Suppr超能文献

产油丝状真菌高山被孢霉1S-4整体转化体系的建立

Establishment of an overall transformation system for an oil-producing filamentous fungus, Mortierella alpina 1S-4.

作者信息

Takeno Seiki, Sakuradani Eiji, Murata Shoichi, Inohara-Ochiai Misa, Kawashima Hiroshi, Ashikari Toshihiko, Shimizu Sakayu

机构信息

Laboratory of Fermentation Physiology and Applied Microbiology, Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University, 606-8502, Kyoto, Japan.

出版信息

Appl Microbiol Biotechnol. 2004 Sep;65(4):419-25. doi: 10.1007/s00253-004-1622-6. Epub 2004 May 12.

Abstract

Oil-producing fungus Mortierella alpina 1S-4 is an industrial strain. To determine its physiological properties and to clarify the biosynthetic pathways for polyunsaturated fatty acids, a transformation system for this fungus was established using a derivative of it, i.e., a ura5- mutant lacking orotate phosphoribosyl transferase (OPRTase, EC.2.4.2.10) activity. Transformation with a vector containing the homologous ura5 gene as a marker was successfully performed using microprojectile bombardment, other methods frequently used for transformation, such as the protoplasting, lithium acetate, or electroporation methods, not giving satisfactory results. As a result, two types of transformants were obtained: a few stable transformants overexpressing the ura5 gene, and many unstable transformants showing OPRTase activity comparable to that of the wild-type strain. The results of quantitative PCR indicated that the stable transformants could retain the ura5 genes originating from the transformation vector regardless of the culture conditions. On the other hand, unstable transformants easily lost the marker gene under uracil-containing conditions, as expected. In this paper, we report that an overall transformation system for this fungus was successfully established, and propose how to select useful transformants as experimental and industrial strains.

摘要

产油真菌高山被孢霉1S-4是一种工业菌株。为了确定其生理特性并阐明多不饱和脂肪酸的生物合成途径,利用该真菌的一个衍生物,即缺乏乳清酸磷酸核糖基转移酶(OPRTase,EC.2.4.2.10)活性的ura5-突变体,建立了该真菌的转化系统。使用微粒轰击成功地进行了以含有同源ura5基因作为标记的载体的转化,而其他常用于转化的方法,如原生质体法、醋酸锂法或电穿孔法,均未得到满意的结果。结果,获得了两种类型的转化体:少数过表达ura5基因的稳定转化体,以及许多显示出与野生型菌株相当的OPRTase活性的不稳定转化体。定量PCR结果表明,无论培养条件如何,稳定转化体都能保留来自转化载体的ura5基因。另一方面,正如预期的那样,不稳定转化体在含尿嘧啶的条件下很容易丢失标记基因。在本文中,我们报告成功建立了该真菌的整体转化系统,并提出了如何选择有用的转化体作为实验菌株和工业菌株。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验