Influence of pH on the Formation of Glucan by Lactobacillus reuteri TMW 1.106 Exerting a Protective Function Against Extreme pH Values

被引:21
作者
Kaditzky, Susanne B. [1 ]
Behr, Jurgen [1 ]
Stocker, Andreas [2 ]
Kaden, Peter [3 ]
Gaenzle, Michael G. [4 ]
Vogel, Rudi F. [1 ]
机构
[1] Tech Univ Munich, D-85350 Freising Weihenstephan, Germany
[2] GSF Natl Res Ctr Environm & Hlth, Inst Ecol Chem, Neuherberg, Germany
[3] Tech Univ Munich, Dept Chem Organ Chem & Biochem 2, D-8046 Garching, Germany
[4] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB, Canada
关键词
Lactobacillus reuteri; pH value; exopolysaccharides; dextran; protective function;
D O I
10.1080/08905430802470235
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 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Lactobacillus reuteri TMW 1.106, a dominant type II sourdough bacterium, produces glucan from sucrose in vitro and in situ. Exopolysaccharides positively affect the texture and mouth feel of foods and their in situ production in fermented foods could be an alternative to the addition of hydrocolloids from plants or non-GRAS microorganisms. The aim of this study was to elucidate a probable function of the EPS for the bacterium. Lb. reuteri TMW 1.106 harbors two glucosyltransferases, Gtf106A and Gtf106B and produces a dextran. Gtf106B exhibited hydrolysis but no transferase activity. Enzymatic production of dextran with the heterologously expressed, N-terminally truncated N Gtf106A was highest at a pH of 4.0, whereas dextran formation in pH static fermentations was optimal between pH 4.7 and 5.4. The dextran synthesised at these pH values had the highest molecular mass (1.2 107) and 15% -(1-4) linkages. A protective effect of this EPS on Lb. reuteri TMW 1.106 against low pH, explaining the low pH-production maximum, could be demonstrated through the delay of cell death.
引用
收藏
页码:398 / 418
页数:21
相关论文
共 44 条
[1]
PEPTIDE SEQUENCES FOR SUCROSE SPLITTING AND GLUCAN BINDING WITHIN STREPTOCOCCUS-SOBRINUS GLUCOSYLTRANSFERASE (WATER-INSOLUBLE GLUCAN SYNTHETASE) [J].
ABO, H ;
MATSUMURA, T ;
KODAMA, T ;
OHTA, H ;
FUKUI, K ;
KATO, K ;
KAGAWA, H .
JOURNAL OF BACTERIOLOGY, 1991, 173 (03) :989-996
[2]
Size and structure characterization of ethylhydroxyethyl cellulose by the combination of field-flow fractionation with other techniques.: Investigation of ultralarge components [J].
Andersson, M ;
Wittgren, B ;
Schagerlöf, H ;
Momcilovic, D ;
Wahlund, KG .
BIOMACROMOLECULES, 2004, 5 (01) :97-105
[3]
[Anonymous], 1989, Molecular Cloning
[4]
Environmental influences on exopolysaccharide formation in Lactobacillus reuteri ATCC 55730 [J].
Arskold, Emma ;
Svensson, Malin ;
Grage, Halfdan ;
Roos, Stefan ;
Radstrom, Peter ;
van Niel, Ed W. J. .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2007, 116 (01) :159-167
[5]
Techniques for studying protein heterogeneity and post-translational modifications [J].
Baumann, M ;
Meri, S .
EXPERT REVIEW OF PROTEOMICS, 2004, 1 (02) :207-217
[6]
BEHR J, 2007, APPL ENV MI IN PRESS
[7]
Bread technology and sourdough technology [J].
Decock, P ;
Cappelle, S .
TRENDS IN FOOD SCIENCE & TECHNOLOGY, 2005, 16 (1-3) :113-120
[8]
Devulpalle KS, 1997, PROTEIN SCI, V6, P2489
[9]
GIDLEY MJ, 1985, CARBOHYD RES, V139, P85
[10]
Karlson P, 1994, Kurzes lehrbuch der biochemie fur mediziner und naturwissenschaftler, V14th