Leaf cuticle analyses: Implications for the existence of cutan/non-ester cutin and its biosynthetic origin

The cuticle of a limited number of plant species contains cutan, a chemically highly resistant biopolymer. As yet, the biosynthesis of cutan is not fully understood. Attempting to further unravel the origin of cutan, we analysed the chemical composition of enzymatically isolated cuticular membranes...

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Published in:Annals of botany Vol. 126; no. 1; pp. 141 - 162
Main Authors: Leide, Jana, Nierop, Klaas G J, Deininger, Ann-Christin, Staiger, Simona, Riederer, Markus, de Leeuw, Jan W
Format: Journal Article
Language:English
Published: England Oxford University Press 19-06-2020
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Abstract The cuticle of a limited number of plant species contains cutan, a chemically highly resistant biopolymer. As yet, the biosynthesis of cutan is not fully understood. Attempting to further unravel the origin of cutan, we analysed the chemical composition of enzymatically isolated cuticular membranes of Agave americana leaves. Cuticular waxes were extracted with organic solvents. Subsequently, the dewaxed cuticular membrane was depolymerised by acid-catalysed transesterification yielding cutin monomers and cutan, a non-hydrolysable, cuticular membrane residue. The cutan matrix was analysed by thermal extraction, flash pyrolysis and THM to elucidate the monomeric composition and deducing a putative biosynthetic origin. According to gas chromatography-mass spectrometry analyses, the cuticular waxes of A. americana contained primarily very-long-chain alkanoic acids and primary alkanols dominated by C32, whereas the cutin biopolyester of A. americana mainly consisted of 9,10-epoxy ω-hydroxy and 9,10,ω-trihydroxy C18 alkanoic acids. The main aliphatic cutan monomers were alkanoic acids, primary alkanols, ω-hydroxy alkanoic acids and alkane-α,ω-diols ranging predominantly from C28 to C34 and maximizing at C32. Minor contributions of benzene-1,3,5-triol and derivatives suggested that these aromatic moieties form the polymeric core of cutan, to which the aliphatic moieties are linked via ester and possibly ether bonds. High similarity of aliphatic moieties in the cutan and the cuticular wax component indicated a common biosynthetic origin. In order to exclude species-specific peculiarities of A. americana and to place our results in a broader context, cuticular waxes, cutin and cutan of Clivia miniata, Ficus elastica and Prunus laurocerasus leaves were investigated, too. A detailed comparison showed compositional and structural differences and pointed out that cutan was only found in leaves of perennial evergreen A. americana and C. miniata and made clear that the phenomenon of cutan is possibly less present in plant species than suggested in the literature.
AbstractList The cuticle of a limited number of plant species contains cutan, a chemically highly resistant biopolymer. As yet, the biosynthesis of cutan is not fully understood. Attempting to further unravel the origin of cutan, we analysed the chemical composition of enzymatically isolated cuticular membranes of Agave americana leaves. Cuticular waxes were extracted with organic solvents. Subsequently, the dewaxed cuticular membrane was depolymerised by acid-catalysed transesterification yielding cutin monomers and cutan, a non-hydrolysable, cuticular membrane residue. The cutan matrix was analysed by thermal extraction, flash pyrolysis and THM to elucidate the monomeric composition and deducing a putative biosynthetic origin. According to gas chromatography-mass spectrometry analyses, the cuticular waxes of A. americana contained primarily very-long-chain alkanoic acids and primary alkanols dominated by C32, whereas the cutin biopolyester of A. americana mainly consisted of 9,10-epoxy ω-hydroxy and 9,10,ω-trihydroxy C18 alkanoic acids. The main aliphatic cutan monomers were alkanoic acids, primary alkanols, ω-hydroxy alkanoic acids and alkane-α,ω-diols ranging predominantly from C28 to C34 and maximizing at C32. Minor contributions of benzene-1,3,5-triol and derivatives suggested that these aromatic moieties form the polymeric core of cutan, to which the aliphatic moieties are linked via ester and possibly ether bonds. High similarity of aliphatic moieties in the cutan and the cuticular wax component indicated a common biosynthetic origin. In order to exclude species-specific peculiarities of A. americana and to place our results in a broader context, cuticular waxes, cutin and cutan of Clivia miniata, Ficus elastica and Prunus laurocerasus leaves were investigated, too. A detailed comparison showed compositional and structural differences and pointed out that cutan was only found in leaves of perennial evergreen A. americana and C. miniata and made clear that the phenomenon of cutan is possibly less present in plant species than suggested in the literature.
