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Reaction conditions for the resolution of 2-methylalkanoic acids in esterification and hydrolysis with lipase from Candida cylindracea

Holmberg, Erland (author)
KTH,Biokemi och biokemisk teknologi
Holmquist, Mats Torsten (author)
KTH,Biokemi och biokemisk teknologi
Hedenström, Erik (author)
Mittuniversitetet,Institutionen för naturvetenskap (-2008),University College of Sundsvall/Härnösand, Box 860, S-851 24, Sundsvall, Sweden
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Berglund, P. (author)
Mittuniversitetet,Institutionen för naturvetenskap (-2008),University College of Sundsvall/Härnösand, Box 860, S-851 24, Sundsvall, Sweden
Norin, Torbjörn (author)
KTH,Organisk kemi
Högberg, Hans-Erik (author)
Mittuniversitetet,Institutionen för naturvetenskap (-2008),University College of Sundsvall/Härnösand, Box 860, S-851 24, Sundsvall, Sweden
Hult, Karl (author)
KTH,Biokemi och biokemisk teknologi
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 (creator_code:org_t)
1991
1991
English.
In: Applied Microbiology and Biotechnology. - 0175-7598. ; 35:5, s. 572-578
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We have demonstrated resolution of 2-methylalkanoic acids using lipase from Candida cylindracea as a catalyst. The resolution of 2-methyldecanoic acid was more successful than that of 2-methylbutyric acid both by esterification and hydrolysis. This indicates that the resolution of the acid is dependent on the chain length of the acid moiety. The chain length of the alcohol moiety of the ester affected the resolution of the long-chain acid only. Using esterification, (R)-2-methyldecanoic acid was produced in an enantiomeric excess (e.e.) of 95% (E = 40). If the enantiomeric ratio is low (E = 3.6), as in the resolution of 2-methylbutyric acid, esterification combined with a high equilibrium conversion could be used to yield the remaining acid in a high e.e. In the hydrolytic reactions, the e.e. and the equilibrium conversion were dependent on the pH and the presence of CaCl2. When octyl 2-methyldecanoate was hydrolysed at pH 8.0 in the presence of CaCl2, the (S)-acid was formed with an e.e. of 80% (E = 9), but when the hydrolysis was carried out at pH 7.5 without CaCl2, a very low e.e. and a low equilibrium conversion were observed. The latter conditions allowed the esterification of 2-methyldecanoic acid with 1-octanol even in aqueous medium.

Subject headings

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology (hsv//eng)

Keyword

2 methylalkanoic acid
triacylglycerol lipase
unclassified drug
article
biotechnology
candida
esterification
hydrolysis
nonhuman
Candida cylindracea
Chemistry
Bioengineering

Publication and Content Type

ref (subject category)
art (subject category)

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