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. 1994 Aug;105(4):1335–1345. doi: 10.1104/pp.105.4.1335

Metabolism of the Raffinose Family Oligosaccharides in Leaves of Ajuga reptans L. (Cold Acclimation, Translocation, and Sink to Source Transition: Discovery of Chain Elongation Enzyme).

M Bachmann 1, P Matile 1, F Keller 1
PMCID: PMC159466  PMID: 12232288

Abstract

Ajuga reptans is a frost-hardy, perennial labiate that is known for its high content of raffinose family oligosaccharide(s) (RFO). Seasonal variations in soluble nonstructural carbohydrate levels in above-ground parts of Ajuga showed that the RFO were by far the most predominant components throughout the whole year. RFO were lowest in summer (75 mg/g fresh weight) and highest in fall/winter (200 mg/g fresh weight), whereas sucrose and starch were only minor components. Cold treatment (14 d at 10/3[deg]C, day/night) of plants that were precultivated under warm conditions (25[deg]C) lowered the temperature optimum of net photosynthesis from 16[deg] to 8[deg]C, decreased the maximum rate, and increased the total nonstructural carbohydrate content of leaves by a factor of about 10, mainly because of an increase of RFO. The degree of polymerization of the RFO increased sequentially up to at least 15. A novel, galactinol-independent galactosyltransferase enzyme was found, forming from two molecules of RFO, the next higher and lower degree of polymerization of RFO. The enzyme had a pH optimum of 4.5 to 5.0 and may be responsible for RFO chain elongation. RFO were the main carbohydrates translocated in the phloem, with stachyose being by far the most dominant form. Studies of carbon balance during leaf development revealed a transition point between import and export at approximately 25% maximal leaf area. RFO synthesis could be detected even before the commencement of export, suggesting the existence of a nonphloem-linked RFO pool even in very young leaves. Taken together, it seems that Ajuga leaves contain two pools of RFO metabolism, a pronounced long-term storage pool in the mesophyll, possibly also involved in frost resistance, and a transport pool in the phloem.

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Selected References

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  1. Bourne E. J., Walter M. W., Pridham J. B. The biosynthesis of raffinose. Biochem J. 1965 Dec;97(3):802–806. doi: 10.1042/bj0970802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Dey P. M., Pridham J. B. Biochemistry of -galactosidases. Adv Enzymol Relat Areas Mol Biol. 1972;36:91–130. doi: 10.1002/9780470122815.ch3. [DOI] [PubMed] [Google Scholar]
  3. Giaquinta R. Source and sink leaf metabolism in relation to Phloem translocation: carbon partitioning and enzymology. Plant Physiol. 1978 Mar;61(3):380–385. doi: 10.1104/pp.61.3.380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. HERISSEY H., FLEURY P., WICKSTROM A., COURTOIS J. E., LE DIZET P. Isolement de cin galactosides du saccharose des racines de bouillon blanc. Bull Soc Chim Biol (Paris) 1954;36(11-12):1507–1518. [PubMed] [Google Scholar]
  5. Helmerhorst E., Stokes G. B. Microcentrifuge desalting: a rapid, quantitative method for desalting small amounts of protein. Anal Biochem. 1980 May 1;104(1):130–135. doi: 10.1016/0003-2697(80)90287-0. [DOI] [PubMed] [Google Scholar]
  6. Herman E. M., Shannon L. M. Accumulation and Subcellular Localization of alpha-Galactosidase-Hemagglutinin in Developing Soybean Cotyledons. Plant Physiol. 1985 Apr;77(4):886–890. doi: 10.1104/pp.77.4.886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hubbard N. L., Huber S. C., Pharr D. M. Sucrose Phosphate Synthase and Acid Invertase as Determinants of Sucrose Concentration in Developing Muskmelon (Cucumis melo L.) Fruits. Plant Physiol. 1989 Dec;91(4):1527–1534. doi: 10.1104/pp.91.4.1527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Huber S. C., Huber J. L. Role of sucrose-phosphate synthase in sucrose metabolism in leaves. Plant Physiol. 1992 Aug;99(4):1275–1278. doi: 10.1104/pp.99.4.1275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. King R. W., Zeevaart J. A. Enhancement of Phloem exudation from cut petioles by chelating agents. Plant Physiol. 1974 Jan;53(1):96–103. doi: 10.1104/pp.53.1.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mitchell D. E., Madore M. A. Patterns of Assimilate Production and Translocation in Muskmelon (Cucumis melo L.) : II. Low Temperature Effects. Plant Physiol. 1992 Jul;99(3):966–971. doi: 10.1104/pp.99.3.966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Smith P. T., Kuo T. M., Crawford C. G. Purification and characterization of galactinol synthase from mature zucchini squash leaves. Plant Physiol. 1991 Jul;96(3):693–698. doi: 10.1104/pp.96.3.693. [DOI] [PMC free article] [PubMed] [Google Scholar]

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