Inactivation kinetics of gram-negative bacteria in the presence of residual free chlorine

2021 ◽  
Vol 210 ◽  
pp. 222-230
Author(s):  
Pankaj Kumar Roy ◽  
Minakshi Ghosh
2006 ◽  
Vol 132 (7) ◽  
pp. 818-823 ◽  
Author(s):  
Irene Xagoraraki ◽  
Gregory W. Harrington ◽  
Kimberly Zulliger ◽  
Benjamim Zeier ◽  
William Krick ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (9) ◽  
pp. e0184671 ◽  
Author(s):  
David A. Westfall ◽  
Ganesh Krishnamoorthy ◽  
David Wolloscheck ◽  
Rupa Sarkar ◽  
Helen I. Zgurskaya ◽  
...  

2013 ◽  
Vol 295-298 ◽  
pp. 599-603
Author(s):  
Feng Liu ◽  
Zhong Lin Chen ◽  
Sheng Chang

The object of this paper is to measure the characteristics of the inactivation kinetics of B. subtilis spores-surrogates for B. anthracis spores following the treatment with free chlorine. The results indicated that the inactivation kinetics of B. subtilis spores with free chlorine was characterized by a lag phase followed by a pseudo-first-order rate of inactivation. The magnitude of the lag phase increased and the rate of subsequent inactivation decreased with the decreasing temperature, for the experimental temperature range of 1-30 °C. The same tendency of inactivation kinetics curves was observed for the increasing solution pH, for the experimental pH range of 6-8. The CT concept was proved to be valid for the inactivation kinetics of B. subtilis spores with free chlorine under the conditions investigated. The validity of B. subtilis spores served as conservative surrogates for B. anthracis spore has been finally discussed.


AQUASAINS ◽  
2019 ◽  
Vol 7 (1) ◽  
pp. 647
Author(s):  
Esti Harpeni ◽  
Supono Supono ◽  
Dwi Risca Septiani

Isolate D2.2 is a bacterial isolate with 97% homology level with Bacillus sp. This isolate is a biocontrol bacterium capable of inhibiting the growth of Gram positive bacteria and Gram negative bacteria. The use of biocontrol bacteria is one solution of disease problem in cultivation organism. Prior to being applied to the field, D2.2 isolates need to go through a series of tests, one of which is growth kinetics testing under various environmental conditions, such as different degrees of pH and salinity. This is because environmental factors can affect the rapid growth of bacteria. The purpose of this study was to study the bacterial growth kinetics of D2.2 at different pH and salinity. The growth kinetics was observed by measuring optical density (OD) through a method of turbidimetry using a spectrophotometer at a wavelength of 625 nm to the stage of death. The results showed that the fastest growth rate was found at 20 ppt salinity with 0.179 h-1 and generation time of 5,588 hours. While in all pH treatments, generation time and growth rates achieved all treatments have the same pattern.


1959 ◽  
Vol 42 (5) ◽  
pp. 917-922 ◽  
Author(s):  
C. L. Baugh ◽  
J. B. Clark

The photodynamic lethal response of Gram negative bacteria was found to be a one event phenomenon as previously reported. However, the kinetics of the lethal response in Gram-positive microorganisms was found to be more complex. The survivor response of the latter was dividable into at least two distinct parts, each of which could be influenced by various environmental and genetic factors. Some correlation was found between sensitivity or resistance to x-ray and ultraviolet radiations and sensitivity or resistance to photodynamic action.


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