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Titlebook: Genetic Transformation Systems in Fungi, Volume 2; Marco A. van den Berg,Karunakaran Maruthachalam Book 2015 Springer International Publis

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樓主: Chylomicron
11#
發(fā)表于 2025-3-23 10:25:26 | 只看該作者
Arginase (,) as a Fungal Transformation Markerto grow on .-arginine as the sole nitrogen source. Transforming such a strain with an . expression construct allows it to utilize .-arginine. The .. recipient host along with an . expression construct describes arginase as a conditional nutritional marker. A protocol to use this arginine selection f
12#
發(fā)表于 2025-3-23 14:19:49 | 只看該作者
Transformation of Ascomycetous Fungi Using Autonomously Replicating Vectorstors containing the AMA1 sequence derived from . have been used to increase transformation efficiency, improve expression of target genes, and facilitate construction of genomic libraries, suggesting that AMA1-bearing vectors may be applicable to a wide range of fungal species. Here we describe a tr
13#
發(fā)表于 2025-3-23 20:01:19 | 只看該作者
14#
發(fā)表于 2025-3-24 01:52:13 | 只看該作者
Split-Marker-Mediated Transformation and Targeted Gene Disruption in Filamentous Fungibeen shown to increase homologous integration and thereby, facilitate targeted gene disruption in many fungi. Because the selectable marker gene is truncated in different fragments, the gene is not functional until homologous recombination takes place between two overlapping fragments. The truncated
15#
發(fā)表于 2025-3-24 03:51:33 | 只看該作者
16#
發(fā)表于 2025-3-24 08:43:56 | 只看該作者
Diffusive Mass Transfer by Solution,le-genome sequences became available for fungi, it became possible to predict the repeat content of a whole genome and calculate RIP mutation across a large number of sequences from multiple repeat families. The software tool RIPCAL was developed for this purpose and since its release has become widely used in fungal genome analysis pipelines.
17#
發(fā)表于 2025-3-24 12:11:04 | 只看該作者
18#
發(fā)表于 2025-3-24 15:30:51 | 只看該作者
Helmut Münstedt,Friedrich Rudolf Schwarzlone repair via homologous recombination. Here we describe detailed protocols for implementing TaGTEAM in yeast, suitability of the technique for various evolutionary engineering goals, and considerations for porting TaGTEAM to other fungal species and beyond.
19#
發(fā)表于 2025-3-24 19:43:24 | 只看該作者
https://doi.org/10.1007/978-94-011-1896-5efold compared with a genome-integrating vector. The AMA1 vectors were maintained extrachromosomally in most transformants. In addition, co-transformation using multiple AMA1-bearing vectors was also successful. AMA1-bearing vectors are a useful addition to the experimental toolbox for many transformation experiments.
20#
發(fā)表于 2025-3-25 00:55:18 | 只看該作者
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