Portions of mouse brain, ktdneF and h~er were fixed wuh g[utaraldeh~de and the hp~ds were then extracted with chloroform methanol Comparison of the extracted hplds with those from stmdar porhons of the same unfixed hssues by thin la~,er chromatography sho~ed the absence of phosphatldyl ethanolamme i
Sites of reaction of glutaraldehyde and acetaldehyde with nucleosides
β Scribed by Kari Hemminki; Ritva Suni
- Publisher
- Springer-Verlag
- Year
- 1984
- Tongue
- English
- Weight
- 415 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0340-5761
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β¦ Synopsis
Glutaraldehyde, a dialdehyde, was reacted with ribonucleosides and deoxyribonucleosides and the products were purified by high-performance liquid chromatography (HPLC). Multiple reaction products were identified with cytosine- and purine-containing nucleosides. The products were labile, but spectroscopic evidence indicated that exocyclic amino groups were involved. Similar reactions were seen with acetaldehyde and butyraldehyde, monofunctional aldehydes. After reduction, one of the acetaldehyde-guanosine adducts was assigned the structure N2-ethylguanosine.
π SIMILAR VOLUMES
Glut~aIde~yde reacts with an excess of hydroxy~am~ne, hydrazine or methytamine through an intermediate that absorbs more strongly at 240 nm than do the end products. On the basis of the characteristic absorbance change during the reaction with hydroxylamine a spectrophotometric difference method was
The treatment of guanine nucleosides and nucleotides with excess acetaldehyde in pH 8.0 phosphate buffer containing a basic amino acid such as arginine and lysine resulted in the smooth and selective formation of the corresponding cyclic 1,N 2 -propano adducts even under mild conditions.
## Abstract The pulsed laser photolysis/laserβinduced fluorescence technique has been used to conduct additional measurements of the gasβphase CH~3~CHO + OH reaction. These measurements were conducted to verify the complex temperature dependence previously observed by the authors and to acquire mec