L-Valine is a branched-chain amino acid that is synthesized through a metabolic pathway utilizing 2-ketoisovalerate (KIV) as a direct intermediate [94]. The biosynthesis of this amino acid involves enzymes such as acetohydroxy acid synthase (AHAS) and acetolactate synthase (AlsS), which are responsible for early steps in the branched-chain amino acid pathway [94].
The L-valine biosynthetic pathway serves as a foundational platform for the microbial production of biofuels and commodity chemicals [94]. A key engineering approach involves diverting the pathway intermediate 2-ketoisovalerate to produce isobutanol through the heterologous expression of 2-ketoacid decarboxylase (Kdc) and alcohol dehydrogenase (Adh) [94, 98]. Strategies to optimize L-valine production include systems metabolic engineering, which integrates transcriptome profiling and in silico genome-scale metabolic network simulations to identify genetic targets for modification [200, 363]. Additionally, guided evolution and adaptive laboratory evolution are utilized as strategies to develop high-performing microbial cell factories by optimizing metabolic flux and host fitness [363].
L-valine
Description
Chemical Formula:
C5H11NO2
Molecular Weight:
117.147 Daltons
Monoisotopic Mass:
118.0868036346 Daltons
SMILES:
CC(C)C([N+])C([O-])=O
InChI:
1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/t4-/m0/s1
InChIKey:
Synonyms
- V
- valine
- L-val
- 2-Amino-3-methylbutyric acid
Databases
MetaCyc:
VAL
RefMet:
Valine
BiGG:
val__L
MetaboLights:
MTBLC57762
HMDB:
HMDB00883
KEGG:
C00183
CAS:
72-18-4
MediaDB:
compounds/14807/
compounds/179/
MetaNetX:
MNXM199
PupChem (SID):
3483
CHEMBL:
CHEMBL43068
KNApSAcK:
C00001398
PDB-CCD:
VAL
3DMET:
B00054
NIKKAJI:
J9.179K