Genotoxicity of pyrroloquinoline quinone (PQQ) disodium salt (BioPQQ™)

2013 ◽  
Vol 67 (2) ◽  
pp. 189-197 ◽  
Author(s):  
Masahiko Nakano ◽  
Hiroshi Suzuki ◽  
Tadashi Imamura ◽  
Annette Lau ◽  
Barry Lynch
2015 ◽  
Vol 61 (3) ◽  
pp. 241-246 ◽  
Author(s):  
Masahiko NAKANO ◽  
Ayako KAMIMURA ◽  
Fumiko WATANABE ◽  
Toshikazu KAMIYA ◽  
Daisuke WATANABE ◽  
...  

Author(s):  
Kazuto Ikemoto ◽  
Shigeki Mori ◽  
Kazuo Mukai

Pyrroloquinoline quinone (PQQ) is a water-soluble quinone compound first identified as a cofactor of alcohol- and glucose-dehydrogenases (ADH and GDH) in bacteria. For example, in the process of ADH reaction, alcohol is oxidized to the corresponding aldehyde, and inversely PQQ is reduced to pyrroloquinoline quinol (PQQH2). PQQ and PQQH2molecules play an important role as a cofactor in ADH and GDH reactions. However, crystal structure analysis has not been performed for PQQ and PQQH2. In the present study, the synthesis of PQQH2powder crystals was performed under air, by utilizing vitamin C as a reducing agent. By reacting a trihydrate of disodium salt of PQQ (PQQNa2·3H2O) with excess vitamin C in H2O at 293 and 343 K, yellowish brown and black powder crystals of PQQH2having different properties were obtained in high yield, respectively. The former was PQQH2trihydrate (PQQH2·3H2O) and the latter was PQQH2anhydrate (PQQH2). Furthermore, sodium-free red PQQ powder crystal (a monohydrate of PQQ, PQQ·H2O) was prepared by the reaction of PQQNa2·3H2O with HCl in H2O. Single crystals of PQQH2and PQQ were prepared from Me2SO/CH3CN mixed solvent, and we have succeeded in the crystal structure analyses of PQQH2and PQQ for the first time.


EFSA Journal ◽  
2017 ◽  
Vol 15 (11) ◽  
Author(s):  
◽  
Dominique Turck ◽  
Jean‐Louis Bresson ◽  
Barbara Burlingame ◽  
Tara Dean ◽  
...  

2014 ◽  
Vol 70 (1) ◽  
pp. 107-121 ◽  
Author(s):  
Masahiko Nakano ◽  
Hisaaki Takahashi ◽  
Seiko Koura ◽  
Catherine Chung ◽  
Shahrzad Tafazoli ◽  
...  

2015 ◽  
Vol 75 ◽  
pp. 146-150 ◽  
Author(s):  
Chunlai Liang ◽  
Xin Zhang ◽  
Wei Wang ◽  
Yan Song ◽  
Xudong Jia

2019 ◽  
Vol 17 (1) ◽  
pp. 544-556
Author(s):  
Yoke-Leng Sim ◽  
Beljit Kaur

AbstractPhosphate ester hydrolysis is essential in signal transduction, energy storage and production, information storage and DNA repair. In this investigation, hydrolysis of adenosine monophosphate disodium salt (AMPNa2) was carried out in acidic, neutral and alkaline conditions of pH ranging between 0.30-12.71 at 60°C. The reaction was monitored spectrophotometrically. The rate ranged between (1.20 ± 0.10) × 10-7 s-1 to (4.44 ± 0.05) × 10-6 s-1 at [NaOH] from 0.0008 M to 1.00M recorded a second-order base-catalyzed rate constant, kOH as 4.32 × 10-6 M-1 s-1. In acidic conditions, the rate ranged between (1.32 ± 0.06) × 10-7 s-1 to (1.67 ± 0.10) × 10-6 s-1 at [HCl] from 0.01 M to 1.00 M. Second-order acid-catalyzed rate constant, kH obtained was 1.62 × 10-6 M-1 s-1. Rate of reaction for neutral region, k0 was obtained from graphical method to be 10-7 s-1. Mechanisms were proposed to involve P-O bond cleavage in basic medium while competition between P-O bond and N-glycosidic cleavage was observed in acidic medium. In conclusion, this study has provided comprehensive information on the kinetic parameters and mechanism of cleavage of AMPNa2 which mimicked natural AMP cleavage and the action of enzymes that facilitate its cleavage.


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