A luminol chemiluminescence method for sensing histidine and lysine using enzyme reactions

2013 ◽  
Vol 443 (1) ◽  
pp. 22-26 ◽  
Author(s):  
Akimitsu Kugimiya ◽  
Rie Fukada ◽  
Daiki Funamoto
2009 ◽  
Vol 92 (3) ◽  
pp. 914-918 ◽  
Author(s):  
Aifang Li ◽  
Xiaoyu Liu ◽  
Juan Kong ◽  
Haoyu Hu ◽  
Linghui Sun ◽  
...  

Abstract A novel chemiluminescence method has been developed for the determination of the organophosphorous pesticide phosphamidon in environmental water samples, based on the reaction of phosphamidon with luminolH2O2 in an alkaline medium using sodium dodecyl benzene sulfonate as the enhancer. Under optimum conditions, the increased chemiluminescence intensity was proportional to the concentration of phosphamidon in the range of 0.011.0 g/mL and the detection limit was 0.0038 g/mL (3). The relative standard deviation was <2 for 0.5 g/mL phosphamidon (n = 11). The proposed method was applied to the determination of phosphamidon residue in an environmental water sample with satisfactory results. Further study was focused on the mechanism of phosphamidon, and a possible mechanism was proposed.


2007 ◽  
Vol 61 (7) ◽  
pp. 706-710 ◽  
Author(s):  
Xiaofeng Xie ◽  
Xili He ◽  
Zhenghua Song

A novel chemiluminescence method combined with the flow injection technique for the determination of carbon monoxide is presented in this paper. The chemiluminescence signal based on the reaction between myoglobin and luminol in an alkaline medium was remarkably enhanced by carbon monoxide. The enhanced chemiluminescence intensity was linear with carbon monoxide concentration in the range from 0.01 to 10.0 pmol·L−1, and the detection limit was 3 × 10−3 pmol·L−1 (3σ). The whole process, including sampling and washing, could be completed in 0.5 min with a relative standard deviation of less than 4.0%. The proposed method was applied successfully in the assay of carbon monoxide in human serum and artificial water samples without any pretreatment procedure.


2017 ◽  
Vol 952 ◽  
pp. 50-58 ◽  
Author(s):  
Hitoshi Kodamatani ◽  
Yoshimi Iwaya ◽  
Makoto Saga ◽  
Keiitsu Saito ◽  
Takahiro Fujioka ◽  
...  

2004 ◽  
Vol 9 (2) ◽  
pp. 139-144 ◽  
Author(s):  
J. Kulys

A model of biosensor containing three immobilized enzymes utilizing consecutive substrate conversion in the chain was developed. The modeling was performed at an internal diffusion limitation and a steadystate condition. The calculations showed that significant response of biosensors was produced if diffusion modules were larger than 1 for all enzyme reactions. Due to diffusion limitation the apparent stability of biosensor response increased many times in comparison to stability of the most labile enzyme of the chain.


2018 ◽  
Author(s):  
Justin Eilertsen ◽  
Santiago Schnell

<div>As a case study, we consider a coupled enzyme assay of sequential enzyme reactions obeying the Michaelis--Menten reaction mechanism. The sequential reaction consists of a single-substrate, single-enzyme non-observable reaction followed by another single-substrate, single-enzyme observable reaction (indicator reaction). In this assay, the product of the non-observable reaction becomes the substrate of the indicator reaction. A mathematical analysis of the reaction kinetics is performed, and it is found that after an initial fast transient, the sequential reaction is described by a pair of interacting Michaelis--Menten equations. Timescales that approximate the respective lengths of the indicator and non-observable reactions, as well as conditions for the validity of the Michaelis--Menten equations are derived. The theory can be extended to deal with more complex sequences of enzyme catalyzed reactions.</div>


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