Literature DB >> 16664772

Quantitative Measurements of Hexokinase Activity in the Shoot Apical Meristem, Leaf Primordia, and Leaf Tissues of Dianthus chinensis L.

J G Croxdale1, P J Vanderveer.   

Abstract

Hexokinase was measured by quantitative histochemical techniques in the apical meristem, primordia, and leaves of Dianthus chinensis L. The structural stages of development in the leaves sampled were determined by light and scanning electron microscopy. The results showed that activity decreased from the youngest primordia (1500 millimoles per kilogram dry weight per hour) to the mature leaves (200 millimoles per kilogram dry weight per hour) and that an intermediate leaf, the fourth youngest, showed the same declining pattern from its base to its tip. Surface views and measurements of these leaves revealed their basipetal maturation as seen by cell size, stomatal development, trichome differentiation, cuticular appearance, and leaf thickness. The intermediate leaf showed features representative of several stages in structural differentiation. It was concluded that the changes in hexokinase activity among the leaves of a shoot and within an individual leaf are similar and correlate with the degree of structural differentiation of the leaves.

Entities:  

Year:  1986        PMID: 16664772      PMCID: PMC1075304          DOI: 10.1104/pp.81.1.186

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  10 in total

1.  Chlorophyll, Ribulose-1,5-diphosphate Carboxylase, and Hill Reaction Activity in Developing Leaves of Populus deltoides.

Authors:  D I Dickmann
Journal:  Plant Physiol       Date:  1971-08       Impact factor: 8.340

2.  Enzymic and substrate basis for the anaplerotic step in guard cells.

Authors:  W H Outlaw; J Kennedy
Journal:  Plant Physiol       Date:  1978-10       Impact factor: 8.340

3.  Quantitative Measurements of Phosphofructokinase in the Shoot Apical Meristem, Leaf Primordia, and Leaf Tissues of Dianthus chinensis L.

Authors:  J G Croxdale
Journal:  Plant Physiol       Date:  1983-09       Impact factor: 8.340

4.  The stability of pyridine nucleotides.

Authors:  O H LOWRY; J V PASSONNEAU; M K ROCK
Journal:  J Biol Chem       Date:  1961-10       Impact factor: 5.157

5.  Quantitative histochemical analysis of glycolytic intermediates and cofactors with an oil well technique.

Authors:  F M Matschinsky; J V Passonneau; O H Lowry
Journal:  J Histochem Cytochem       Date:  1968-01       Impact factor: 2.479

6.  Influence of Cell Age on Chlorophyll Formation in Light-grown and Etiolated Wheat Seedlings.

Authors:  S A Boffey; G Selldén; R M Leech
Journal:  Plant Physiol       Date:  1980-04       Impact factor: 8.340

7.  Development of Photosystem I and Photosystem II Activities in Leaves of Light-grown Maize (Zea mays).

Authors:  N R Baker; R M Leech
Journal:  Plant Physiol       Date:  1977-10       Impact factor: 8.340

8.  Organic acid and potassium accumulation in guard cells during stomatal opening.

Authors:  W H Outlaw; O H Lowry
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205

9.  Chloroplast Division and DNA Synthesis in Light-grown Wheat Leaves.

Authors:  S A Boffey; J R Ellis; G Selldén; R M Leech
Journal:  Plant Physiol       Date:  1979-09       Impact factor: 8.340

10.  Histochemical Approach to Properties of Vicia faba Guard Cell Phosphoenolpyruvate Carboxylase.

Authors:  W H Outlaw; J Manchester; C A Dicamelli
Journal:  Plant Physiol       Date:  1979-08       Impact factor: 8.340

  10 in total
  2 in total

1.  Activity of Glyceraldehyde-3-Phosphate Dehydrogenase-NADP in Developing Leaves of Light-Grown Dianthus chinensis L.

Authors:  J G Croxdale; T Pappas
Journal:  Plant Physiol       Date:  1987-08       Impact factor: 8.340

2.  The nutritional status of the apical meristem of Lactuca sativa as affected by NaCl salinization: An electron-probe microanalytic study.

Authors:  D Lazof; A Läuchli
Journal:  Planta       Date:  1991-06       Impact factor: 4.116

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.