BACKGROUND AND AIMSThe cuticle of a limited number of plant species contains cutan, a chemically highly resistant biopolymer. As yet, the biosynthesis of cutan is not fully understood. Attempting to further unravel the origin of cutan, we analysed the chemical composition of enzymatically isolated cuticular membranes of Agave americana leaves. METHODSCuticular waxes were extracted with organic solvents. Subsequently, the dewaxed cuticular membrane was depolymerized by acid-catalysed transesterification yielding cutin monomers and cutan, a non-hydrolysable, cuticular membrane residue. The cutan matrix was analysed by thermal extraction, flash pyrolysis and thermally assisted hydrolysis and methylation to elucidate the monomeric composition and deduce a putative biosynthetic origin. KEY RESULTSAccording to gas chromatography-mass spectrometry analyses, the cuticular waxes of A. americana contained primarily very-long-chain alkanoic acids and primary alkanols dominated by C32, whereas the cutin biopolyester of A. americana mainly consisted of 9,10-epoxy ω-hydroxy and 9,10,ω-trihydroxy C18 alkanoic acids. The main aliphatic cutan monomers were alkanoic acids, primary alkanols, ω-hydroxy alkanoic acids and alkane-α,ω-diols ranging predominantly from C28 to C34 and maximizing at C32. Minor contributions of benzene-1,3,5-triol and derivatives suggested that these aromatic moieties form the polymeric core of cutan, to which the aliphatic moieties are linked via ester and possibly ether bonds. CONCLUSIONSHigh similarity of aliphatic moieties in the cutan and the cuticular wax component indicated a common biosynthetic origin. In order to exclude species-specific peculiarities of A. americana and to place our results in a broader context, cuticular waxes, cutin and cutan of Clivia miniata, Ficus elastica and Prunus laurocerasus leaves were also investigated. A detailed comparison showed compositional and structural differences, indicated that cutan was only found in leaves of perennial evergreen A. americana and C. miniata, and made clear that the phenomenon of cutan is possibly less present in plant species than suggested in the literature.
Author Deininger, Ann-Christin
Leide, Jana
de Leeuw, Jan W
Riederer, Markus
Staiger, Simona
Nierop, Klaas G J
AuthorAffiliation 1 University of Würzburg, Julius-von-Sachs-Institute for Biosciences , Würzburg, Germany
2 Department of Earth Sciences, Faculty of Geosciences, Utrecht University , CB Utrecht, The Netherlands
3 NIOZ Royal Netherlands Institute for Sea Research , Den Burg, The Netherlands
AuthorAffiliation_xml – name: 3 NIOZ Royal Netherlands Institute for Sea Research , Den Burg, The Netherlands
– name: 2 Department of Earth Sciences, Faculty of Geosciences, Utrecht University , CB Utrecht, The Netherlands
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  surname: Nierop
  fullname: Nierop, Klaas G J
  organization: Department of Earth Sciences, Faculty of Geosciences, Utrecht University, The Netherlands
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  givenname: Ann-Christin
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Copyright The Author(s) 2020. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
The Author(s) 2020. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2020
Copyright_xml – notice: The Author(s) 2020. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
– notice: The Author(s) 2020. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2020
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Issue 1
Keywords Ficus elastica
Prunus laurocerasus
cuticular waxes
Fourier transform infrared spectroscopy (FTIR)
Clivia miniata
cutan
flash pyrolysis
cutin
Agave americana
non-ester cutin
thermally assisted hydrolysis and methylation (THM)
Language English
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Snippet The cuticle of a limited number of plant species contains cutan, a chemically highly resistant biopolymer. As yet, the biosynthesis of cutan is not fully...
BACKGROUND AND AIMSThe cuticle of a limited number of plant species contains cutan, a chemically highly resistant biopolymer. As yet, the biosynthesis of cutan...
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StartPage 141
SubjectTerms Original
Title Leaf cuticle analyses: Implications for the existence of cutan/non-ester cutin and its biosynthetic origin
URI https://www.ncbi.nlm.nih.gov/pubmed/32222770
https://search.proquest.com/docview/2384494512
https://pubmed.ncbi.nlm.nih.gov/PMC7304474
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