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1.
J Org Chem ; 72(3): 782-6, 2007 Feb 02.
Article in English | MEDLINE | ID: mdl-17253795

ABSTRACT

An esterase from Bacillus subtilis (BS2) allows the fast and selective removal of allyl, 2-chloroethyl, and 2,2,2-chloroethyl esters under mild conditions in high yields. In addition, BS2 easily hydrolyzes phenacyl esters, while the hydrolysis of sterically hindered diphenylmethyl esters is slow, requiring longer reaction time and higher enzyme/substrate ratio.


Subject(s)
Allyl Compounds/metabolism , Bacillus subtilis/enzymology , Carboxylic Acids/metabolism , Esterases/metabolism , Esters/metabolism , Ethyl Chloride/metabolism , Allyl Compounds/chemistry , Carboxylic Acids/chemistry , Esterases/chemistry , Esters/chemistry , Ethyl Chloride/analogs & derivatives , Hydrolysis , Models, Chemical , Time Factors
2.
J Org Chem ; 70(22): 8730-3, 2005 Oct 28.
Article in English | MEDLINE | ID: mdl-16238302

ABSTRACT

[reaction: see text] Enzymes are versatile reagents for the efficient removal of methyl and benzyl protecting groups. An esterase from Bacillus subtilis (BS2) and a lipase from Candida antarctica (CAL-A) allow a mild and selective removal of these moieties in high yields without affecting other functional groups.


Subject(s)
Benzene/chemistry , Lipase/metabolism , Pancreatic Elastase/metabolism , Bacillus subtilis/enzymology , Candida/enzymology , Esters/chemistry , Hydrolysis , Lipase/chemistry , Methylation , Molecular Structure , Pancreatic Elastase/chemistry , Peptides/chemistry , Peptides/metabolism , Phospholipases A/antagonists & inhibitors
3.
J Org Chem ; 70(9): 3737-40, 2005 Apr 29.
Article in English | MEDLINE | ID: mdl-15845019

ABSTRACT

[reaction: see text] A recent discovery that a certain amino acid motif (GGG(A)X-motif) in lipases and esterases determines their activity toward tertiary alcohols prompted us to investigate the use of these biocatalysts in the mild and selective removal of tert-butyl protecting groups in amino acid derivatives and related compounds. An esterase from Bacillus subtilis (BsubpNBE) and lipase A from Candida antarctica (CAL-A) were identified as the most active enzymes, which hydrolyzed a range of tert-butyl esters of protected amino acids (e.g., Boc-Tyr-O(t)Bu, Z-GABA-O(t)Bu, Fmoc-GABA-O(t)Bu) in good to high yields and left Boc, Z, and Fmoc-protecting groups intact.


Subject(s)
Bacillus subtilis/enzymology , Benzene Derivatives/metabolism , Candida albicans/enzymology , Esterases/metabolism , Hydrocarbons, Halogenated/metabolism , Lipase/metabolism , Amino Acid Sequence , Amino Acids , Butanes/chemical synthesis , Butanes/metabolism , Carboxylic Acids/metabolism , Catalysis , Indicators and Reagents
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