2-acetolactate

2-acetolactate is a lipid of Fatty Acyls (FA) class.

Cross Reference

There are no associated biomedical information in the current reference collection.

Current reference collection contains 253 references associated with 2-acetolactate in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.


Here are additional resources we collected from PubChem and MeSH for 2-acetolactate

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with 2-acetolactate

MeSH term MeSH ID Detail
Lung Neoplasms D008175 171 associated lipids
Total 1

PubChem Biomolecular Interactions and Pathways

NCBI Entrez Crosslinks

All references with 2-acetolactate

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Authors Title Published Journal PubMed Link
Duong CT et al. Identification of Sc-type ILV6 as a target to reduce diacetyl formation in lager brewers' yeast. 2011 Metab. Eng. pmid:21824525
Monnet C et al. Regulation of branched-chain amino acid biosynthesis by alpha-acetolactate decarboxylase in Streptococcus thermophilus. 2003 Lett. Appl. Microbiol. pmid:12753249
Yu Q et al. AHAS herbicide resistance endowing mutations: effect on AHAS functionality and plant growth. 2010 J. Exp. Bot. pmid:20627897
Kobayashi K et al. Method for the simultaneous assay of diacetyl and acetoin in the presence of alpha-acetolactate: application in determining the kinetic parameters for the decomposition of alpha-acetolactate. 2005 J. Biosci. Bioeng. pmid:16233823
Hu W et al. Selective editing of Val and Leu methyl groups in high molecular weight protein NMR. 2012 J. Biomol. NMR pmid:22532128
Moreno-Sánchez R et al. Metabolic control analysis: a tool for designing strategies to manipulate metabolic pathways. 2008 J. Biomed. Biotechnol. pmid:18629230
Nemeria N et al. Glutamate 636 of the Escherichia coli pyruvate dehydrogenase-E1 participates in active center communication and behaves as an engineered acetolactate synthase with unusual stereoselectivity. 2005 J. Biol. Chem. pmid:15802265
Pang SS et al. The crystal structures of Klebsiella pneumoniae acetolactate synthase with enzyme-bound cofactor and with an unusual intermediate. 2004 J. Biol. Chem. pmid:14557277
Engel S et al. Role of a conserved arginine in the mechanism of acetohydroxyacid synthase: catalysis of condensation with a specific ketoacid substrate. 2004 J. Biol. Chem. pmid:15044456
Le Bars D and Yvon M Formation of diacetyl and acetoin by Lactococcus lactis via aspartate catabolism. 2008 J. Appl. Microbiol. pmid:17850313