Mueller Dirk, Stahl Ulf, Meyer Vera
Technische Universität Berlin, Institut für Biotechnologie, Fachgebiet Mikrobiologie und Genetik, Germany.
J Microbiol Methods. 2006 Jun;65(3):585-95. doi: 10.1016/j.mimet.2005.10.003. Epub 2005 Nov 18.
Metabolic engineering in filamentous fungi is a emerging field of research as many fungi produce high value primary and secondary metabolites. Ribozyme technology can be used as a tool for metabolic engineering to influence metabolic pathways and to knock down the expression of specific genes of interest. Hammerhead ribozymes can target virtually any mRNA sequence of choice and prevent gene expression on the post-transcriptional level. They are thus a versatile tool for timed and spatial elimination of unwanted gene products. As current research has only investigated the application of ribozymes in bacteria, yeast and mammalian cells, we decided to carry out a study on whether this technology can also function with filamentous fungi. We employed a sensitive, quantitative reporter-based model system as a proof of concept, using the Escherichia coli beta-glucuronidase transcript (uidA) as the target mRNA and Aspergillus giganteus as the host. This system was used to validate the in vivo activities of seven different hammerhead ribozymes, which were selected by in silico analysis of the uidA mRNA. All ribozymes tested were able to reduce the reporter activity up to a maximum of 100%, demonstrating that ribozyme technology is indeed a useful tool in fungal metabolic engineering.
由于许多真菌能产生高价值的初级和次级代谢产物,丝状真菌的代谢工程是一个新兴的研究领域。核酶技术可作为代谢工程的一种工具,用于影响代谢途径并敲低特定目标基因的表达。锤头状核酶几乎可以靶向任何选定的mRNA序列,并在转录后水平上阻止基因表达。因此,它们是用于在时间和空间上消除不需要的基因产物的通用工具。由于目前的研究仅调查了核酶在细菌、酵母和哺乳动物细胞中的应用,我们决定开展一项研究,探究该技术在丝状真菌中是否也能发挥作用。我们采用了一个基于敏感定量报告基因的模型系统作为概念验证,以大肠杆菌β-葡萄糖醛酸酶转录本(uidA)作为目标mRNA,以巨大曲霉作为宿主。该系统用于验证通过对uidA mRNA进行计算机分析选择的七种不同锤头状核酶的体内活性。所有测试的核酶都能够将报告基因活性降低高达100%,这表明核酶技术在真菌代谢工程中确实是一种有用的工具。