A MANNAN PRODUCED BY SACCHAROMYCES ROUXII

1956 ◽  
Vol 34 (12) ◽  
pp. 1796-1803 ◽  
Author(s):  
P. A. J. Gorin ◽  
A. S. Perlin

The main slime polysaccharide produced by Saccharomyccs rouxii during the fermentation of D-glucose to D-arabitol is a mannan. Acetolysis of the polymer has afforded di- and tri-saccharides in good yield, but no higher oligosaccharides were produced. The disaccharide is shown by methylation and lead tetraacetate oxidation to be 2-O-α-D-mannopyranosyl-D-mannose, establishing the presence of a 1,2-α-linkage in the polysaccharide. On acid hydrolysis the methylated mannan gives mainly 2,3,4,6-tetra-O-methyl-D-mannose, 3,4,6-tri-O-methyl-D-mannose, and 3,4-di-O-methyl-D-mannose; lesser components found are 2,4,6-tri-O-methyl-D-mannose and 3-O-methyl-D-mannose. The methylation and acetolysis data together suggest an average structural unit consisting of a main chain of D-mannopyranose units containing alternate 1,2- and 1,6-linkages, to which single D-mannopyranose units are attached by 1,2-linkages as side chains; alternatively, 1,2-disaccharide units are attached as side chains by 1,2-linkages to a 1,6-linked main chain.

1985 ◽  
Vol 38 (8) ◽  
pp. 1155 ◽  
Author(s):  
RP Kozyrod ◽  
JT Pinhey

The addition of lead tetraacetate to diphenylmercury in chloroform leads to the rapid formation of a solution of phenyllead triacetate, which has been used directly for the C-phenylation of ethyl 2-oxocyclopentanecarboxylate (1) and 2-nitropropane in good yield. This method of arylation has been examined for a range of diorganolead compounds and the β-keto ester (1), and the results indicate that the method should be widely applicable.


2020 ◽  
Vol 22 (40) ◽  
pp. 23385-23398
Author(s):  
Ivan V. Mikhailov ◽  
Ekaterina B. Zhulina ◽  
Oleg V. Borisov

Superimposed distributions of main chain ends in brush of comb polymers with different length and grafting density of side chains.


2007 ◽  
Vol 28 (10) ◽  
pp. 1115-1121 ◽  
Author(s):  
Wei Zhang ◽  
Masashi Shiotsuki ◽  
Toshio Masuda
Keyword(s):  

1955 ◽  
Vol 8 (4) ◽  
pp. 512 ◽  
Author(s):  
AJ Birch ◽  
J Cymerman-Craig ◽  
M Slaytor

The reduction by sodium and ethanol, with or without liquid ammonia as solvent, of various amidines followed by acid hydrolysis, leads in many cases to a good yield of the corresponding aldehyde. Further reduction in liquid ammonia of several 2-aryl-imidazolines or imidazolidines followed by acid hydrolysis leads to the 2,5-dihydro-benzaldehyde derivative. The reduction of some acid amides by sodium and proton sources in liquid ammonia has been examined. Under the right conditions this process is of preparative value for aldehydes.


2010 ◽  
Vol 66 (3) ◽  
pp. 268-275 ◽  
Author(s):  
Thomas C. Terwilliger

A method for the identification of α-helices in electron-density maps at low resolution followed by interpretation at moderate to high resolution is presented. Rapid identification is achieved at low resolution, where α-helices appear as tubes of density. The positioning and direction of the α-helices is obtained at moderate to high resolution, where the positions of side chains can be seen. The method was tested on a set of 42 experimental electron-density maps at resolutions ranging from 1.5 to 3.8 Å. An average of 63% of the α-helical residues in these proteins were built and an average of 76% of the residues built matched helical residues in the refined models of the proteins. The overall average r.m.s.d. between main-chain atoms in the modeled α-helices and the nearest atom with the same name in the refined models of the proteins was 1.3 Å.


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