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1.
J Exp Bot ; 62(14): 4975-93, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21778185

ABSTRACT

Oilseed rape and other crop plants of the family Brassicaceae contain a unique defence system known as the glucosinolate-myrosinase system or the 'mustard oil bomb'. The 'mustard oil bomb' which includes myrosinase and glucosinolates is triggered by abiotic and biotic stress, resulting in the formation of toxic products such as nitriles and isothiocyanates. Myrosinase is present in specialist cells known as 'myrosin cells' and can also be known as toxic mines. The myrosin cell idioblasts of Brassica napus were genetically reprogrammed to undergo controlled cell death (ablation) during seed development. These myrosin cell-free plants have been named MINELESS as they lack toxic mines. This has led to the production of oilseed rape with a significant reduction both in myrosinase levels and in the hydrolysis of glucosinolates. Even though the myrosinase activity in MINELESS was very low compared with the wild type, variation was observed. This variability was overcome by producing homozygous seeds. A microspore culture technique involving non-fertile haploid MINELESS plants was developed and these plants were treated with colchicine to produce double haploid MINELESS plants with full fertility. Double haploid MINELESS plants had significantly reduced myrosinase levels and glucosinolate hydrolysis products. Wild-type and MINELESS plants exhibited significant differences in growth parameters such as plant height, leaf traits, matter accumulation, and yield parameters. The growth and developmental pattern of MINELESS plants was relatively slow compared with the wild type. The characteristics of the pure double haploid MINELESS plant are described and its importance for future biochemical, agricultural, dietary, functional genomics, and plant defence studies is discussed.


Subject(s)
Brassica napus/enzymology , Glucosinolates/metabolism , Glycoside Hydrolases/metabolism , Plant Proteins/metabolism , Plants, Genetically Modified/enzymology , Seeds/genetics , Brassica napus/cytology , Brassica napus/genetics , Brassica napus/metabolism , Glycoside Hydrolases/genetics , Haploidy , Plant Proteins/genetics , Plants, Genetically Modified/cytology , Plants, Genetically Modified/genetics , Plants, Genetically Modified/metabolism , Seeds/cytology , Seeds/enzymology , Seeds/metabolism
2.
Mol Nutr Food Res ; 53 Suppl 2: S219, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19035553

ABSTRACT

Glucosinolates (GLSs) are found in Brassica vegetables. Examples of these sources include cabbage, Brussels sprouts, broccoli, cauliflower and various root vegetables (e.g. radish and turnip). A number of epidemiological studies have identified an inverse association between consumption of these vegetables and the risk of colon and rectal cancer. Animal studies have shown changes in enzyme activities and DNA damage resulting from consumption of Brassica vegetables or isothiocyanates, the breakdown products (BDP) of GLSs in the body. Mechanistic studies have begun to identify the ways in which the compounds may exert their protective action but the relevance of these studies to protective effects in the human alimentary tract is as yet unproven. In vitro studies with a number of specific isothiocyanates have suggested mechanisms that might be the basis of their chemoprotective effects. The concentration and composition of the GLSs in different plants, but also within a plant (e.g. in the seeds, roots or leaves), can vary greatly and also changes during plant development. Furthermore, the effects of various factors in the supply chain of Brassica vegetables including breeding, cultivation, storage and processing on intake and bioavailability of GLSs are extensively discussed in this paper.


Subject(s)
Brassica/chemistry , Diet/statistics & numerical data , Food Supply , Glucosinolates/administration & dosage , Health Status , Animals , Anticarcinogenic Agents/administration & dosage , Anticarcinogenic Agents/metabolism , Brassica/genetics , Brassica/metabolism , Breeding , Glucosinolates/analysis , Glucosinolates/metabolism , Humans
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