Colorimetric detection of catalase and catalase-positive bacteria (E. coli) using silver nanoprisms

2016 ◽  
Vol 8 (36) ◽  
pp. 6625-6630 ◽  
Author(s):  
Lili Zhao ◽  
Julia Wiebe ◽  
Rabia Zahoor ◽  
Sladjana Slavkovic ◽  
Brian Malile ◽  
...  

The sensitivity of the formation of plasmonic silver nanoprisms to hydrogen peroxide is explored for the colorimetric detection of catalase activity in bacteria.

1999 ◽  
Vol 65 (1) ◽  
pp. 73-79 ◽  
Author(s):  
Nobutoshi Ichise ◽  
Naoki Morita ◽  
Tamotsu Hoshino ◽  
Kosei Kawasaki ◽  
Isao Yumoto ◽  
...  

ABSTRACT A possible mechanism of resistance to hydrogen peroxide (H2O2) in Vibrio rumoiensis, isolated from the H2O2-rich drain pool of a fish processing plant, was examined. When V. rumoiensiscells were inoculated into medium containing either 5 mM or no H2O2, they grew in similar manners. A spontaneous mutant strain, S-4, derived from V. rumoiensisand lacking catalase activity did not grow at all in the presence of 5 mM H2O2. These results suggest that catalase is inevitably involved in the resistance and survival of V. rumoiensis in the presence of H2O2. Catalase activity was constitutively present in V. rumoiensis cells grown in the absence of H2O2, and its occurrence was dependent on the age of the cells, a characteristic which is observed for the HP II-type catalase of Escherichia coli. The presence of the HP II-type catalase in V. rumoiensis cells was evidenced by partial sequencing of the gene encoding the HP II-type catalase from this organism. A notable difference between V. rumoiensisand E. coli is that catalase is accumulated at very high levels (∼2% of the total soluble proteins) in V. rumoiensis, in contrast to the case for E. coli. WhenV. rumoiensis cells which had been exposed to 5 mM H2O2 were centrifuged, most intracellular proteins, including catalase, were recovered in the medium. On the other hand, when V. rumoiensis cells were grown on plates containing various concentrations of H2O2, individual cells had a colony-forming ability inferior to those ofE. coli, Bacillus subtilis, and Vibrio parahaemolyticus. Thus, it is suggested that when V. rumoiensis cells are exposed to high concentrations of H2O2, most cells will immediately be broken by H2O2. In addition, the cells which have had little or no damage will start to grow in a medium where almost all H2O2 has been decomposed by the catalase released from broken cells.


2003 ◽  
Vol 71 (1) ◽  
pp. 550-556 ◽  
Author(s):  
Hsing-Ju Tseng ◽  
Alastair G. McEwan ◽  
Michael A. Apicella ◽  
Michael P. Jennings

ABSTRACT It has been reported that Neisseria gonorrhoeae possesses a very high level of catalase activity, but the regulation of catalase expression has not been investigated extensively. In Escherichia coli and Salmonella enterica serovar Typhimurium, it has been demonstrated that OxyR is a positive regulator of hydrogen peroxide-inducible genes, including the gene encoding catalase. The oxyR gene from N. gonorrhoeae was cloned and used to complement an E. coli oxyR mutant, confirming its identity and function. The gene was inactivated by inserting a kanamycin resistance cassette and used to make a knockout allele on the chromosome of N. gonorrhoeae strain 1291. In contrast to E. coli, the N. gonorrhoeae oxyR::kan mutant expressed ninefold-more catalase activity and was more resistant to hydrogen peroxide killing than the wild type. These data are consistent with OxyR in N. gonorrhoeae acting as a repressor of catalase expression.


1998 ◽  
Vol 180 (8) ◽  
pp. 2087-2092 ◽  
Author(s):  
Karen L. Visick ◽  
Edward G. Ruby

ABSTRACT The catalase gene, katA, of the sepiolid squid symbiontVibrio fischeri has been cloned and sequenced. The predicted amino acid sequence of KatA has a high degree of similarity to the recently defined group III catalases, including those found in Haemophilus influenzae, Bacteroides fragilis, and Proteus mirabilis. Upstream of the predicted start codon of katA is a sequence that closely matches the consensus sequence for promoters regulated inEscherichia coli by the alternative sigma factor encoded byrpoS. Further, the level of expression of the clonedkatA gene in an E. coli rpoS mutant is much lower than in wild-type E. coli. Catalase activity is induced three- to fourfold both as growing V. fischericells approach stationary phase and upon the addition of a small amount of hydrogen peroxide during logarithmic growth. The catalase activity was localized in the periplasm of wild-type V. fischeri cells, where its role could be to detoxify hydrogen peroxide coming from the external environment. No significant catalase activity could be detected in a katA null mutant strain, demonstrating that KatA is the predominately expressed catalase inV. fischeri and indicating that V. fischeri carries only a single catalase gene. The catalase mutant was defective in its ability to competitively colonize the light organs of juvenile squids in coinoculation experiments with the parent strain, suggesting that the catalase enzyme plays an important role in the symbiosis between V. fischeri and its squid host.


