Biotechnological applications of Candida antarctica lipase A:: State-of-the-art

被引:169
作者
de María, PD [1 ]
Carboni-Oerlemans, C [1 ]
Tuin, B [1 ]
Bargeman, G [1 ]
van der Meer, A [1 ]
van Gemert, R [1 ]
机构
[1] Akzo Nobel Chem BV, Chem & Proc Technol Dept, NL-6800 SB Arnhem, Netherlands
关键词
Candida antarctica lipase A; thermostability; trans-fatty acids selectivity; chemoselective N-acylation; amino acids; tertiary alcohols;
D O I
10.1016/j.molcatb.2005.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The yeast Candida antarctica produces two different lipases, lipases A band B. While lipase B (CAL-B) is probably the mostly employed hydrolase in the biocatalysis field, the use of the lipase A (CAL-A) has been rather scarce and consequently its tridimensional structure has not been elucidated yet. However, CAL-A is a useful biocatalyst with many different applications that have been described especially in the last few years. Its attractiveness results from its unique features among hydrolases: the high thermostability, allowing operation at T > 90 degrees C; the ability to accept tertiary and sterically hindered alcohols, which has recently been attributed to the existence of a specific aminoacidic sequence in the active site; the sn-2 recognition in hydrolysis of triglycerides; the selectivity towards trans-fatty acids; the stability in the acidic pH range. Furthermore, it is considered to be an excellent biocatalyst for the asymmetric synthesis of amino acids/amino esters, due to its chemoselectivity towards amine groups. Considering all these aspects, in the present review, the origin, the properties and the applications of the CAL-A are briefly described and discussed, pointing out the unique characteristics of this biocatalyst. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:36 / 46
页数:11
相关论文
共 78 条
[1]   One biocatalyst - Many applications: The use of Candida antarctica B-lipase in organic synthesis [J].
Anderson, EM ;
Karin, M ;
Kirk, O .
BIOCATALYSIS AND BIOTRANSFORMATION, 1998, 16 (03) :181-204
[2]   Regioselective enzymatic acylation of methyl shikimate.: Influence of acyl chain length and solvent polarity on enzyme specificity [J].
Armesto, N ;
Ferrero, M ;
Fernández, S ;
Gotor, V .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (14) :4978-4981
[3]   Novel enzymatic synthesis of 4-O-cinnamoyl quinic and shikimic acid derivatives [J].
Armesto, N ;
Ferrero, M ;
Fernández, S ;
Gotor, V .
JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (14) :5784-5787
[4]   Enzymatic removal of carboxyl protecting groups. 2. Cleavage of the benzyl and methyl moieties [J].
Barbayianni, E ;
Fotakopoulou, I ;
Schmidt, M ;
Constantinou-Kokotou, V ;
Bornscheuer, UT ;
Kokotos, G .
JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (22) :8730-8733
[5]  
BORCH K, 2001, Patent No. 0153511A1
[6]   Substrate selectivity of various lipases in the esterification of cis- and trans-9-octadecenoic acid [J].
Borgdorf, R ;
Warwel, S .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1999, 51 (04) :480-485
[7]  
BORNSCHEUER UT, 1999, HYDROLASES ORG CHEM
[8]  
Bosley J. A., 1997, US Patent, Patent No. [5,658,769, 5658769]
[9]  
BOSLEY JA, 1995, Patent No. 9501450
[10]   Alcoholysis of waste fats with 2-ethyl-1-hexanol using Candida antarctica lipase A in large-scale tests [J].
Brenneis, R ;
Baeck, B ;
Kley, G .
EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, 2004, 106 (12) :809-814