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首页> 外文期刊>Applied Microbiology and Biotechnology >The atf2 gene is involved in triacylglycerol biosynthesis and accumulation in the oleaginous Rhodococcus opacus PD630
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The atf2 gene is involved in triacylglycerol biosynthesis and accumulation in the oleaginous Rhodococcus opacus PD630

机译:atf2基因参与三酰基甘油的生物合成和在油性不透明红球菌PD630中的积累

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摘要

Rhodococcus opacus PD630 is an oleaginous bacterium able to accumulate large amounts of triacylglycerols (TAG) in different carbon sources. The last reaction for TAG biosynthesis is catalyzed by the bifunctional wax ester synthase/acyl-CoA:diacylglycerol acyltransferase (WS/DGAT) enzymes encoded by atf genes. R. opacus PD630 possesses at least 17 putative atf homologous genes in its genome, but only atf1 and atf2 exhibited a significant DGAT activity when expressed in E. coli, as revealed in a previous study. The contribution of atf1 gene to TAG accumulation by strain PD630 has been demonstrated previously, although additional Atfs may also contribute to lipid accumulation, since the atf1-disrupted mutant is still able to produce significant amounts of TAG (Alvarez et al., Microbiology 154:2327-2335, 2008). In this study, we investigated the in vivo role of atf2 gene in TAG accumulation by R. opacus PD630 by using different genetic strategies. The atf2-disrupted mutant exhibited a decrease in TAG accumulation (up to 25-30 %, w/w) and an approximately tenfold increase in glycogen formation in comparison with the wild-type strain. Surprisingly, in contrast to single mutants, a double mutant generated by the disruption of atf1 and atf2 genes only showed a very low effect in TAG and in glycogen accumulation under lipid storage conditions. Overexpression of atf1 and atf2 genes in strain PD630 promoted an increase of approximately 10 % (w/w) in TAG accumulation, while heterologous expression of atf2 gene in Mycobacterium smegmatis caused an increase in TAG accumulation during cultivation in nitrogen-rich media. This study demonstrated that, in addition to atf1 gene, atf2 is actively involved in TAG accumulation by the oleaginous R. opacus PD630.
机译:不透明红球菌PD630是一种油脂性细菌,能够在不同的碳源中积累大量的三酰甘油(TAG)。 TAG生物合成的最后反应是由atf基因编码的双功能蜡酯合酶/酰基-CoA:二酰基甘油酰基转移酶(WS / DGAT)酶催化的。如先前的研究所揭示的那样,欧波罗氏菌PD630在其基因组中至少具有17个推定的atf同源基因,但是只有atf1和atf2在大肠杆菌中表达时才显示出显着的DGAT活性。先前已经证明了atf1基因对PD630菌株对TAG积累的贡献,尽管额外的Atfs也可能对脂质积累有贡献,因为atf1突变的突变体仍然能够产生大量的TAG(Alvarez等人,Microbiology 154: 2327-2335,2008)。在这项研究中,我们调查了atf2基因在体内的作用,通过使用不同的遗传策略,由不透明芽孢杆菌PD630进行TAG积累。与野生型菌株相比,受atf2干扰的突变体表现出TAG积累减少(最多25-30%,w​​ / w),糖原形成增加约十倍。出乎意料的是,与单突变体相反,由atf1和atf2基因的破坏产生的双突变体在脂类储存条件下对TAG和糖原积累的作用极低。 PD630菌株中atf1和atf2基因的过表达促进TAG积累增加约10%(w / w),而耻垢分枝杆菌中atf2基因的异源表达导致在富氮培养基中培养期间TAG积累增加。这项研究表明,除了atf1基因外,atf2还通过油性乳球菌PD630积极参与TAG的积累。

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