An analytical method for determining relative specificities for sequential reactions catalyzed by the same enzyme:: Application to the hydrolysis of triacylglycerols by lipases

被引:15
作者
Mitchell, David Alexander [1 ]
Rodriguez, Jorge A. [2 ]
Carriere, Frederic [2 ]
Baratti, Jacques [3 ]
Krieger, Nadia [4 ]
机构
[1] Univ Fed Parana, Dept Bioquim & Biol Mol, Ctr Politecn, BR-81531990 Curitiba, Parana, Brazil
[2] CNRS, Lab Enzymol Interfaciale & Physiol Lipolyse, UPR 9025, Marseille, France
[3] Univ Aix Marseille 2, Grp Biocatalyse & Chimie Fine, Marseille, France
[4] Univ Fed Parana, Dept Quim, Ctr Politecn, BR-81531990 Curitiba, Parana, Brazil
关键词
lipase; mathematical model; specificity constant; triacylglycerol; diacylglycerol; monoacylglycerol; sequential reactions;
D O I
10.1016/j.jbiotec.2007.10.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We propose a model for the sequential hydrolysis of ester bonds of triacylglycerols by lipases and use it as the basis for an analytical method for determining the relative specificity of the lipase for the various substrates with which it can react, when the substrates occur simultaneously in a single reaction system. We then apply the method to our own data and literature data involving the hydrolysis of triacylglycerols by lipases. Our model is able to fit well to most of the reaction profiles, enabling the estimation of relative specificities. We discuss the limitations and potential applications of our method. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:343 / 350
页数:8
相关论文
共 24 条
[1]   Probing the opening of the pancreatic lipase lid using site-directed spin labeling and EPR spectroscopy [J].
Belle, Valerie ;
Fournel, Andre ;
Woudstra, Mireille ;
Ranaldi, Sebastien ;
Prieri, Florence ;
Thome, Virginie ;
Currault, Julie ;
Verger, Robert ;
Guigliarelli, Bruno ;
Carriere, Frederic .
BIOCHEMISTRY, 2007, 46 (08) :2205-2214
[2]   Interfacial enzymology:: The secreted phospholipase A2-paradigm [J].
Berg, OG ;
Gelb, MH ;
Tsai, MD ;
Jain, MK .
CHEMICAL REVIEWS, 2001, 101 (09) :2613-2653
[3]   A MODEL FOR INTERFACIAL ACTIVATION IN LIPASES FROM THE STRUCTURE OF A FUNGAL LIPASE-INHIBITOR COMPLEX [J].
BRZOZOWSKI, AM ;
DEREWENDA, U ;
DEREWENDA, ZS ;
DODSON, GG ;
LAWSON, DM ;
TURKENBURG, JP ;
BJORKLING, F ;
HUGEJENSEN, B ;
PATKAR, SA ;
THIM, L .
NATURE, 1991, 351 (6326) :491-494
[4]   In vivo and in vitro studies on the stereoselective hydrolysis of tri- and diglycerides by gastric and pancreatic lipases [J].
Carriere, F ;
Rogalska, E ;
Cudrey, C ;
Ferrato, F ;
Laugier, R ;
Verger, R .
BIOORGANIC & MEDICINAL CHEMISTRY, 1997, 5 (02) :429-435
[5]   PURIFICATION AND BIOCHEMICAL-CHARACTERIZATION OF DOG GASTRIC LIPASE [J].
CARRIERE, F ;
MOREAU, H ;
RAPHEL, V ;
LAUGIER, R ;
BENICOURT, C ;
JUNIEN, JL ;
VERGER, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 202 (01) :75-83
[6]   Quantitative study of digestive enzyme secretion and gastrointestinal lipolysis in chronic pancreatitis [J].
Carrière, F ;
Grandval, P ;
Renou, C ;
Palomba, A ;
Priéri, F ;
Giallo, J ;
Henniges, F ;
Sander-Struckmeier, S ;
Laugier, R .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2005, 3 (01) :28-38
[7]   How gastric lipase, an interfacial enzyme with a Ser-His-Asp catalytic triad, acts optimally at acidic pH [J].
Chahinian, H ;
Snabe, T ;
Attias, C ;
Fojan, P ;
Petersen, SB ;
Carrière, F .
BIOCHEMISTRY, 2006, 45 (03) :993-1001
[8]  
CHAPUS C, 1981, EUR J BIOCHEM, V115, P99
[9]   QUELQUES REMARQUES COMPLEMENTAIRES SUR LHYDROLYSE DES TRIGLYCERIDES PAR LA LIPASE PANCREATIQUE [J].
CONSTANTIN, MJ ;
PASERO, L ;
DESNUELLE, P .
BIOCHIMICA ET BIOPHYSICA ACTA, 1960, 43 (01) :103-109
[10]   THE 2.46-ANGSTROM RESOLUTION STRUCTURE OF THE PANCREATIC LIPASE-COLIPASE COMPLEX INHIBITED BY A C-11 ALKYL PHOSPHONATE [J].
EGLOFF, MP ;
MARGUET, F ;
BUONO, G ;
VERGER, R ;
CAMBILLAU, C ;
VANTILBEURGH, H .
BIOCHEMISTRY, 1995, 34 (09) :2751-2762