Electrochemical study on 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one-added zinc coating in phosphate buffer saline medium with Escherichia coli

2015 ◽  
Vol 19 (8) ◽  
pp. 2213-2222 ◽  
Author(s):  
Xiaofan Zhai ◽  
Xiumin Ma ◽  
Maria Myamina ◽  
Jizhou Duan ◽  
Baorong Hou
2010 ◽  
Vol 36 (1) ◽  
pp. 51-56
Author(s):  
Kazuhiro Asami ◽  
Akira Inaba ◽  
Kazuhisa Ohtaguchi

2000 ◽  
Vol 63 (6) ◽  
pp. 703-708 ◽  
Author(s):  
MARCY A. WISNIEWSKY ◽  
BONITA A. GLATZ ◽  
MARK L. GLEASON ◽  
CHERYLL A. REITMEIER

The objectives of this study were to determine if washing of whole apples with solutions of three different sanitizers (peroxyacetic acid, chlorine dioxide, or a chlorine-phosphate buffer solution) could reduce a contaminating nonpathogenic Escherichia coli O157:H7 population by 5 logs and at what sanitizer concentration and wash time such a reduction could be achieved. Sanitizers were tested at 1, 2, 4, 8, and 16 times the manufacturer's recommended concentration at wash times of 5, 10, and 15 min. Whole, sound Braeburn apples were inoculated with approximately 1 × 108 or 7 × 106 CFU per apple, stored for 24 h, then washed with sterile water (control) or with sanitizers for the prescribed time. Recovered bacteria were enumerated on trypticase soy agar. Washing with water alone reduced the recoverable population by almost 2 logs from the starting population; this can be attributed to physical removal of organisms from the apple surface. No sanitizer, when used at the recommended concentration, reduced the recovered E. coli population by 5 logs under the test conditions. The most effective sanitizer, peroxyacetic acid, achieved a 5-log reduction when used at 2.1 to 14 times its recommended concentration, depending on the length of the wash time. The chlorine-phosphate buffer solution reduced the population by 5 logs when used at 3 to 15 times its recommended concentration, depending on wash time. At no concentration or wash time tested did chlorine dioxide achieve the 5-log reduction.


1950 ◽  
Vol 3 (1) ◽  
pp. 28 ◽  
Author(s):  
W Joklik

A method of purifying the nitrate reductase obtained by crushingEscherichia coli cells in a ground glass mill is described, involving elution atpH 9.5 and precipitation into slightly acidified acetone, followed by treatmentwith phosphate buffer ( pH 8.0) and dialysis. Methods of estimating theactivity of the enzyme without recourse to coupling with other enzymes areoutlined, viz.: (a) the oxidation time method; (b) the use of photochemicallyreduced methylene blue as hydrogen donor.


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