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Grant: Research Tools and Instruments - Category 1 (<$150,000)

University of Manitoba

$109,543.00

HPLC system with photodiode array (PDA) and evaporative light scattering (ELS)detectors

EF 2014-15

Résumé
This application requests the purchase of a high performance liquid chromatograph (HPLC) to be used in characterizing the degradation of mustard glucosinolates by bacteria. Industrial deodorization of mustard powder permits this ingredient to be used as a protein supplement in processed meat products because the endogenous plant enzyme, myrosinase, is destroyed during thermal treatment, giving the powder neutral flavour and odour characters. Glucosinolates in the powder and amended products remain unchanged in terms of colour and flavour. We have discovered that many foodborne pathogens such as toxigenic E. coli, Salmonella, Campylobacter, and Listeria monocytogenes use a myrosinase-like enzyme(s), and intracellularly transform the mustard glucosinolates into isothiocyanates which are lethal to the producing organism. Thus, deodorized mustard can be used as a natural antimicrobial in food. Initial studies indicated that when glucose was readily available, myrosinase synthesis and glucosinolate utilization were repressed in target bacteria, so further study is planned to optimize enzyme synthesis by altering environmental exposures and studying genetic control of enzyme synthesis in growing and resting cells to broaden application of this unique antimicrobial approach. HPLC analysis of glucosinolate dissimilation represents the cornerstone of this work and is essential to identify factors influencing myrosinase synthesis and glucosinolate degradation by bacteria. At present the 22 year-old HPLC used for these analyses is prone to frequent failures and requires expensive replacement parts when these are available (operational software is only partially functional and the data storage format is obsolete). The high demand placed on use of this equipment makes access to alternate equipment, often remote from the Department, an impractical solution. Studies by 9 HQP working on NSERC Discovery-funded research conducted by the 3 applicants (Holley, 4 students; Arntfield, 2 students, protein-phenolic compound interactions on texture/flavour functionality; Scanlon, 3 students, gas phase effects on food texture) will be able to complete their work with this equipment.
Programme
Research Tools and Instruments - Category 1 (<$150,000)
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
472945-2015
Name nom
Holley, Richard
Department département
Food Science
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2015
Award amount
109543
Program id
EQPEQ
Program name en
Research Tools and Instruments - Category 1 (<$150,000)
Program name fr
Outils et instruments de recherche - catégorie 1 (<150 000$)
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
501
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Processed food products and beverages
Area of application fr
Aliments transformés et boissons
Research subject code
6102
Research subject group en
Food science and technology
Research subject group fr
Science et technologie de l'alimentation
Research subject en
Food microbiology
Research subject fr
Microbiologie alimentaire
Partie
1
Nb partie
1
Application title
HPLC system with photodiode array (PDA) and evaporative light scattering (ELS)detectors
Keyword
NSERC
Application summary
This application requests the purchase of a high performance liquid chromatograph (HPLC) to be used in characterizing the degradation of mustard glucosinolates by bacteria. Industrial deodorization of mustard powder permits this ingredient to be used as a protein supplement in processed meat products because the endogenous plant enzyme, myrosinase, is destroyed during thermal treatment, giving the powder neutral flavour and odour characters. Glucosinolates in the powder and amended products remain unchanged in terms of colour and flavour. We have discovered that many foodborne pathogens such as toxigenic E. coli, Salmonella, Campylobacter, and Listeria monocytogenes use a myrosinase-like enzyme(s), and intracellularly transform the mustard glucosinolates into isothiocyanates which are lethal to the producing organism. Thus, deodorized mustard can be used as a natural antimicrobial in food. Initial studies indicated that when glucose was readily available, myrosinase synthesis and glucosinolate utilization were repressed in target bacteria, so further study is planned to optimize enzyme synthesis by altering environmental exposures and studying genetic control of enzyme synthesis in growing and resting cells to broaden application of this unique antimicrobial approach. HPLC analysis of glucosinolate dissimilation represents the cornerstone of this work and is essential to identify factors influencing myrosinase synthesis and glucosinolate degradation by bacteria. At present the 22 year-old HPLC used for these analyses is prone to frequent failures and requires expensive replacement parts when these are available (operational software is only partially functional and the data storage format is obsolete). The high demand placed on use of this equipment makes access to alternate equipment, often remote from the Department, an impractical solution. Studies by 9 HQP working on NSERC Discovery-funded research conducted by the 3 applicants (Holley, 4 students; Arntfield, 2 students, protein-phenolic compound interactions on texture/flavour functionality; Scanlon, 3 students, gas phase effects on food texture) will be able to complete their work with this equipment.