» Articles » PMID: 15122035

Evidence for Apoplasmic Phloem Unloading in Developing Apple Fruit

Overview
Journal Plant Physiol
Specialty Physiology
Date 2004 May 4
PMID 15122035
Citations 72
Authors
Affiliations
Soon will be listed here.
Abstract

The phloem unloading pathway remains unclear in fleshy fruits accumulating a high level of soluble sugars. A structural investigation in apple fruit (Malus domestica Borkh. cv Golden Delicious) showed that the sieve element-companion cell complex of the sepal bundles feeding the fruit flesh is symplasmically isolated over fruit development. 14C-autoradiography indicated that the phloem of the sepal bundles was functional for unloading. Confocal laser scanning microscopy imaging of carboxyfluorescein unloading showed that the dye remained confined to the phloem strands of the sepal bundles from the basal to the apical region of the fruit. A 52-kD putative monosaccharide transporter was immunolocalized predominantly in the plasma membrane of both the sieve elements and parenchyma cells and its amount increased during fruit development. A 90-kD plasma membrane H(+)-ATPase was also localized in the plasma membrane of the sieve element-companion cell complex. Studies of [14C]sorbitol unloading suggested that an energy-driven monosaccharide transporter may be functional in phloem unloading. These data provide clear evidence for an apoplasmic phloem unloading pathway in apple fruit and give information on the structural and molecular features involved in this process.

Citing Articles

Significance of Raffinose Family Oligosaccharides (RFOs) metabolism in plants.

Liu H, Wang F, Liu B, Kong F, Fang C Adv Biotechnol (Singap). 2025; 2(2):13.

PMID: 39883346 PMC: 11740855. DOI: 10.1007/s44307-024-00022-y.


Comparison of antioxidant, phenolic profile, melatonin, and volatile compounds of some selected plant samples.

Binici H, Sat I, Yilmaz B Food Sci Nutr. 2024; 12(10):7158-7165.

PMID: 39479601 PMC: 11521718. DOI: 10.1002/fsn3.4334.


Source-sink synergy is the key unlocking sweet potato starch yield potential.

Jiang Z, Wei Z, Zhang J, Zheng C, Zhu H, Zhai H Nat Commun. 2024; 15(1):7260.

PMID: 39179563 PMC: 11343742. DOI: 10.1038/s41467-024-51727-6.


Sugar import mediated by sugar transporters and cell wall invertases for seed development in .

Du B, Cao Y, Zhou J, Chen Y, Ye Z, Huang Y Hortic Res. 2024; 11(7):uhae133.

PMID: 38974190 PMC: 11226869. DOI: 10.1093/hr/uhae133.


Sugar delivery at the tomato root and root galls after Meloidogyne incognita infestation.

Sun L, Lian L, Yang R, Li T, Yang M, Zhao W BMC Plant Biol. 2024; 24(1):451.

PMID: 38789940 PMC: 11119304. DOI: 10.1186/s12870-024-05157-7.


References
1.
Oparka K . What is Phloem unloading?. Plant Physiol. 1990; 94(2):393-6. PMC: 1077243. DOI: 10.1104/pp.94.2.393. View

2.
Viola R, Roberts A, Haupt S, Gazzani S, Hancock R, Marmiroli N . Tuberization in potato involves a switch from apoplastic to symplastic phloem unloading. Plant Cell. 2001; 13(2):385-98. PMC: 102249. DOI: 10.1105/tpc.13.2.385. View

3.
Sonnewald U, Hajirezaei M, Kossmann J, Heyer A, Trethewey R, Willmitzer L . Increased potato tuber size resulting from apoplastic expression of a yeast invertase. Nat Biotechnol. 1997; 15(8):794-7. DOI: 10.1038/nbt0897-794. View

4.
Itaya A, Ma F, Qi Y, Matsuda Y, Zhu Y, Liang G . Plasmodesma-mediated selective protein traffic between "symplasmically isolated" cells probed by a viral movement protein. Plant Cell. 2002; 14(9):2071-83. PMC: 150756. DOI: 10.1105/tpc.003954. View

5.
van Bel A . Interaction between sieve element and companion cell and the consequences for photoassimilate distribution. Two structural hardware frames with associated physiological software packages in dicotyledons?. J Exp Bot. 2011; 47 Spec No:1129-40. DOI: 10.1093/jxb/47.Special_Issue.1129. View