Suppr超能文献

[关于在不同碳源及培养基中不同氧气浓度下生长的酿酒酵母中无机多磷酸盐含量的研究]

[Study of the content of inorganic polyphosphates in Saccharomyces cerevisiae grown on different carbon sources with different O2 concentrations in the medium].

作者信息

Vagabov V M, Trilisenko L V, Kulakovskaia E V, Kulaev I S

出版信息

Mikrobiologiia. 2008 Sep-Oct;77(5):611-6.

Abstract

The content of different fractions of inorganic polyphosphates (polyP) was studied in Saccharomyces cerevisiae VKM Y-1173 growing on a complete medium with glucose under hypoxia and active aeration as well as on ethanol. The highest growth rate was observed for aerobic fermentation, while the yield of biomass was maximal for cultivation on ethanol. In the mid-log growth phase, the amount of polyP was maximal in the cells grown on glucose under hypoxia and minimal on ethanol. In this latter case, the content of different polyP fractions changed unevenly: polyP3, polyP4, and polyP1 decreased by approximately 60%, 45%, and 30%, respectively; the salt-soluble polyP2 remained at almost the same level; while polyP5 abruptly increased 10- to 15-fold. These findings demonstrate that the metabolic pathways for polyP fractions are different. A significant drop in the amount of the main polyP fractions accompanied by a decrease of the polyP average chain length in the presence of carbon and Pi sources in the medium is evidence of active involvement of polyP as additional energy sources in the flows of energy in actively growing yeast cells.

摘要

研究了酿酒酵母VKM Y - 1173在含葡萄糖的完全培养基上于缺氧、通气良好条件下以及在乙醇上生长时不同无机多聚磷酸盐(polyP)组分的含量。需氧发酵时观察到最高生长速率,而在乙醇上培养时生物量产量最大。在对数生长中期,缺氧条件下在葡萄糖上生长的细胞中多聚磷酸盐的量最大,在乙醇上生长的细胞中多聚磷酸盐的量最小。在后一种情况下,不同多聚磷酸盐组分的含量变化不均匀:多聚磷酸盐3(polyP3)、多聚磷酸盐4(polyP4)和多聚磷酸盐1(polyP1)分别减少约60%、45%和30%;盐溶性多聚磷酸盐2(polyP2)几乎保持在相同水平;而多聚磷酸盐5(polyP5)突然增加10至15倍。这些发现表明多聚磷酸盐组分的代谢途径不同。在培养基中存在碳源和磷源的情况下,主要多聚磷酸盐组分的量显著下降,同时多聚磷酸盐平均链长减小,这证明多聚磷酸盐作为额外能量来源积极参与活跃生长的酵母细胞的能量流动。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验