Oligosaccharide hydrolysis by chitosanase enzymes monitored by real-time electrospray ionization-mass spectrometry

被引:28
作者
Dennhart, Nicole [1 ]
Fukamizo, Tamo [2 ]
Brzezinski, Ryszard [3 ]
Lacombe-Harvey, Marie-Eve [3 ]
Letzel, Thomas [1 ]
机构
[1] Tech Univ Munich, Dept Basic Life Sci, Analyt Res Grp, D-85354 Freising Weihenstephan, Germany
[2] Kinki Univ, Dept Adv Biosci, Nara 6318505, Japan
[3] Univ Sherbrooke, Fac Sci, Dept Biol, Ctr Etud & Valorisat Diversite Microbienne, Sherbrooke, PQ J1K 2R1, Canada
基金
日本学术振兴会; 加拿大自然科学与工程研究理事会;
关键词
chitosanase; electrospray ionization; mass spectrometry; enzymatic reaction; oligosaccharide hydrolysis;
D O I
10.1016/j.jbiotec.2008.02.004
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
The chitosanase-catalyzed hydrolysis of chitosan oligosaccharides was investigated for the first time by real-time electrospray ionization-mass spectrometry (ESI-MS). As chitosan oligosaccharides (GlcN, n = 2-6) were hydrolyzed by exochitosanase (exo-beta-glucosaminidase) from Amycolatopsis orientalis, the reaction time-courses of substrate, intermediate and products could be monitored simultaneously by direct infusion of the reaction solvent into the mass spectrometer. Consequently, the analytical approach of real-time MS is an enormous time-saving method. Furthermore, the high sensitivity of the mass spectrometric detection allows the determination of the reaction time-courses with very low quantities of substrate and therefore also a low amount of applied enzyme. Real-time mass spectrometric detection was also applicable in investigating the reaction behaviour of Streptomyces sp. N174 endochitosanase wild type and of two of its mutants. This technique establishes the fast and efficient determination of in vitro enzymatic activities of various enzyme systems. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:253 / 260
页数:8
相关论文
共 24 条
[11]   Chitinolytic Enzymes: Catalysis, Substrate Binding, and their Application [J].
Fukamizo, Tamo .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2000, 1 (01) :105-124
[12]   Kinetic measurements of phosphoglucose isomerase and phosphomannose isomerase by direct analysis of phosphorylated aldose-ketose isomers using tandem mass spectrometry [J].
Gao, H ;
Chen, Y ;
Leary, JA .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2005, 240 (03) :291-299
[13]   Chitosanase-catalyzed hydrolysis of 4-methylumbelliferyl β-chitotrioside [J].
Honda, Y ;
Kirihata, M ;
Fukamizo, T ;
Kaneko, S ;
Tokuyasu, K ;
Brzezinski, R .
JOURNAL OF BIOCHEMISTRY, 1999, 126 (03) :470-474
[14]   Role of acidic amino acid residues in chitooligosaccharide-binding to Streptomyces sp N174 chitosanase [J].
Katsumi, T ;
Lacombe-Harvey, ME ;
Tremblay, H ;
Brzezinski, R ;
Fukamizo, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 338 (04) :1839-1844
[15]   STRUCTURE-BASED DESIGN OF A LYSOZYME WITH ALTERED CATALYTIC ACTIVITY [J].
KUROKI, R ;
WEAVER, LH ;
MATTHEWS, BW .
NATURE STRUCTURAL BIOLOGY, 1995, 2 (11) :1007-1011
[16]   REAL-TIME REACTION MONITORING BY CONTINUOUS-INTRODUCTION ION-SPRAY TANDEM MASS-SPECTROMETRY [J].
LEE, ED ;
MUCK, W ;
HENION, JD ;
COVEY, TR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (13) :4600-4604
[17]   SOME EFFECTS OF CHITOSAN ON LIVER-FUNCTION IN THE RAT [J].
LEHOUX, JG ;
GRONDIN, F .
ENDOCRINOLOGY, 1993, 132 (03) :1078-1084
[18]   Monitoring enzymatic conversions by mass spectrometry: a critical review [J].
Liesener, A ;
Karst, U .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2005, 382 (07) :1451-1464
[19]   X-ray structure of an anti-fungal chitosanase from Streptomyces N174 [J].
Marcotte, EM ;
Monzingo, AF ;
Ernst, SR ;
Brzezinski, R ;
Robertus, JD .
NATURE STRUCTURAL BIOLOGY, 1996, 3 (02) :155-162
[20]   HOW TO MEASURE AND PREDICT THE MOLAR ABSORPTION-COEFFICIENT OF A PROTEIN [J].
PACE, CN ;
VAJDOS, F ;
FEE, L ;
GRIMSLEY, G ;
GRAY, T .
PROTEIN SCIENCE, 1995, 4 (11) :2411-2423