Borovikova Diana, Rozenfelde Linda, Pavlovska Ilona, Rapoport Alexander
Laboratory of Cell Biology, Institute of Microbiology and Biotechnology, University of Latvia, Kronvald blvd., 4, Riga LV-1586, Latvia.
Laboratory of Cell Biology, Institute of Microbiology and Biotechnology, University of Latvia, Kronvald blvd., 4, Riga LV-1586, Latvia.
J Biotechnol. 2014 Aug 20;184:169-71. doi: 10.1016/j.jbiotec.2014.05.017. Epub 2014 Jun 2.
This study was performed with the goal of revealing if the dehydration procedure used in our new immobilisation method noticeably decreases the viability of yeast cells in immobilised preparations. Various yeasts were used in this research: Saccharomyces cerevisiae cells that were rather sensitive to dehydration and had been aerobically grown in an ethanol-containing medium, a recombinant strain of S. cerevisiae grown in aerobic conditions which were completely non-resistant to dehydration and an anaerobically grown bakers' yeast strain S. cerevisiae, as well as a fairly resistant Pichia pastoris strain. Experiments performed showed that immobilisation of all these strains essentially increased their resistance to a dehydration-rehydration treatment. The increase of cells' viability (compared with control cells dehydrated in similar conditions) was from 30 to 60%. It is concluded that a new immobilisation method, which includes a dehydration stage, does not lead to an essential loss of yeast cell viability. Correspondingly, there is no risk of losing the biotechnological activities of immobilised preparations. The possibility of producing dry, active yeast preparations is shown, for those strains that are very sensitive to dehydration and which can be used in biotechnology in an immobilised form. Finally, the immobilisation approach can be used for the development of efficient methods for the storage of recombinant yeast strains.
本研究旨在揭示我们新的固定化方法中使用的脱水程序是否会显著降低固定化制剂中酵母细胞的活力。本研究使用了多种酵母:对脱水相当敏感且在含乙醇培养基中好氧生长的酿酒酵母细胞、在好氧条件下生长且完全不耐脱水的酿酒酵母重组菌株、厌氧生长的面包酵母菌株酿酒酵母,以及相当耐脱水的毕赤酵母菌株。所进行的实验表明,所有这些菌株的固定化基本上提高了它们对脱水 - 再水化处理的抗性。细胞活力的增加(与在类似条件下脱水的对照细胞相比)为30%至60%。得出的结论是,包括脱水阶段的新固定化方法不会导致酵母细胞活力的显著损失。相应地,固定化制剂不会有丧失生物技术活性的风险。对于那些对脱水非常敏感且可固定化形式用于生物技术的菌株,展示了生产干燥、活性酵母制剂的可能性。最后,固定化方法可用于开发重组酵母菌株的高效储存方法。