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Fungal endophytes of Catharanthus roseus enhance vindoline content by modulating structural and regulatory genes related to terpenoid indole alkaloid biosynthesis

Identifieur interne : 000208 ( Main/Exploration ); précédent : 000207; suivant : 000209

Fungal endophytes of Catharanthus roseus enhance vindoline content by modulating structural and regulatory genes related to terpenoid indole alkaloid biosynthesis

Auteurs : Shiv S. Pandey [Inde] ; Sucheta Singh [Inde] ; C. S. Vivek Babu ; Karuna Shanker [Inde] ; N. K. Srivastava [Inde] ; Ashutosh K. Shukla [Inde] ; Alok Kalra [Inde]

Source :

RBID : PMC:4879578

Abstract

Not much is known about the mechanism of endophyte-mediated induction of secondary metabolite production in Catharanthus roseus. In the present study two fungal endophytes, Curvularia sp. CATDLF5 and Choanephora infundibulifera CATDLF6 were isolated from the leaves of the plant that were found to enhance vindoline content by 229–403%. The isolated endophytes did not affect the primary metabolism of the plant as the maximum quantum efficiency of PSII, net CO2 assimilation, plant biomass and starch content of endophyte-inoculated plants was similar to endophyte-free control plants. Expression of terpenoid indole alkaloid (TIA) pathway genes, geraniol 10-hydroxylase (G10H), tryptophan decarboxylase (TDC), strictosidine synthase (STR), 16-hydoxytabersonine-O-methyltransferase (16OMT), desacetoxyvindoline-4-hydroxylase (D4H), deacetylvindoline-4-O-acetyltransferase (DAT) were upregulated in endophyte-inoculated plants. Endophyte inoculation upregulated the expression of the gene for transcriptional activator octadecanoid-responsive Catharanthus AP2-domain protein (ORCA3) and downregulated the expression of Cys2/His2-type zinc finger protein family transcriptional repressors (ZCTs). The gene for the vacuolar class III peroxidase (PRX1), responsible for coupling vindoline and catharanthine, was upregulated in endophyte-inoculated plants. These endophytes may enhance vindoline production by modulating the expression of key structural and regulatory genes of vindoline biosynthesis without affecting the primary metabolism of the host plant.


Url:
DOI: 10.1038/srep26583
PubMed: 27220774
PubMed Central: 4879578


Affiliations:


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Le document en format XML

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<p>Not much is known about the mechanism of endophyte-mediated induction of secondary metabolite production in
<italic>Catharanthus roseus</italic>
. In the present study two fungal endophytes,
<italic>Curvularia</italic>
sp. CATDLF5 and
<italic>Choanephora infundibulifera</italic>
CATDLF6 were isolated from the leaves of the plant that were found to enhance vindoline content by 229–403%. The isolated endophytes did not affect the primary metabolism of the plant as the maximum quantum efficiency of PSII, net CO
<sub>2</sub>
assimilation, plant biomass and starch content of endophyte-inoculated plants was similar to endophyte-free control plants. Expression of terpenoid indole alkaloid (TIA) pathway genes, geraniol 10-hydroxylase (
<italic>G10H</italic>
), tryptophan decarboxylase (
<italic>TDC</italic>
), strictosidine synthase (
<italic>STR</italic>
), 16-hydoxytabersonine-
<italic>O</italic>
-methyltransferase (
<italic>16OMT</italic>
), desacetoxyvindoline-4-hydroxylase (
<italic>D4H</italic>
), deacetylvindoline-4-
<italic>O</italic>
-acetyltransferase (
<italic>DAT</italic>
) were upregulated in endophyte-inoculated plants. Endophyte inoculation upregulated the expression of the gene for transcriptional activator octadecanoid-responsive Catharanthus AP2-domain protein (
<italic>ORCA3</italic>
) and downregulated the expression of Cys2/His2-type zinc finger protein family transcriptional repressors (
<italic>ZCTs</italic>
). The gene for the vacuolar class III peroxidase (
<italic>PRX1</italic>
), responsible for coupling vindoline and catharanthine, was upregulated in endophyte-inoculated plants. These endophytes may enhance vindoline production by modulating the expression of key structural and regulatory genes of vindoline biosynthesis without affecting the primary metabolism of the host plant.</p>
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