A new amperometric plant tissue biosensor based on the co-immobilisation of ground spinach leaves and ferrocene in a carbon paste matrix is described for the determination of glycolic acid. The spinach tissue acts as a source of glycolate oxidase and peroxidase. Ferrocene is employed as a mediator w
Multienzyme containing tissue-based and ferrocene-mediated bioelectrode for the determination of polyamines
β Scribed by Meng Shan Lin; Minoru Hare; Garry A. Rechnitz
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 483 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1040-0397
No coin nor oath required. For personal study only.
β¦ Synopsis
Oat seedling tissue and ferrocene/ferricinium were coimmobilized in a carbon paste matrix to construct a biosensor for polyamines. The oat tissue is rich in the enzymes polyamine oxidase and peroxidase while the mediator facilitates electron transfer between the electrode and hydrogen peroxide. The determination of the polyamines spermine and spermidine, in both batch and flow injection modes, was evaluated. The concentration of polyamine was monitored through hydrogen peroxide in the presence of oxygen as cosubstrate of polyamine oxidase. A reductive potential of 0.0 V was chosen for monitoring ferricinium which is generated by peroxidase. The detection limit (SJN = 3) for spermidine and spermine in the batch system was 0.19 and 1.15 pM, respectively. The relative standard deviation for twelve replicate analyses of 10 pM spermidine was 4.54%. The activity of the tissue moddied carbon paste electrode decreased to 45% of the original value after a storage for 8 days in buffer solution at 4Β°C.
π SIMILAR VOLUMES
## Abstract The biosynthetically doubleβlabeled lipopolysaccharide (LPS), containing ^3^Hβlabeled on the fatty acylβchains and ^14^Cβlabeled on the glucosamine of __Salmonella enterica serotype typhimurium__, was isolated from bacteria grown in proteose peptoneβbeef extract (PPBE) medium in the pre
A method for the analysis of S-adenosyl-L-methionine (SAM) and S-adenosyl-L-ethionine (SAE) and their major metabolites by high-performance liquid chromatography is described. The procedure allows the simultaneous analysis of the natural polyamines, putrescine, spermidine, and spermine, and some of