Colorimetric Sensor for Triphosphates and Their Application as a Viable Staining Agent for Prokaryotes and Eukaryotes

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• 作者：Amrita Ghosh ; Anupama Shrivastav ; D. Amilan Jose ; Sanjiv K. Mishra ; C. K. Chandrakanth ; Sandhya Mishra ; Amitava Das
• 刊名：Analytical Chemistry
• 出版年：2008
• 出版时间：July 15, 2008
• 年：2008
• 卷：80
• 期：14
• 页码：5312 - 5319
• 全文大小：1036K
• 年卷期：v.80,no.14(July 15, 2008)
• ISSN：1520-6882

文摘

The chromogenic complex 1·Zn (where 1 is (E)-4-(4-dimethylamino-phenylazo)-N,N-bispyridin-2-ylmethyl-benzenesulfonamide) showed high affinity toward the phosphate ion in tetrabutylammonium phosphate in acetonitrile solution and could preferentially bind to adenosine triphosphate (ATP) in aqueous solution at physiological pH. This binding caused a visual change in color, whereas no such change was noticed with other related anions (adenosine monophosphate, adenosine diphosphate, pyrophosphate, and phosphate) of biological significance. Thus, 1·Zn could be used as a staining agent for different biological cells through binding to the ATP, generated in situ by the mitochondria (in eukaryotes). For prokaryotes (bacteria) the cell membrane takes care of the cells’ energy conversion, since they lack mitochondria. ATP is produced in their unique cell structure on the cell membrane, which is not found in any eukaryotes. These stained cells could be viewed with normal light microscopy. This reagent could even be used for distinguishing the Gram-positive and the Gram-negative bacteria (prokaryotes). This dye was found to be nonlipophilic in nature and nontoxic to living microbes (eukaryotes and prokaryotes). Further, stained cells were found to grow in their respective media, and this confirmed the maintenance of viability of the microbes even after staining, unlike with many other dyes available commercially.