Literature DB >> 5122

A quantitation of the factors which affect the hydrolase and transgalactosylase activities of beta-galactosidase (E. coli) on lactose.

R E Huber, G Kurz, K Wallenfels.   

Abstract

A study was implemented to quantitate the hydrolase and transgalactosylase activities of beta-galactosidase (E. coli) with lactose as the substrate and to investigate various factors which affect these activities. At low lactose concentrations the rate of galactose production was equal to the rate of glucose production. The rate of galactose production relative to glucose, however, dropped dramatically at lactose concentrations higher than 0.05 M and production of trisaccharides and tetrasaccharides began (galactose/glucose ratios of about 2:1 and 3:1, respectively, were found for these two types of oligosaccharides). At least five different trissacharides were formed and their patterns of formation showed that they probably utilized both lactose and allolactose as galactosyl acceptors. Allolactose was produced in amounts proportional to glucose at all lactose concentrations (ratios of allolactose/glucose were about 0.88). Analyses of various data, including a reaction analyzed at very early times, showed that the major means of production of allolactose (and the only means initially) was the direct enzymatic transfer of galactose from the 4 position to the 6 position of the glucose moiety of lactose without prior release of glucose from the enzyme. It was shown, however, that allolactose could also be formed in significant quantities by the transfer of galactose to the 6 position of free glucose, and also by hydrolysis of preformed trisaccharide. A mechanism which fits the initial velocity data was proposed in which the steps involving the formation of an enzyme-gallactose-glucose complex, the formation and breakage of allolactose on the enzyme, and the release of glucose all seem to be of roughly equal magnitude and rate determining. Various factors affected the amounts of transgalactosylase and hydrolase activities occurring. At high pH values (greater than 7.8) the transgalactosylase/hydrolyase activity ratio increased dramatically while it decreased at low pH values (less than 6.0). At mid pH values the ratio was essentially constant. The absence of Mg2+ caused a large decrease in the transgalactosylase/hydrolase activity ratio while the absence of all but traces of Na+ or K+ had no effect. The anomeric configuration of lactose altered the transgalactosylase/hydrolase activity ratios, alpha-Lactose resulted in a decrease of allolactose production (transgalactosylase activity) relative to hydrolase activities (glucose production) while beta-lactose had the opposite effect.

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Year:  1976        PMID: 5122     DOI: 10.1021/bi00654a029

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  35 in total

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Authors:  Necmettin Yildirim; Michael C Mackey
Journal:  Biophys J       Date:  2003-05       Impact factor: 4.033

3.  Studying enzymatic bioreactions in a millisecond microfluidic flow mixer.

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4.  Direct and indirect roles of His-418 in metal binding and in the activity of beta-galactosidase (E. coli).

Authors:  Douglas H Juers; Beatrice Rob; Megan L Dugdale; Nastaron Rahimzadeh; Clarence Giang; Michelle Lee; Brian W Matthews; Reuben E Huber
Journal:  Protein Sci       Date:  2009-06       Impact factor: 6.725

5.  Selection and neutrality in lactose operons of Escherichia coli.

Authors:  A M Dean
Journal:  Genetics       Date:  1989-11       Impact factor: 4.562

6.  PDZ affinity chromatography: a general method for affinity purification of proteins based on PDZ domains and their ligands.

Authors:  Ward G Walkup; Mary B Kennedy
Journal:  Protein Expr Purif       Date:  2014-03-06       Impact factor: 1.650

7.  Novel inducers of the xylan-degrading enzyme system of Cryptococcus albidus.

Authors:  P Biely; E Petráková
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

8.  Structural explanation for allolactose (lac operon inducer) synthesis by lacZ β-galactosidase and the evolutionary relationship between allolactose synthesis and the lac repressor.

Authors:  Robert W Wheatley; Summie Lo; Larisa J Jancewicz; Megan L Dugdale; Reuben E Huber
Journal:  J Biol Chem       Date:  2013-03-13       Impact factor: 5.157

9.  Studies of Glu-416 variants of beta-galactosidase (E. coli) show that the active site Mg(2+) is not important for structure and indicate that the main role of Mg (2+) is to mediate optimization of active site chemistry.

Authors:  Summie Lo; Megan L Dugdale; Nisha Jeerh; Tabitha Ku; Nathan J Roth; Reuben E Huber
Journal:  Protein J       Date:  2010-01       Impact factor: 2.371

10.  Studies on the utilization of lactose by Corynebacterium glutamicum, bearing the lactose operon of Escherichia coli.

Authors:  W Brabetz; W Liebl; K H Schleifer
Journal:  Arch Microbiol       Date:  1991       Impact factor: 2.552

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