Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.

<h4>Background</h4>Since the creation of "Golden Rice", biofortification of plant-derived foods is a promising strategy for the alleviation of nutritional deficiencies. Potato is the most important staple food for mankind after the cereals rice, wheat and maize, and is extremel...

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Main Authors: Gianfranco Diretto, Salim Al-Babili, Raffaela Tavazza, Velia Papacchioli, Peter Beyer, Giovanni Giuliano
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-04-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0000350
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spelling doaj-9beb8f577cf8483eac02271f5d7e304b2021-03-03T22:29:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032007-04-0124e35010.1371/journal.pone.0000350Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.Gianfranco DirettoSalim Al-BabiliRaffaela TavazzaVelia PapacchioliPeter BeyerGiovanni Giuliano<h4>Background</h4>Since the creation of "Golden Rice", biofortification of plant-derived foods is a promising strategy for the alleviation of nutritional deficiencies. Potato is the most important staple food for mankind after the cereals rice, wheat and maize, and is extremely poor in provitamin A carotenoids.<h4>Methodology</h4>We transformed potato with a mini-pathway of bacterial origin, driving the synthesis of beta-carotene (Provitamin A) from geranylgeranyl diphosphate. Three genes, encoding phytoene synthase (CrtB), phytoene desaturase (CrtI) and lycopene beta-cyclase (CrtY) from Erwinia, under tuber-specific or constitutive promoter control, were used. 86 independent transgenic lines, containing six different promoter/gene combinations, were produced and analyzed. Extensive regulatory effects on the expression of endogenous genes for carotenoid biosynthesis are observed in transgenic lines. Constitutive expression of the CrtY and/or CrtI genes interferes with the establishment of transgenosis and with the accumulation of leaf carotenoids. Expression of all three genes, under tuber-specific promoter control, results in tubers with a deep yellow ("golden") phenotype without any adverse leaf phenotypes. In these tubers, carotenoids increase approx. 20-fold, to 114 mcg/g dry weight and beta-carotene 3600-fold, to 47 mcg/g dry weight.<h4>Conclusions</h4>This is the highest carotenoid and beta-carotene content reported for biofortified potato as well as for any of the four major staple foods (the next best event being "Golden Rice 2", with 31 mcg/g dry weight beta-carotene). Assuming a beta-carotene to retinol conversion of 6ratio1, this is sufficient to provide 50% of the Recommended Daily Allowance of Vitamin A with 250 gms (fresh weight) of "golden" potatoes.https://doi.org/10.1371/journal.pone.0000350
collection DOAJ
language English
format Article
sources DOAJ
author Gianfranco Diretto
Salim Al-Babili
Raffaela Tavazza
Velia Papacchioli
Peter Beyer
Giovanni Giuliano
spellingShingle Gianfranco Diretto
Salim Al-Babili
Raffaela Tavazza
Velia Papacchioli
Peter Beyer
Giovanni Giuliano
Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
PLoS ONE
author_facet Gianfranco Diretto
Salim Al-Babili
Raffaela Tavazza
Velia Papacchioli
Peter Beyer
Giovanni Giuliano
author_sort Gianfranco Diretto
title Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
title_short Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
title_full Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
title_fullStr Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
title_full_unstemmed Metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
title_sort metabolic engineering of potato carotenoid content through tuber-specific overexpression of a bacterial mini-pathway.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2007-04-01
description <h4>Background</h4>Since the creation of "Golden Rice", biofortification of plant-derived foods is a promising strategy for the alleviation of nutritional deficiencies. Potato is the most important staple food for mankind after the cereals rice, wheat and maize, and is extremely poor in provitamin A carotenoids.<h4>Methodology</h4>We transformed potato with a mini-pathway of bacterial origin, driving the synthesis of beta-carotene (Provitamin A) from geranylgeranyl diphosphate. Three genes, encoding phytoene synthase (CrtB), phytoene desaturase (CrtI) and lycopene beta-cyclase (CrtY) from Erwinia, under tuber-specific or constitutive promoter control, were used. 86 independent transgenic lines, containing six different promoter/gene combinations, were produced and analyzed. Extensive regulatory effects on the expression of endogenous genes for carotenoid biosynthesis are observed in transgenic lines. Constitutive expression of the CrtY and/or CrtI genes interferes with the establishment of transgenosis and with the accumulation of leaf carotenoids. Expression of all three genes, under tuber-specific promoter control, results in tubers with a deep yellow ("golden") phenotype without any adverse leaf phenotypes. In these tubers, carotenoids increase approx. 20-fold, to 114 mcg/g dry weight and beta-carotene 3600-fold, to 47 mcg/g dry weight.<h4>Conclusions</h4>This is the highest carotenoid and beta-carotene content reported for biofortified potato as well as for any of the four major staple foods (the next best event being "Golden Rice 2", with 31 mcg/g dry weight beta-carotene). Assuming a beta-carotene to retinol conversion of 6ratio1, this is sufficient to provide 50% of the Recommended Daily Allowance of Vitamin A with 250 gms (fresh weight) of "golden" potatoes.
url https://doi.org/10.1371/journal.pone.0000350
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