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首页> 外文期刊>Journal of Genetic Engineering and Biotechnology >Phylogenetic analysis of isolated biofuel yeasts based on 5.8S-ITS rDNA and D1/D2 26S rDNA sequences
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Phylogenetic analysis of isolated biofuel yeasts based on 5.8S-ITS rDNA and D1/D2 26S rDNA sequences

机译:基于5.8S-ITS rDNA和D1 / D2 26S rDNA序列的分离的生物燃料酵母的系统发育分析

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The utilization of agro-industrial wastes such as whey as raw materials for the production of bio-ethanol is gaining importance as a result of the attractiveness of renewable fuel alternatives due to exhaustion of fossil fuel sources coupled with the positive impact to the environment. Here, we report the isolation of two Kluyveromyces spp. designated as BM4 and P41, able to produce ethanol as main fermentation product from fermenting whey. Three different molecular biological approaches including, the RFLP analysis of the 5.8S-ITS rDNA, the sequence of the 5.8S-ITS rDNA region and the sequence of the D1/D2 domain of the 26S rRNA gene were applied for accurate identification. While RFLP analysis of 5.8S-ITS region failed to accurate the differentiation between the two species, sequencing of this region and D1/D2 region of the 26S rRNA gene verified the identification. PCR amplification and sequence analysis of 5.8S-ITS rRNA and D1/D2 domain of the 26S rRNA genes revealed that the isolates BM4 and P41 were highly related to Kluyveromyces marxianus and Kluyveromyces lactis with homology of 99% for both. In addition, phylogenetic analysis indicated that both BM4 and P41 shared a cluster with K. marxianus and K. lactis, respectively. The fermentative performance of both strains on cheese whey to produce ethanol was evaluated at different parameters such as incubation temperature, initial pH, whey sugar concentrations, and yeast concentrations. Results show that the maximum ethanol productions achieved at pH 4.5 and 35^oC were 5.52% and 5.05% for K. marxianus and K. lactis, respectively. Our results demonstrated that K. marxianus and K. Lactis could be recommended for cheese whey bioremediation in the environment and produce renewable biofuel.
机译:由于用尽化石燃料源以及对环境的积极影响,可再生燃料替代品具有吸引力,因此将乳清等农业工业废物用作生产生物乙醇的重要性日益提高。在这里,我们报告了两个克鲁维酵母属物种的分离。命名为BM4和P41,能够从发酵乳清中产生乙醇作为主要发酵产物。 5.8S-ITS rDNA的RFLP分析,5.8S-ITS rDNA区域的序列和26S rRNA基因的D1 / D2结构域的序列这三种不同的分子生物学方法可用于准确鉴定。尽管对5.8S-ITS区的RFLP分析无法准确区分两个物种,但对该区域和26S rRNA基因的D1 / D2区进行测序验证了这一识别。 26S rRNA基因的5.8S-ITS rRNA和D1 / D2结构域的PCR扩增和序列分析表明,分离株BM4和P41与马克斯克鲁维酵母和乳酸克鲁维酵母高度相关,两者的同源性为99%。此外,系统发育分析表明,BM4和P41分别与马克斯克鲁维酵母和乳酸克鲁维酵母共享一个簇。在不同的参数下,如温育温度,初始pH,乳清糖浓度和酵母浓度,评估了两种菌株在干酪乳清上产生乙醇的发酵性能。结果表明,在pH 4.5和35℃下,马克斯克鲁维酵母和乳酸克鲁维酵母的最大乙醇产量分别为5.52%和5.05%。我们的结果表明,K。marxianus和K. Lactis可推荐用于环境中的干酪乳清生物修复并生产可再生生物燃料。

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