Addition of the appropriate restriction enzyme to linearized transforming DNA has been shown to increase transformation efficiencies in organisms as diverse as Saccharomyces cerevisiae (Schiestl and Petes 1991 Proc. Nat. Acad. Sci. USA 88:7585-7589) and Dictyostelium discoideum (Kuspa and Loomis 1992 Proc. Nat. Acad. Sci. USA 89:8803- 8807). This process has been described as REMI, for restriction enzyme-mediated integration. We have examined the effect of restriction enzyme addition on transformation efficiencies in Neurospora crassa. The frequency of cotransformation of a qa-2 inl double mutant with two plasmids [one containing the selectable marker qa-2+ (quinate utilization) and the other containing inl+ (inositol)] was also examined, a...
When a gene or an unidentified fragment of DNA from an organism has been cloned, it is often useful...
We report the complementation of the Neurospora crassa pyr-4 mutation with the Aspergillus nidulans ...
The qa-2+ gene has been widely used as a selectable marker in Neurospora transformations (Akins and ...
Cloning structural and regulatory genes of Neurospora and their manipulation in vitro will allow...
When a gene or other fragment of DNA is cloned. it is often useful to identify the chrom...
A rapid and efficient approach for Neurospora crassa transformation using low melting point agarose ...
The presence of restriction enzymes in the transformation mixture improved the efficiency of transfo...
The quinic acid inducible qa-2 promoter of Neurospora crassa has been used to express cloned genes b...
Abstract only availableIn order to maintain genomic integrity, organisms must possess the capability...
Difference between transformed and spontaneous revertant strains of Neurospora crass
Transformation of N. crassa using the calcium chloride/polyethylene glycol procedure (Fincham 1989. ...
For targeted gene disruption in wild-type Neurospora crassa, 1000-bp of homologous sequences on eith...
In filamentous fungi transformed with linear DNA, the frequency of gene replacement varies from a fe...
Plasmids based on the cloned inositol gene of Neurospora crassa are potentially very useful as a tra...
Characterization in inl+ transformants of Neurospora crassa obtained with a recombinant cosmid-poo
When a gene or an unidentified fragment of DNA from an organism has been cloned, it is often useful...
We report the complementation of the Neurospora crassa pyr-4 mutation with the Aspergillus nidulans ...
The qa-2+ gene has been widely used as a selectable marker in Neurospora transformations (Akins and ...
Cloning structural and regulatory genes of Neurospora and their manipulation in vitro will allow...
When a gene or other fragment of DNA is cloned. it is often useful to identify the chrom...
A rapid and efficient approach for Neurospora crassa transformation using low melting point agarose ...
The presence of restriction enzymes in the transformation mixture improved the efficiency of transfo...
The quinic acid inducible qa-2 promoter of Neurospora crassa has been used to express cloned genes b...
Abstract only availableIn order to maintain genomic integrity, organisms must possess the capability...
Difference between transformed and spontaneous revertant strains of Neurospora crass
Transformation of N. crassa using the calcium chloride/polyethylene glycol procedure (Fincham 1989. ...
For targeted gene disruption in wild-type Neurospora crassa, 1000-bp of homologous sequences on eith...
In filamentous fungi transformed with linear DNA, the frequency of gene replacement varies from a fe...
Plasmids based on the cloned inositol gene of Neurospora crassa are potentially very useful as a tra...
Characterization in inl+ transformants of Neurospora crassa obtained with a recombinant cosmid-poo
When a gene or an unidentified fragment of DNA from an organism has been cloned, it is often useful...
We report the complementation of the Neurospora crassa pyr-4 mutation with the Aspergillus nidulans ...
The qa-2+ gene has been widely used as a selectable marker in Neurospora transformations (Akins and ...