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. 1997 May;114(1):153–160. doi: 10.1104/pp.114.1.153

Carbohydrate Content and Enzyme Metabolism in Developing Canola Siliques.

S P King 1, J E Lunn 1, R T Furbank 1
PMCID: PMC158289  PMID: 12223695

Abstract

Little biochemical information is available on carbohydrate metabolism in developing canola (Brassica napus L.) silique (pod) wall and seed tissues. This research examines the carbohydrate contents and sucrose (Suc) metabolic enzyme activities in different aged silique wall and seed tissues during oil filling. The silique wall partitioned photosynthate into Suc over starch and predominantly accumulated hexose. The silique wall hexose content and soluble acid invertase activity rapidly fell as embryos progressed from the early- to late-cotyledon developmental stages. A similar trend was not evident for alkaline invertase, Suc synthase (SuSy), and Suc-phosphate synthase. Silique wall SuSy activities were much higher than source leaves at all times and may serve to supply the substrate for secondary cell wall thickening. In young seeds starch was the predominant accumulated carbohydrate over the sampled developmental range. Seed hexose levels dropped as embryos developed from the early- to midcotyledon stage. Hexose and starch were localized to the testa or liquid endosperm, whereas Suc was evenly distributed among seed components. With the switch to oil accumulation, seed SuSy activity increased by 3.6-fold and soluble acid invertase activity decreased by 76%. These data provide valuable baseline knowledge for the genetic manipulation of canola seed carbon partitioning.

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Selected References

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

  1. Chourey P. S., Nelson O. E. The enzymatic deficiency conditioned by the shrunken-1 mutations in maize. Biochem Genet. 1976 Dec;14(11-12):1041–1055. doi: 10.1007/BF00485135. [DOI] [PubMed] [Google Scholar]
  2. Heim U., Weber H., Bäumlein H., Wobus U. A sucrose-synthase gene of Vicia faba L.: expression pattern in developing seeds in relation to starch synthesis and metabolic regulation. Planta. 1993;191(3):394–401. doi: 10.1007/BF00195698. [DOI] [PubMed] [Google Scholar]
  3. Ross H. A., McRae D., Davies H. V. Sucrolytic Enzyme Activities in Cotyledons of the Faba Bean (Developmental Changes and Purification of Alkaline Invertase). Plant Physiol. 1996 May;111(1):329–338. doi: 10.1104/pp.111.1.329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Sung S. J., Xu D. P., Black C. C. Identification of actively filling sucrose sinks. Plant Physiol. 1989 Apr;89(4):1117–1121. doi: 10.1104/pp.89.4.1117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Vijayagopal P., Figueroa J. E., Fontenot J. D., Glancy D. L. Isolation and characterization of a proteoglycan variant from human aorta exhibiting a marked affinity for low density lipoprotein and demonstration of its enhanced expression in atherosclerotic plaques. Atherosclerosis. 1996 Dec 20;127(2):195–203. doi: 10.1016/s0021-9150(96)05954-0. [DOI] [PubMed] [Google Scholar]
  6. Weber H., Borisjuk L., Heim U., Buchner P., Wobus U. Seed coat-associated invertases of fava bean control both unloading and storage functions: cloning of cDNAs and cell type-specific expression. Plant Cell. 1995 Nov;7(11):1835–1846. doi: 10.1105/tpc.7.11.1835. [DOI] [PMC free article] [PubMed] [Google Scholar]

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