2021 ◽  
Vol 13 (14) ◽  
pp. 1706-1714
Author(s):  
Nianlu Li ◽  
Mingquan Zhu ◽  
Zhenyu Feng ◽  
Wenhui Lu ◽  
Jing Chen ◽  
...  

In this work, cystine–glucose Maillard conjugates were composited with Cu1.8S microspheres (Cu1.8S–cgmc) to achieve higher sensitivity for the colorimetric analysis.


1982 ◽  
Vol 152 (1) ◽  
pp. 81-88
Author(s):  
E H Berglin ◽  
M B Edlund ◽  
G K Nyberg ◽  
J Carlsson

Under anaerobic conditions an exponentially growing culture of Escherichia coli K-12 was exposed to hydrogen peroxide in the presence of various compounds. Hydrogen peroxide (0.1 mM) together with 0.1 mM L-cysteine or L-cystine killed the organisms more rapidly than 10 mM hydrogen peroxide alone. The exposure of E. coli to hydrogen peroxide in the presence of L-cysteine inhibited some of the catalase. This inhibition, however, could not fully explain the 100-fold increase in hydrogen peroxide sensitivity of the organism in the presence of L-cysteine. Of other compounds tested only some thiols potentiated the bactericidal effect of hydrogen peroxide. These thiols were effective, however, only at concentrations significantly higher than 0.1 mM. The effect of L-cysteine and L-cystine could be annihilated by the metal ion chelating agent 2,2'-bipyridyl. DNA breakage in E. coli K-12 was demonstrated under conditions where the organisms were killed by hydrogen peroxide.


Author(s):  
Bing Han ◽  
Xiaoyu Han ◽  
Mengmeng Ren ◽  
Yilin You ◽  
Jicheng Zhan ◽  
...  

Diseases caused by harmful microorganisms pose a serious threat to human health. Safe and environment-friendly disinfectants are, therefore, essential in preventing and controlling such pathogens. This study aimed to investigate the antimicrobial activity and mechanism of a novel hydrogen peroxide and silver (H 2 O 2 -Ag + ) complex (HSC) in combatting Staphylococcus aureus ATCC 29213, Escherichia coli O157:H7 NCTC 12900 and Salmonella typhimurium SL 1344. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values against S. aureus were found to be 0.014 % H 2 O 2 -3.125 mg/L Ag + , while 0.028 % H 2 O 2 -6.25 mg/L Ag + for both E. coli and S. typhimurium . Results of the growth curve assay and time-kill trial suggest that the HSC could inhibit the growth of the tested bacteria, as 99.9 % of viable cells were killed following treatment at the 1 MIC for 3 h. Compared with Oxytech D10 disinfectant (0.25 % H 2 O 2 -5 mg/L Ag + ), the HSC exhibited better antibacterial efficacy at a lower concentration (0.045 % H 2 O 2 -10 mg/L Ag + ). The mechanism of antibacterial action of HSC was found including the disruption of the bacterial cell membrane, followed by entry into the bacteria cell to reduce intracellular adenosine triphosphate (ATP) concentration, and inhibit the activity of antioxidases, superoxide dismutase (SOD) and catalase (CAT). The enhanced bactericidal effect of hydrogen peroxide combined with silver indicates a potential for its application in environmental disinfection, particularly in the food industry.


1992 ◽  
Vol 27 (1) ◽  
pp. 57-68 ◽  
Author(s):  
D.W. Sundstrom ◽  
B.A. Weir ◽  
T. A. Barber ◽  
H. E. Klei

Abstract This project investigated the destruction of organic compounds and microorganisms in water by ultraviolet catalyzed oxidation using hydrogen peroxide as the oxidizing agent. The combination of UV light and hydrogen peroxide was effective in decomposing all of the organic compounds studied. The rates of destruction increased with increasing peroxide concentration and UV light intensity, and were highly dependent on chemical structure. The destruction of mixtures of organic compounds showed strong interactions between reacting components. The inactivation of E. coli and B. subtilis spores by UV light and/or hydrogen peroxide was studied in flat plate reactors. By using thin liquid films, the combination of UV light and peroxide greatly increased the rates of inactivation of both microorganisms. The results were correlated by a mixed second order kinetic model.


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