ON THE IMPORTANCE OF THE SUPPORT MATERIAL FOR ENZYMATIC-SYNTHESIS IN ORGANIC MEDIA - SUPPORT EFFECTS AT CONTROLLED WATER ACTIVITY

被引:143
作者
ADLERCREUTZ, P
机构
[1] Department of Biotechnology, Chemical Center, University of Lund
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1991年 / 199卷 / 03期
关键词
D O I
10.1111/j.1432-1033.1991.tb16161.x
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
Enzymes were deposited on different porous support materials and these preparations were used to catalyze reactions in organic media. Reactions were carried out at specific water activities, achieved by equilibrating both the enzyme preparation and the substrate solution at the desired water activity before mixing them and thereby starting the reactions. The reaction rates obtained at the same water activity with different supports differed greatly, indicating a direct influence of the support on the enzyme. For horse liver alcohol dehydrogenase, Celite was the best support, and the reaction rate increased with increasing water activity. In the alpha-chymotrypsin-catalyzed alcoholysis of N-acetyl-L-phenylalanine ethyl ester with 1-butanol, high rates were again obtained with Celite, but with this support only about one third of the ethyl ester was converted to butyl ester, the rest was hydrolyzed. With the polyamide support, Accurel PA6, alcoholysis was the dominating reaction, and by using a low water activity (0.33), hydrolysis was completely suppressed while still maintaining a high alcoholysis activity. Controlled pore glass (CPG), derivatized with either hexyl or glucosyl groups, had quite different properties as enzyme supports. For horse liver alcohol dehydrogenase, glucose-CPG was a much better support than hexyl-CPG, and in the alpha-chymotrypsin-catalyzed reactions, glucose-CPG favored hydrolysis, and hexyl-CPG alcoholysis, at water activities exceeding 0.8. The results are discussed considering the absorption of water on the enzymes, on the supports and the solubility of water in the reaction media; all these parameters were measured separately.
引用
收藏
页码:609 / 614
页数:6
相关论文
共 16 条
[1]   ENZYMATIC OXIDATION OF ETHANOL IN THE GASEOUS-PHASE [J].
BARZANA, E ;
KAREL, M ;
KLIBANOV, AM .
BIOTECHNOLOGY AND BIOENGINEERING, 1989, 34 (09) :1178-1185
[2]   ENZYMATIC CATALYSIS IN MONOPHASIC ORGANIC-SOLVENTS [J].
DORDICK, JS .
ENZYME AND MICROBIAL TECHNOLOGY, 1989, 11 (04) :194-211
[3]  
Drapron R., 1985, PROPERTIES WATER FOO, P171, DOI DOI 10.1007/978-94-009-5103-7_11
[4]   LIPASE-CATALYZED ESTER EXCHANGE-REACTIONS IN ORGANIC MEDIA WITH CONTROLLED HUMIDITY [J].
GODERIS, HL ;
AMPE, G ;
FEYTEN, MP ;
FOUWE, BL ;
GUFFENS, WM ;
VANCAUWENBERGH, SM ;
TOBBACK, PP .
BIOTECHNOLOGY AND BIOENGINEERING, 1987, 30 (02) :258-266
[5]   THE CONTROL OF LIPASE-CATALYZED TRANSESTERIFICATION AND ESTERIFICATION REACTION-RATES - EFFECTS OF SUBSTRATE POLARITY, WATER ACTIVITY AND WATER-MOLECULES ON ENZYME-ACTIVITY [J].
GOLDBERG, M ;
THOMAS, D ;
LEGOY, MD .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 190 (03) :603-609
[6]   HUMIDITY FIXED-POINTS OF BINARY SATURATED AQUEOUS-SOLUTIONS [J].
GREENSPAN, L .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS SECTION A-PHYSICS AND CHEMISTRY, 1977, 81 (01) :89-96
[7]   HIGH-AFFINITY BINDING OF WATER BY PROTEINS IS SIMILAR IN AIR AND IN ORGANIC-SOLVENTS [J].
HALLING, PJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1040 (02) :225-228
[8]   APPLICATION OF POLYETHYLENE GLYCOL-MODIFIED ENZYMES IN BIOTECHNOLOGICAL PROCESSES - ORGANIC SOLVENT-SOLUBLE ENZYMES [J].
INADA, Y ;
TAKAHASHI, K ;
YOSHIMOTO, T ;
AJIMA, A ;
MATSUSHIMA, A ;
SAITO, Y .
TRENDS IN BIOTECHNOLOGY, 1986, 4 (07) :190-194
[9]  
LAANE C, 1987, BIOCATALYSIS ORGANIC
[10]   THERMODYNAMIC FUNCTIONS OF BIO-POLYMER HYDRATION .1. THEIR DETERMINATION BY VAPOR-PRESSURE STUDIES, DISCUSSED IN AN ANALYSIS OF THE PRIMARY HYDRATION PROCESS [J].
LUSCHERMATTLI, M ;
RUEGG, M .
BIOPOLYMERS, 1982, 21 (02) :403-418