Induction of Various Mutations during PCRs with Manganese and 8-Hydroxy-dGTP
To induce various mutations randomly, PCRs with Mn2+ and with a mutagenic deoxyribonucleotide, 8-hydroxy-dGTP (8-OH-dGTP), were performed. Mutations were induced by deoxyribonucleotide imbalance plus 500 μM Mn2+ in the Mn2+-PCR, and the amplified DNA was inserted into a plasmid. The plasmid library...
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Published in: | Biological & pharmaceutical bulletin Vol. 30; no. 4; pp. 842 - 844 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Japan
The Pharmaceutical Society of Japan
01-04-2007
Japan Science and Technology Agency |
Subjects: | |
Online Access: | Get full text |
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Summary: | To induce various mutations randomly, PCRs with Mn2+ and with a mutagenic deoxyribonucleotide, 8-hydroxy-dGTP (8-OH-dGTP), were performed. Mutations were induced by deoxyribonucleotide imbalance plus 500 μM Mn2+ in the Mn2+-PCR, and the amplified DNA was inserted into a plasmid. The plasmid library obtained from the transformed bacterial cells was then used as the template in the next PCR, which was done with 50 or 100 μM 8-OH-dGTP. Four kinds of mutations, A:T→G:C and G:C→A:T transitions and A:T→T:A and A:T→C:G transversions, occurred with similar frequencies. These results suggest that this strategy will be useful in random PCR mutagenesis for the in vitro evolution of nucleic acids and proteins, and for analyses of residues in these biomolecules. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0918-6158 1347-5215 |
DOI: | 10.1248/bpb.30.842 |