Adenine → L-Lysine
Reaction equation
[NH2:1][C@H:2]([C:9]([OH:11])=[O:10])[CH2:3][C:4]1N=CN[CH:5]=1.[N:12]1C(N)=C2C(N=CN2)=N[CH:13]=1>>[NH2:1][C@H:2]([C:9]([OH:11])=[O:10])[CH2:3][CH2:4][CH2:5][CH2:13][NH2:12]Participants
Reactant 2
Product 1
Procedure
An ADE2 fragment and a LYS2 fragment were also prepared under similar reaction conditions using A451 genomic DNA as a template and ADE-1 (5′ ATG GAT TCT AGA ACA GTT GGT 3′ (SEQ ID NO: 127)) and ADE-2 (5′ TTA CTT GTT TTC TAG ATA AGC 3′ (SEQ ID NO: 128)) or LYS-1 (5′ ATG ACT AAC GAA AAG GTC TGG 3′ (SEQ ID NO: 129)) and LYS-2 (5′ TTA AGC TGC TGC GGA GCT TCC 3′ (SEQ ID NO: 130)) as primer DNAs. The resultant HIS3 fragment and ADE2 fragment were introduced into pRS435GGF/YH1 successively to thereby obtain pRS435GGF/YH1-AH that exhibited non-histidine requirement and non-adenine requirement as phenotypes. On the other hand, the LYS2 fragment and URA3 fragment were introduced into YPH500 successively to thereby obtain YPH500-KU that exhibited non-lysine requirement and non-uracil requirement as phenotypes.
Workup
- customAn ADE2 fragment and a LYS2 fragment were also prepared under similar reaction conditions
- additionThe resultant HIS3 fragment and ADE2 fragment were introduced into pRS435GGF/YH1 successively to thereby obtain pRS435GGF/
- additionOn the other hand, the LYS2 fragment and URA3 fragment were introduced into YPH500 successively
Sources & evidence
- ORD record
- ord-4bbbb27521d247fb9f8aa4127e917a6f
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07501268B2
Reaction notes
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