although in minor amounts. Complementation analysis demonstrated that both mclPHA synthases, PhaC1 and PhaC2, were functional. RT-qPCR analysis showed different levels of expression for the PHB synthase, phbC, and the mclPHA synthases. The expression level of phbC, was significantly higher than the obtained for phaC1 and phaC2, in late exponential phase cultures. The analysis of the proteins bound to the PHA granules showed the presence of PhbC and PhaC1, whilst PhaC2 could not be detected. In addition, two phasin like proteins (PhbP and PhaI) associated with the production of scl and mcl PHAs, respectively, were detected. The results of this work show the high efficiency of a foreign gene (phbC) in comparison with the mclPHA core genome genes (phaC1 and phaC2) indicating that the ability of P. extremaustralis to produce high amounts of PHB could be explained by the different expression levels of the genes encoding the scl and mcl PHA synthases.
机译:极端假单胞菌主要产生多羟基丁酸酯(PHB),一种短链长度的多羟基链烷酸酯(sclPHA),很少见于假单胞菌物种。先前对该菌株的研究表明,PHB基因位于基因岛中。在这项工作中,对极端疟原虫基因组的分析表明存在另一个PHB簇phbFPX,该簇与Burkholderiales的基因高度相似,还有一个簇phaC1ZC2D,编码中等链长PHA产生(mclPHA)。所有mclPHA基因均显示与假单胞菌属物种的基因高度相似,有趣的是,该簇也显示了与mclPHA代谢无关的七个ORF的自然插入。除了PHB,极少量的P. extremaustralis还能产生mclPHA。互补分析表明,mclPHA合成酶PhaC1和PhaC2均具有功能。 RT-qPCR分析显示PHB合酶,phbC和mclPHA合酶的表达水平不同。在后期指数期培养中,phbC的表达水平明显高于phaC1和phaC2。对与PHA颗粒结合的蛋白质的分析表明,存在PhbC和PhaC1,而无法检测到PhaC2。此外,还检测到了两种分别与scl和mcl PHAs产生相关的类似phasin的蛋白(PhbP和PhaI)。这项工作的结果表明,与mclPHA核心基因组基因(phaC1和phaC2)相比,外源基因(phbC)的效率高,这表明极端表达假单胞菌产生大量PHB的能力可以通过不同的表达来解释。 scl和mcl PHA合成酶的基因水平。

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