The myrosinase-glucosinolate system in the interaction between Leptosphaeria maculans and Brassica napus.

summary Leptosphaeria maculans causes blackleg disease, and resistance to this fungal pathogen is an important trait in the breeding of oilseed rape. A better comprehension of the role of the myrosinase-glucosinolate system in this context is of great value. The present study is the first to address effects on multiple components of this complex system, including concentrations of individual glucosinolates, product formation, myrosinase isoform distribution and activity, and levels of myrosinase binding proteins during the infection process. One resistant B. napus cultivar (Maluka) and one susceptible cultivar (Westar) were compared in the investigation. Our results show that the two cultivars had the same histological distribution, isoform expression, and activity of the myrosinase enzymes. The glucosinolate levels were also similar, with the exception of glucobrassicin and neoglucobrassicin, which were significantly lower in the resistant cultivar at 11 days post-infection. Growth of the fungus on the plant tissues did not alter glucosinolate levels, suggesting that L. maculans does not degrade these compounds. When the plants were starved of sulphur, and thereby depleted of glucosinolates, no increased susceptibility was observed. Hence, we suggest that the myrosinase-glucosinolate system does not determine the outcome of the interaction between B. napus and L. maculans.

[1]  B. Thomma,et al.  Study of the role of antimicrobial glucosinolate-derived isothiocyanates in resistance of Arabidopsis to microbial pathogens. , 2001, Plant physiology.

[2]  J. Xue,et al.  Identification and characterization of soluble and insoluble myrosinase isoenzymes in different organs of Sinapis alba. , 2001, Physiologia plantarum.

[3]  C. Dixelius,et al.  B-genome derived resistance to Leptosphaeria maculans in near isogenic Brassica napus lines is independent of glucosinolate profile. , 2000 .

[4]  B. Howlett,et al.  Characterisation of a cyanide hydratase gene in the phytopathogenic fungus Leptosphaeria maculans , 2000, Molecular and General Genetics MGG.

[5]  B. Halkier,et al.  Functional expression and characterization of the myrosinase MYR1 from Brassica napus in Saccharomyces cerevisiae. , 1999, Protein expression and purification.

[6]  D. Silué,et al.  Glucosinolates in cauliflower as biochemical markers for resistance against downy mildew , 1999 .

[7]  C. Dixelius,et al.  Resistance to Leptosphaeria maculans is conserved in a specific region of the Brassica B genome , 1999, Theoretical and Applied Genetics.

[8]  E. Andreasson,et al.  Co-localization of myrosinase- and myrosinase-binding proteins in grains of myrosin cells in cotyledon of Brassica napus seedlings , 1998 .

[9]  A. Brandt,et al.  Two jasmonate-inducible myrosinase-binding proteins from Brassica napus L. seedlings with homology to jacalin , 1998, Planta.

[10]  S. Eriksson,et al.  The myrosinase-binding protein from Brassica napus seeds possesses lectin activity and has a highly similar vegetatively expressed wound-inducible counterpart. , 1997, European journal of biochemistry.

[11]  S. Eriksson,et al.  Regulation of the wound-induced myrosinase-associated protein transcript in Brassica napus plants. , 1997, European Journal of Biochemistry.

[12]  L. Lazzeri,et al.  In Vitro Fungitoxic Activity of Some Glucosinolates and Their Enzyme-Derived Products toward Plant Pathogenic Fungi , 1997 .

[13]  R. Mithen,et al.  Glucosinolates and disease resistance in oilseed rape (Brassica napus ssp. oleifera) , 1997 .

[14]  Atle M. Bones,et al.  THE MYROSINASE-GLUCOSINOLATE SYSTEM, ITS ORGANISATION AND BIOCHEMISTRY , 1996 .

[15]  L. Rask,et al.  A Wound- and Methyl Jasmonate-Inducible Transcript Coding for a Myrosinase-Associated Protein with Similarities to an Early Nodulin , 1996, Plant physiology.

[16]  S. Michaelsen,et al.  Separation of desulphoglucosinolates by micellar electrokinetic capillary chromatography based on a bile salt , 1995 .

[17]  R. Wallsgrove,et al.  Salicylic acid-induced accumulation of glucosinolates in oilseed rape (Brassica napus L.) leaves , 1994 .

[18]  J. Lewis,et al.  Oviposition and tarsal chemoreceptors of the cabbage root fly are stimulated by glucosinolates and host plant extracts , 1992 .

[19]  L. Josefsson,et al.  Immunological characterization of rapeseed myrosinase. , 1990, European journal of biochemistry.

[20]  F. S. Chew Biological effects of glucosinolates , 1989 .

[21]  R. Mithen,et al.  Resistance of leaves of Brassica species to Leptosphaeria maculans , 1987 .

[22]  R. Mithen,et al.  In vitro activity of glucosinolates and their products against Leptosphaeria maculans , 1986 .

[23]  D. Janzen,et al.  Herbivores: Their Interaction With Secondary Plant Metabolites , 1982 .

[24]  N. Mitchell,et al.  THE INVOLVEMENT OF FLAVOUR VOLATILES IN THE RESISTANCE TO DOWNY MILDEW OF WILD AND CULTIVATED FORMS OF BRASSICA OLERACEA , 1976 .

[25]  M. H. Beale,et al.  Detection and cellular localization of elemental sulphur in disease-resistant genotypes of Theobroma cacao , 1996, Nature.

[26]  N. Wratten,et al.  Blackleg disease on oilseed Brassica in Australia: a review , 1995 .

[27]  J. Pickett,et al.  Selective induction of glucosinolates in oilseed rape leaves by methyl jasmonate , 1995 .

[28]  M. Lenman,et al.  Sequence of a cDNA clone encoding the enzyme myrosinase and expression of myrosinase in different tissues of Brassica napus , 1992 .

[29]  P. Williams,et al.  Relationship between pathogenicity and phylogeny based on restriction fragment length polymorphism in Leptosphaeria maculans. , 1991 .

[30]  S. Louda,et al.  Chapter 4 – Glucosinolates: Chemistry and Ecology , 1991 .

[31]  M. Lenman,et al.  Distribution of myrosinase in rapeseed tissues. , 1991, Plant physiology.

[32]  E. J. Evans,et al.  Changes in glucosinolate concentrations during the vegetative growth of single and double-low cultivars of winter oilseed rape , 1989 .