scholarly journals Transcriptome of the Australian Mollusc Dicathais orbita Provides Insights into the Biosynthesis of Indoles and Choline Esters

Marine Drugs ◽  
2016 ◽  
Vol 14 (7) ◽  
pp. 135 ◽  
Author(s):  
Abdul Baten ◽  
Ajit Ngangbam ◽  
Daniel Waters ◽  
Kirsten Benkendorff
Keyword(s):  
1949 ◽  
Vol 42 (6) ◽  
pp. 709-725 ◽  
Author(s):  
K. C. SWAN
Keyword(s):  

1970 ◽  
Vol 48 (10) ◽  
pp. 709-722 ◽  
Author(s):  
E. A. Hosein ◽  
A. Kato ◽  
E. Vine ◽  
A. M. Hill

Acetyl-l-carnitylcholine (l-ACCh) was identified in rat brain extracts on paper chromatograms developed in butanol–water for 138 h. l-ACCh was also identified in brain extracts fractionated on t.l.c. plates and on Sephadex G-10 columns. In every instance l-ACCh was separated from the acetylcholine (ACh) present and the ACh-like activity of l-ACCh was about 20% of the total activity in the extract. Both l-ACCh and ACh were found to be inseparable in a variety of chromatographic systems including electrophoresis. Treatment of these choline esters with cholinesterases showed that while true acetylcholinesterase hydrolyzed both l-ACCh and ACh, pseudocholinesterase destroyed only ACh. On a molar basis, the ACh-like activity of ACCh is one-half that of ACh on both the guinea pig ileum and frog rectus preparations. Like ACh, the ratio of the nicotinic to muscarinic potency of l-ACCh is unity. Mixtures of l-ACCh and ACh show summation of ACh-like activity on both the guinea pig ileum and frog rectus preparations.


1997 ◽  
Vol 31 (1) ◽  
pp. 23-26
Author(s):  
V. O. Topuzyan ◽  
G. Yu. Khachvakyan ◽  
L. V. Shakhbazyan ◽  
D. A. Gerasimyan
Keyword(s):  

1992 ◽  
Vol 284 (1) ◽  
pp. 153-160 ◽  
Author(s):  
Y B Kim ◽  
C H Jung ◽  
S J Choi ◽  
W J Seo ◽  
S H Cha ◽  
...  

The choline esters potentiated the choline-catalysed decarbamoylation of dimethylcarbamoyl-acetylcholinesterase in proportion to the length of acyl group, although esters containing an acyl chain longer than the hexanoyl group exhibited a corresponding decrease in the potentiation. In structural requirement analysis it was found that both the quaternary ammonium moiety and the ester bond were important for the effective acceleration of choline-catalysed decarbamoylation. In general, the respective thiocholine ester was found to be more effective than the corresponding choline ester. Whereas the binding affinity (Ka) of choline in the decarbamoylation was not significantly altered, the maximum decarbamoylation rate (kr(max.)) of choline was greatly enhanced in the presence of choline esters or thiocholine esters. Along with the above observation, the isotope solvent effect, the effect of ionic strength and the antagonism studies demonstrate that the choline esters or thiocholine esters may interact with one of peripheral anionic sites, and thereby make the choline-catalysed decarbamoylation more favourable.


1953 ◽  
Vol 7 ◽  
pp. 906-912 ◽  
Author(s):  
Klas-Bertil Augustinsson ◽  
Margareta Grahn ◽  
H. Fex ◽  
B. Högberg ◽  
T. Linderot ◽  
...  

1993 ◽  
Vol 115 (23) ◽  
pp. 10477-10482 ◽  
Author(s):  
Trevor Selwood ◽  
Shawn R. Feaster ◽  
Michael J. States ◽  
Alton N. Pryor ◽  
Daniel M. Quinn

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