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首页> 外文期刊>Applied biochemistry and biotechnology, Part A. enzyme engineering and biotechnology >Development of an Agrobacterium-Mediated Transformation Method and Evaluation of Two Exogenous Constitutive Promoters in Oleaginous Yeast Lipomyces starkeyi
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Development of an Agrobacterium-Mediated Transformation Method and Evaluation of Two Exogenous Constitutive Promoters in Oleaginous Yeast Lipomyces starkeyi

机译:农杆菌介导的转化方法的发展及两种外源构成促进剂的转化方法及其评价含有植物酵母脂质症

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摘要

Oleaginous yeast Lipomyces starkeyi, a promising strain of great biotechnical importance, is able to accumulate over 60% of its cell biomass as triacylglycerols (TAGs). It is promising to directly produce the derivatives of TAGs, such as long-chain fatty acid methyl esters and alkanes, in L. starkeyi. However, techniques for genetic modification of this oleaginous yeast are lacking, thus, further research is needed to develop genetic tools and functional elements. Here, we used two exogenous promoters (pGPD and pPGK) from oleaginous yeast Rhodosporidium toruloides to establish a simpler Agrobacterium-mediated transformation (AMT) method for L. starkeyi. Hygromycin-resistant transformants were obtained on antibiotic-contained plate. Mitotic stability test, genotype verification by PCR, and protein expression confirmation all demonstrated the success of this method. Furthermore, the strength of these two promoters was evaluated at the phenotypic level on a hygromycin-gradient plate and at the transcriptional level by real-time quantitative PCR. The PGK promoter strength was 2.2-fold as that of GPD promoter to initiate the expression of the hygromycin-resistance gene. This study provided an easy and efficient genetic manipulation method and elements of the oleaginous yeast L. starkeyi for constructing superior strains to produce advanced biofuels.
机译:Olafigilous酵母Lipomyces Starkeyi,具有巨大的生物技术重要性,能够积聚超过60%的细胞生物质作为三酰基甘油(标签)。有希望直接产生标签的衍生物,如长链脂肪酸甲酯和烷烃,在L. StarKeyi中。然而,缺乏这种含油酵母的遗传修饰的技术缺乏,因此需要进一步研究来开发遗传工具和功能元件。在这里,我们使用来自Olabilicous酵母紫红素孢子座的两个外源启动子(PGPD和PPGK),以建立L. StarKeyi的更简单的农杆菌介导的转化(AMT)方法。在抗生素含有板上得到耐霉素的转化体。有丝分裂稳定性试验,通过PCR进行基因型验证,蛋白表达确认都证明了该方法的成功。此外,通过实时定量PCR在对潮霉素梯度板上的表型水平和转录水平上评价这两个启动子的强度。 PGK启动子强度作为GPD启动子的促进剂强度为2.2倍,以引发潮霉素抗性基因的表达。本研究提供了一种易于高效的遗传操作方法和烯胺酵母L. StarKeyi的元素,用于构建优质菌株以生产先进的生物燃料。

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