Influence of NaCl and NaNO3 on Sinigrin Hydrolysis by Foodborne Bacteria

被引:18
作者
Herzallah, S. [2 ]
Lara Lledo, M. [3 ]
Holley, R. [1 ]
机构
[1] Univ Manitoba, Dept Food Sci, Winnipeg, MB R3T 2N2, Canada
[2] Mutah Univ, Dept Nutr & Food Sci, Al Karak, Jordan
[3] Inst Tecnol Embalaje Transporte & Logist ITENE, Valencia 46980, Spain
基金
加拿大自然科学与工程研究理事会;
关键词
ALLYL ISOTHIOCYANATE; ANTIMICROBIAL ACTIVITY; ROAST BEEF; FOOD; PLANTS; BRASSICACEAE; INHIBITION; MYROSINASE; PRODUCTS; GROWTH;
D O I
10.4315/0362-028X.JFP-11-284
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The glucosinolate sinigrin (SNG) is converted by endogenous plant myrosinase or by bacterial myrosinase-like activity to form the potent antimicrobial ally! isothiocyanate. In order to use SNG as a natural antimicrobial precursor in food, it became important to better understand the ability of bacteria to synthesize the enzyme(s) and understand factors influencing this synthesis at a constant SNG concentration. Eight spoilage, pathogenic, or starter culture bacteria were grown separately in medium containing individual or combined salts with SNG. SNG degradation by the bacteria and the formation of its major degradation product, allyl isothiocyanate, were followed for 12 days at 30 or 35 degrees C. The bacterial strains varied in their ability to metabolize SNG, and this was enhanced by NaCl and/or NaNO3. SNG hydrolysis took place after 4 days, and the greatest amount occurred by day 12. At 12 days, Escherichia coli O157:H7 showed the greatest capacity to hydrolyze SNG (45.3% degradation), followed by Staphylococcus carnosus (44.57%), while Pseudomonas fluorescens was not active against SNG. The ability of tested strains to metabolize SNG, in decreasing order, was as follows: Escherichia coli O157:H7 > Staphylococcus carnosus > Staphylococcus aureus > Pediococcus pentosaceus > Salmonella Typhimurium > Listeria monocyto genes > Enterococcus faecalis > Pseudomonas fluorescens.
引用
收藏
页码:2162 / 2168
页数:7
相关论文
共 36 条
[1]   Characterization of catalase and superoxide dismutase in Staphylococcus carnosus 833 strain [J].
Barrière, C ;
Leroy-Sétrin, S ;
Talon, R .
JOURNAL OF APPLIED MICROBIOLOGY, 2001, 91 (03) :514-519
[2]   Recent advances in cheese microbiology [J].
Beresford, TP ;
Fitzsimons, NA ;
Brennan, NL ;
Cogan, TM .
INTERNATIONAL DAIRY JOURNAL, 2001, 11 (4-7) :259-274
[3]   Glucosinolates, glycosidically bound volatiles and antimicrobial activity of Aurinia sinuata (Brassicaceae) [J].
Blazevic, Ivica ;
Radonic, Ani ;
Mastelic, Josip ;
Zekic, Marina ;
Skocibusic, Mirjana ;
Maravic, Ana .
FOOD CHEMISTRY, 2010, 121 (04) :1020-1028
[4]  
Bones AM, 1996, PHYSIOL PLANTARUM, V97, P194, DOI [10.1034/j.1399-3054.1996.970128.x, 10.1111/j.1399-3054.1996.tb00497.x]
[5]   THE EFFECTS OF GLUCOSINOLATES AND THEIR HYDROLYSIS PRODUCTS ON MICROBIAL-GROWTH [J].
BRABBAN, AD ;
EDWARDS, C .
JOURNAL OF APPLIED BACTERIOLOGY, 1995, 79 (02) :171-177
[6]   Glucosinolates in Brassica foods: Bioavailability in food and significance for human health [J].
Cartea M.E. ;
Velasco P. .
Phytochemistry Reviews, 2008, 7 (2) :213-229
[7]   Glycosidases in plant tissues of some Brassicaceae - Screening of different cruciferous plants for glycosidases production [J].
ElSayed, ST ;
Jwanny, EW ;
Rashad, MM ;
Mahmoud, AE ;
Abdallah, NM .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 1995, 55 (03) :219-230
[8]   The chemical diversity and distribution of glucosinolates and isothiocyanates among plants [J].
Fahey, JW ;
Zalcmann, AT ;
Talalay, P .
PHYTOCHEMISTRY, 2001, 56 (01) :5-51
[9]   GLUCOSINOLATES AND THEIR BREAKDOWN PRODUCTS IN FOOD AND FOOD PLANTS [J].
FENWICK, GR ;
HEANEY, RK ;
MULLIN, WJ .
CRC CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1983, 18 (02) :123-201
[10]   Effectiveness of antimicrobial coated oriented polypropylene/polyethylene films in sprout packaging [J].
Gamage, Gayani R. ;
Park, Hyun-Jin ;
Kim, Ki Myong .
FOOD RESEARCH INTERNATIONAL, 2009, 42 (07) :832-839