Literature DB >> 24458258

[Sucrose metabolizing enzymes in roots].

G H Vieweg1.   

Abstract

In tomato, pea, and maize roots, the presence of sucrose synthetase (E.C. 2.4.1.13), sucrose phosphate synthetase (E.C. 2.4.1.14), and both the alkaline and acid sucrases (E.C. 3.2.1.? and E.C. 3.2.1.26) could be demonstrated. The activity of these enzymes was measured directly on root slices suspended in the incubation mixture, which also contained 10% dimethyl sulfoxide or 5% ethyl acetate. These two additives increase the permeability of the membranes, thus allowing the entry of substrates to the site where the enzymes are located and favouring the release of products into the medium. The values found by measuring the activities of sucrose synthetase and the alkaline sucrase on tomato root were quite comparable to those obtained using enzymic preparations of the same tissue. In the case of the weakly active sucrose phosphate synthetase and the very active acid sucrase, the comparison of the two methods showed that losses of activity occurred during the preparation of the enzymes. By separating stele from cortex in tomato and maize roots, it could be shown that sucrose phosphate synthetase is located only in the stele, while the other enzymes are unevenly distributed between the two tissues, the sucrases predominating in the cortex. Sucrose phosphate synthetase and sucrose synthetase are most active in the region with root hairs of maize roots, while the activity of both sucrases is higher in the region near the apex. The highest invertase activity was measured in the apex of stem-borne adventitious roots that had not yet penetrated the soil. In older roots, sucrose phosphate synthetase disappears and the activity of all the other enzymes diminishes. It is suggested that the high activity of sucrose synthetase is present in the regions where an active synthesis of cell wall substances from glycosyl nucleotides is taking place, while the sucrases provide the initial substrates for most of the other pathways.

Entities:  

Year:  1974        PMID: 24458258     DOI: 10.1007/BF00390858

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.116


  11 in total

1.  The synthesis of sucrose by extracts of the root of the sugar beet.

Authors:  J V DUTTON; A CARRUTHERS
Journal:  Biochem J       Date:  1961-11       Impact factor: 3.857

2.  Sucrose phosphate synthesis in wheat germ and green leaves.

Authors:  J MENDICINO
Journal:  J Biol Chem       Date:  1960-12       Impact factor: 5.157

3.  Synthesis of a beta-1, 3-linked glucan by extracts of Phaseolus aureus seedlings.

Authors:  D S FEINGOLD; E F NEUFELD; W Z HASSID
Journal:  J Biol Chem       Date:  1958-10       Impact factor: 5.157

4.  A technique for the assay of enzymes in intact plant cells in the presence of dimethylsulfoxide.

Authors:  D P Delmer; S E Mills
Journal:  Plant Physiol       Date:  1969-01       Impact factor: 8.340

5.  [Enzymes of starch metabolism in root cap cells of Zea mays L].

Authors:  W Huber; M A de Fekete; H Ziegler
Journal:  Planta       Date:  1973-12       Impact factor: 4.116

6.  [Exchange mechanism of ion transport in corn roots].

Authors:  J Weigl
Journal:  Planta       Date:  1968-09       Impact factor: 4.116

7.  [G-1-P as precursor for starch synthesis in bundle sheath cells of Zea mays].

Authors:  G H Vieweg; M A de Fekete
Journal:  Planta       Date:  1972-09       Impact factor: 4.116

Review 8.  Biosynthesis of oligosaccharides and polysaccharides in plants.

Authors:  W Z Hassid
Journal:  Science       Date:  1969-07-11       Impact factor: 47.728

9.  The regulative properties of UDPglucose: D-fructose-6-phosphate 2-glucosyltransferase (sucrose phosphate synthetase) from Vicia faba cotyledons.

Authors:  M A de Fekete
Journal:  Eur J Biochem       Date:  1971-03-01

10.  The Biosynthesis of Sucrose and Nucleoside Diphosphate Glucoses in Phaseolus aureus.

Authors:  D P Delmer; P Albersheim
Journal:  Plant Physiol       Date:  1970-06       Impact factor: 8.340

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.