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1.
Phytochemistry ; 115: 9-19, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25639596

ABSTRACT

Carnosic acid (salvin), which possesses antioxidative and antimicrobial properties, is increasingly exploited within the food, nutritional health and cosmetics industries. Since its first extraction from a Salvia species (∼70 years ago) and its identification (∼50 years ago), numerous articles and patents (∼400) have been published on specific food and medicinal applications of Rosmarinus and Salvia plant extracts abundant in carnosic acid. In contrast, relevant biochemical, physiological or molecular studies in planta have remained rare. In this overview, recent advances in understanding of carnosic acid distribution, biosynthesis, accumulation and role in planta, and its applications are summarised. We also discuss the deficiencies in our understanding of the relevant biochemical processes, and suggest the molecular targets of carnosic acid. Finally, future perspectives and studies related to its potential roles are highlighted.


Subject(s)
Abietanes/chemistry , Abietanes/pharmacology , Anti-Infective Agents/chemistry , Anti-Infective Agents/pharmacology , Antioxidants/chemistry , Antioxidants/pharmacology , Rosmarinus/chemistry , Salvia/chemistry , Abietanes/isolation & purification , Animals , Anti-Infective Agents/isolation & purification , Antioxidants/isolation & purification , Chromatography, High Pressure Liquid , Humans , Mice , Molecular Structure , Plant Leaves/chemistry , Rats , Rosmarinus/classification , Sheep
2.
Phytochem Anal ; 15(1): 9-15, 2004.
Article in English | MEDLINE | ID: mdl-14979520

ABSTRACT

A new, rapid HPLC-PAD-APCI/MS assay has been developed in order to measure accurately the amount of p-coumaric, E- and Z-ferulic acid and the dehydrodimers of ferulic acid in cereal grain. In the positive ionisation mode, MS patterns gave additional information for the identification of the dimers. The time required and the quantities of solvents employed in the developed analytical method are much lower than those involved in previously available assays of these compounds, thus making the method suitable for the screening of cereal genotypes. Application of the method to accessions of maize, wheat and sorghum showed that E-ferulic was the most abundant phenylpropanoid, whilst the major dimer was 8-O-4' dehydrodimer of ferulic acid followed by the 5-5' and then the 8-5' forms. Maize grains, especially of the Mexican landraces, contained the highest levels of these dimers.


Subject(s)
Chromatography, High Pressure Liquid/methods , Coumaric Acids/analysis , Edible Grain/chemistry , Gas Chromatography-Mass Spectrometry/methods , Oryza/chemistry , Propionates , Sorghum/chemistry , Triticum/chemistry , Zea mays/chemistry
3.
J Agric Food Chem ; 51(9): 2826-31, 2003 Apr 23.
Article in English | MEDLINE | ID: mdl-12696980

ABSTRACT

Four trichothecene-producing strains of Fusarium graminearum were grown on three maize grain fractions, whole grain, degermed grain, and the germ, to determine the effect of natural substrates on mycotoxin production. Monitoring the ergosterol content after 25 days of incubation indicated that fungal growth on all grain fractions was comparable. Trichothecene (TCT) production was highest on degermed grain, less on whole grain, and very low or nondetectable on the germ; similar results were found with four different strains. It was concluded that inhibitor(s) of TCT biosynthesis were present in maize germ. The presence of phenolic compounds was investigated in the different fractions. The hydroxamate 4-acetylbenzoxazolin-2-one (4-ABOA), a known inhibitor of mycotoxin production, was found in the degermed and whole grain fractions but not in the germ. Therefore, the TCT inhibition observed on the maize germ fraction used in our study is clearly not linked to 4-ABOA. Other soluble phenolic compounds were found at a much higher concentration in the germ than in the two other fractions. The inhibition property of the soluble ester-bound extracts was tested in liquid culture. A possible role for these compounds is discussed.


Subject(s)
Fusarium/metabolism , Phenols/metabolism , Trichothecenes/biosynthesis , Zea mays/microbiology , Zea mays/chemistry
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