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PMID: 16659124 Published · ppublish English Journal Article

Determination of structure and composition of suberin from the roots of carrot, parsnip, rutabaga, turnip, red beet, and sweet potato by combined gas-liquid chromatography and mass spectrometry.

Plant physiology ·Vol. 55 ·No. 3 ·1975-03-00 ·Pages 567-73

Kolattukudy PE, Kronman K, Poulose AJ

Abstract

Suberin from the roots of carrots (Daucus carota), parsnip (Pastinaca sativa), rutabaga (Brassica napobrassica), turnip (Brassica rapa), red beet (Beta vulgaris), and sweet potato (Ipomoea batatas) was isolated by a combination of chemical and enzymatic techniques. Finely powdered suberin was depolymerized with 14% BF(3) in methanol, and soluble monomers (20-50% of suberin) were fractionated into phenolic (<10%) and aliphatic (13-35%) fractions. The aliphatic fractions consisted mainly of omega-hydroxyacids (29-43%), dicarboxylic acids (16-27%), fatty acids (4-18%), and fatty alcohols (3-6%). Each fraction was subjected to combined gas-liquid chromatography and mass spectrometry. Among the fatty acids very long chain acids (>C(20)) were the dominant components in all six plants. In the alcohol fraction C(18), C(20), C(22), and C(24) saturated primary alcohols were the major components. C(16) and C(18) dicarboxylic acids were the major dicarboxylic acids of the suberin of all six plants and in all cases octadec-9-ene-1, 18-dioic acid was the major component except in rutabaga where hexadecane-1, 16-dioic acid was the major dicarboxylic acid. The composition of the omega-hydroxyacid fraction was quite similar to that of the dicarboxylic acids; 18-hydroxy-octadec-9-enoic acid was the major component in all plants except rutabaga, where equal quantities of 16-hydroxyhexadecanoic acid and 18-hydroxyoctadec-9-enoic acid (42% each) were found. Compounds which would be derived from 18-hydroxyoctadec-9-enoic acid and octadec-9-ene-1, 18-dioic acid by epoxidation, and epoxidation followed by hydration of the epoxide, were also detected in most of the suberin samples. The monomer composition of the six plants showed general similarities but quite clear taxonomic differences.

Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kolattukudy P E
Department of Agricultural Chemistry and Program in Biochemistry and Biophysics, Washington State University, Pullman, Washington 99163.
Kronman K
Poulose A J
References (3)
3 references, click to expand
  1. The biochemistry of plant cuticular lipids.
    Prog Chem Fats Other Lipids. 1972;13(3):119-75 PMID: 4602868
  2. Determination of the structures of cutin monomers by a novel depolymerization procedure and combined gas chromatography and mass spectrometry.
    Biochemistry. 1972 May 9;11(10):1885-96 PMID: 5025631
  3. Structure and biosynthesis of the hydroxy fatty acids of cutin in Vicia faba leaves.
    Biochemistry. 1972 May 9;11(10):1897-907 PMID: 5025632
Article Info
Journal
Plant physiology
Abbr.
Plant Physiol
ISSN
0032-0889
Published
1975-03-00
Pages
567-73
Language
English
Region
United States
NLM ID
0401224
PMCID
PMC541660
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