Suppr超能文献

用于设计嗜腺嘌呤阿氏酵母表达载体的多形汉逊酵母和嗜腺嘌呤阿氏酵母来源的rDNA靶向元件的评估。

Assessment of Hansenula polymorpha and Arxula adeninivorans-derived rDNA-targeting elements for the design of Arxula adeninivorans expression vectors.

作者信息

Steinborn Gerhard, Gellissen Gerd, Kunze Gotthard

机构信息

Institut für Pflanzengenetik und Kulturpflanzenforschung, Corrensstr. 3, D-06466 Gatersleben, Germany.

出版信息

FEMS Yeast Res. 2005 Nov;5(11):1047-54. doi: 10.1016/j.femsyr.2005.07.005. Epub 2005 Aug 24.

Abstract

Different targeting sequences derived from the Arxula adeninivorans and Hansenula polymorpha rDNA clusters were tested in A. adeninivorans integration/expression vectors. For element identification, the rDNA unit of A. adeninivorans (accession number ) was first isolated and characterized in addition to the known H. polymorpha unit. The rDNA is a cluster of some forty 7653-bp units without the 5S rDNA gene. The selected elements were integrated into a set of A. adeninivorans expression/integration vectors harbouring a TEF1 promoter - amyA ORF - PHO5 terminator sequence as reporter gene. No differences in mitotic stability, copy number and transformation frequency were observed. All transformants harboured a single copy integrated into the rDNA by a homologous recombination. In contrast, the choice of the rDNA targeting sequence was found to be of impact on productivity. Use of ETS-18S-5.8S fragments from both organisms resulted in a more than 50% increase in comparison to the use of other elements, independent of the orientation within the vector.

摘要

在嗜腺嘌呤丛赤壳菌整合/表达载体中测试了源自嗜腺嘌呤丛赤壳菌和多形汉逊酵母rDNA簇的不同靶向序列。为了进行元件鉴定,除了已知的多形汉逊酵母rDNA单元外,还首先分离并鉴定了嗜腺嘌呤丛赤壳菌的rDNA单元(登录号 )。该rDNA是由约四十个7653 bp单元组成的簇,不含5S rDNA基因。将选定的元件整合到一组含有TEF1启动子-amyA开放阅读框-PHO5终止子序列作为报告基因的嗜腺嘌呤丛赤壳菌表达/整合载体中。未观察到有丝分裂稳定性、拷贝数和转化频率的差异。所有转化体都通过同源重组在rDNA中整合了一个单拷贝。相比之下,发现rDNA靶向序列的选择对生产力有影响。与使用其他元件相比,使用来自这两种生物的ETS-18S-5.8S片段可使产量提高50%以上,且与载体中的方向无关。

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