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. 1992 Nov;100(3):1238–1242. doi: 10.1104/pp.100.3.1238

Regulation of Sucrose Phosphate Synthase by Gibberellins in Soybean and Spinach Plants 1

Nordine Cheikh 1,2,3,4,2, Mark L Brenner 1,2,3,4, Joan L Huber 1,2,3,4, Steven C Huber 1,2,3,4
PMCID: PMC1075772  PMID: 16653111

Abstract

Exogenous applications of gibberellins (GAs) increased the extractable activity of leaf sucrose phosphate synthase (SPS) in soybean (Glycine max [L.]) and spinach (Spinacia oleracea [L.]). The response to GA applications was detectable within 2 h postapplication and was still observed 6 h, 24 h, and 7 d after treatment. When paclobutrazol, a GA biosynthesis inhibitor, was applied to intact soybean and spinach plants, decreased extractable SPS activity resulted within 24 h following the treatment. Different methods of GA application (spray, injection, capillary wick, and excised leaf systems) produced similar effects on SPS activity of soybean leaves. Protein synthesis in soybean leaves appeared to be necessary for GA-promoted SPS activity because gibberellic acid only partially reversed the inhibitory effect of pretreatment with cycloheximide. Levels of SPS protein from crude extracts of spinach plants were measured by a dot blot technique using monoclonal antibodies against SPS. Application of gibberellic acid to spinach leaves increased levels of SPS protein 2 h, 24 h, and 7 d after treatment. The results suggest that, in both soybean and spinach, GA is one of the endogenous hormonal factors that regulate the steady-state level of SPS protein and, hence, its activity.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Huber J. L., Huber S. C., Nielsen T. H. Protein phosphorylation as a mechanism for regulation of spinach leaf sucrose-phosphate synthase activity. Arch Biochem Biophys. 1989 May 1;270(2):681–690. doi: 10.1016/0003-9861(89)90551-1. [DOI] [PubMed] [Google Scholar]
  2. Kaufman P. B., Ghosheh N., Ikuma H. Promotion of growth and invertase activity by gibberellic Acid in developing Avena internodes. Plant Physiol. 1968 Jan;43(1):29–34. doi: 10.1104/pp.43.1.29. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Kerr P. S., Huber S. C., Israel D. W. Effect of N-source on soybean leaf sucrose phosphate synthase, starch formation, and whole plant growth. Plant Physiol. 1984 Jun;75(2):483–488. doi: 10.1104/pp.75.2.483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Kerr P. S., Rufty T. W., Huber S. C. Endogenous Rhythms in Photosynthesis, Sucrose Phosphate Synthase Activity, and Stomatal Resistance in Leaves of Soybean (Glycine max [L.] Merr.). Plant Physiol. 1985 Feb;77(2):275–280. doi: 10.1104/pp.77.2.275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Sicher R. C., Kremer D. F. Changes of Sucrose-Phosphate Synthase Activity in Barley Primary Leaves during Light/Dark Transitions. Plant Physiol. 1984 Dec;76(4):910–912. doi: 10.1104/pp.76.4.910. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Sicher R. C., Kremer D. F. Possible control of maize leaf sucrose-phosphate synthase activity by light modulation. Plant Physiol. 1985 Nov;79(3):695–698. doi: 10.1104/pp.79.3.695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Varner J. E. Gibberellic Acid Controlled Synthesis of alpha-Amylase in Barley Endosperm. Plant Physiol. 1964 May;39(3):413–415. doi: 10.1104/pp.39.3.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Walker J. L., Huber S. C. Purification and preliminary characterization of sucrose-phosphate synthase using monoclonal antibodies. Plant Physiol. 1989 Feb;89(2):518–524. doi: 10.1104/pp.89.2.518. [DOI] [PMC free article] [PubMed] [Google Scholar]

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