Radiosynthesis of 6'-Deoxy-6'[18F]Fluorosucrose via Automated Synthesis and Its Utility to Study In Vivo Sucrose Transport in Maize (Zea mays) Leaves

Sugars produced from photosynthesis in leaves are transported through the phloem tissues within veins and delivered to non-photosynthetic organs, such as roots, stems, flowers, and seeds, to support their growth and/or storage of carbohydrates. However, because the phloem is located internally withi...

Full description

Saved in:
Bibliographic Details
Published inPloS one Vol. 10; no. 5; p. e0128989
Main Authors Rotsch, David, Brossard, Tom, Bihmidine, Saadia, Ying, Weijiang, Gaddam, Vikram, Harmata, Michael, Robertson, J David, Swyers, Michael, Jurisson, Silvia S, Braun, David M
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 29.05.2015
Public Library of Science (PLoS)
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Sugars produced from photosynthesis in leaves are transported through the phloem tissues within veins and delivered to non-photosynthetic organs, such as roots, stems, flowers, and seeds, to support their growth and/or storage of carbohydrates. However, because the phloem is located internally within the veins, it is difficult to access and to study the dynamics of sugar transport. Radioactive tracers have been extensively used to study vascular transport in plants and have provided great insights into transport dynamics. To better study sucrose partitioning in vivo, a novel radioactive analog of sucrose was synthesized through a completely chemical synthesis route by substituting fluorine-18 (half-life 110 min) at the 6' position to generate 6'-deoxy-6'[(18)F]fluorosucrose ((18)FS). This radiotracer was then used to compare sucrose transport between wild-type maize plants and mutant plants lacking the Sucrose transporter1 (Sut1) gene, which has been shown to function in sucrose phloem loading. Our results demonstrate that (18)FS is transported in vivo, with the wild-type plants showing a greater rate of transport down the leaf blade than the sut1 mutant plants. A similar transport pattern was also observed for universally labeled [U-(14)C]sucrose ([U-(14)C]suc). Our findings support the proposed sucrose phloem loading function of the Sut1 gene in maize, and additionally demonstrate that the (18)FS analog is a valuable, new tool that offers imaging advantages over [U-(14)C]suc for studying phloem transport in plants.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
SC0002040; SC0006810; IOS–1025976; IIA-1430428
USDOE Office of Science (SC)
National Science Foundation (NSF)
Competing Interests: The authors have declared that no competing interests exist.
Current address: Department of Pathology, University of Michigan, Ann Arbor, Michigan, United States of America
Current address: Argonne National Laboratory, Argonne, Illinois, United States of America
Current address: School of Chemistry, University of Hyderabad, Hyderabad, India
Conceived and designed the experiments: DR TB SB WY VG MH JDR SJ DMB. Performed the experiments: DR TB SB WY VG MS. Analyzed the data: DR TB SB MH JDR MS SJ DMB. Contributed reagents/materials/analysis tools: DR TB SB WY VG MH JDR MS SJ DMB. Wrote the paper: DR TB SB MH JDR SJ DMB.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0128989