| Application | Comment | Organism |
|---|---|---|
| molecular biology | DNA recombination methods employ commerciually available DNA methyltransferase expression vectors, that protect selected sites on different plasmids from particular Type II restriction endonucleases. One methods employs 4 restriction endonuclease and 2 methyltransferases in a discontinuous DNA assembly and produces more desired recombinant plasmids and produces fewer undesired recombination products as conventional subcloning. The 5 restriction endonucleases/methyltransferases continuous DNA assembly is approximately as efficient and specific as conventional Golden Gate assembly, even though in vivo methylation of one plasmid is incomplete | Escherichia coli |
| molecular biology | DNA recombination methods employ commercially available DNA methyltransferase expression vectors, that protect selected sites on different plasmids from particular Type II restriction endonucleases. One method employs 4 restriction endonuclease and 2 methyltransferases in a discontinuous DNA assembly and produces more desired recombinant plasmids and produces fewer undesired recombination products as conventional subcloning. The 5 restriction endonucleases/methyltransferases continuous DNA assembly is approximately as efficient and specific as conventional Golden Gate assembly, even though in vivo methylation of one plasmid is incomplete | Streptomyces spectabilis |
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Escherichia coli | P00642 | isoform EcoRI | - |
| Streptomyces spectabilis | A8WEY4 | isoform SpeI | - |