Abstract
BspLUII III, an isomer of FinI (1) and BsmFI (2), was found to cleave DNA at two points 10, 11 and 14, 15 bp in the different strands away from the recognition site, and in the presence of SAM it exhibits the adenine specific methyltransferase activity.
Full text
PDF

Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brown N. L., Smith M. A general method for defining restriction enzyme cleavage and recognition sites. Methods Enzymol. 1980;65(1):391–404. doi: 10.1016/s0076-6879(80)65050-2. [DOI] [PubMed] [Google Scholar]
- Heusterspreute M., Davison J. Restriction site bank vectors. II. DNA sequence analysis of plasmid pJRD158. DNA. 1984 Jun;3(3):259–268. doi: 10.1089/dna.1.1984.3.259. [DOI] [PubMed] [Google Scholar]
- Janulaitis A., Petrusyte M., Maneliene Z., Klimasauskas S., Butkus V. Purification and properties of the Eco57I restriction endonuclease and methylase--prototypes of a new class (type IV). Nucleic Acids Res. 1992 Nov 25;20(22):6043–6049. doi: 10.1093/nar/20.22.6043. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kessler C., Manta V. Specificity of restriction endonucleases and DNA modification methyltransferases a review (Edition 3). Gene. 1990 Aug 16;92(1-2):1–248. doi: 10.1016/0378-1119(90)90486-b. [DOI] [PubMed] [Google Scholar]