Your browser doesn't support javascript.
loading
Diterpenoid fingerprints in pine foliage across an environmental and chemotypic matrix: Isoabienol content is a key trait differentiating chemotypes.
Kännaste, Astrid; Laanisto, Lauri; Pazouki, Leila; Copolovici, Lucian; Suhorutsenko, Marina; Azeem, Muhammad; Toom, Lauri; Borg-Karlson, Anna-Karin; Niinemets, Ülo.
Afiliação
  • Kännaste A; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia. Electronic address: astrid.kannaste@emu.ee.
  • Laanisto L; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia. Electronic address: lauri.laanisto@emu.ee.
  • Pazouki L; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Department of Biology, University of Louisville, Louisville, KY 40292, USA. Electronic address: leila.pazouki@emu.ee.
  • Copolovici L; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Institute of Technical and Natural Sciences Research-Development of "Aurel Vlaicu" University, 2 Elena Dragoi St., Arad 310330, Romania. Electronic address: lucian.copolov
  • Suhorutsenko M; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia. Electronic address: marina.suhorutsenko@ut.ee.
  • Azeem M; Department of Chemistry, COMSATS Institute of Information Technology, Abbottabad 22060, Pakistan; Ecological Chemistry Group, Department of Chemistry, KTH, Royal Institute of Technology, 100 44 Stockholm, Sweden. Electronic address: mazeemfsd@hotmail.com.
  • Toom L; Institute of Technology, University of Tartu, Nooruse 1, Tartu 50411, Estonia. Electronic address: lauri.toom@ut.ee.
  • Borg-Karlson AK; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Ecological Chemistry Group, Department of Chemistry, KTH, Royal Institute of Technology, 100 44 Stockholm, Sweden; Institute of Technology, University of Tartu, Nooruse 1,
  • Niinemets Ü; Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Estonian Academy of Sciences, Kohtu 6, 10130 Tallinn, Estonia. Electronic address: ylo.niinemets@emu.ee.
Phytochemistry ; 147: 80-88, 2018 Mar.
Article em En | MEDLINE | ID: mdl-29304384
ABSTRACT
Diterpenoids constitute an important part of oleoresin in conifer needles, but the environmental and genetic controls on diterpenoid composition are poorly known. We studied the presence of diterpenoids in four pine populations spanning an extensive range of nitrogen (N) availability. In most samples, isoabienol was the main diterpenoid. Additionally, low contents of (Z)-biformene, abietadiene isomers, manoyl oxide isomers, labda-7,13,14-triene and labda-7,14-dien-13-ol were quantified in pine needles. According to the occurrence and content of diterpenoids it was possible to distinguish 'non diterpenoid pines', 'high isoabienol pines', 'manoyl oxide - isoabienol pines' and 'other diterpenoid pines'. 'Non diterpenoid pines', 'high isoabienol pines' and 'other diterpenoid pines' were characteristic to the dry forest, yet the majority of pines (>80%) of the bog Laeva represented 'high isoabienol pines'. 'Manoyl oxide - isoabienol pines' were present only in the wet sites. Additionally, orthogonal partial least-squares analysis showed, that in the bogs foliar nitrogen content per dry mass (NM) correlated to diterpenoids. Significant correlations existed between abietadienes, isoabienol and foliar NM in 'manoyl oxide - isoabienol pines', and chemotypic variation was also associated by population genetic distance estimated by nuclear microsatellite markers. Previously, the presence of low and high Δ-3-carene pines has been demonstrated, but the results of the current study indicate that also diterpenoids form an independent axis of chemotypic differentiation. Further studies are needed to understand whether the enhanced abundance of diterpenoids in wetter sites reflects a phenotypic or genotypic response.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pinus / Diterpenos / Naftóis Idioma: En Revista: Phytochemistry Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pinus / Diterpenos / Naftóis Idioma: En Revista: Phytochemistry Ano de publicação: 2018 Tipo de documento: Article