Immunochemistry of the Group-Specific Polysaccharide of Nocardia brasiliensis

Abstract

of the group-specific polysaccharide of Nocardia brasiliensis. J. Bacteriol. 90:571-574. 1965.-The groupspecific polysaccharide of Nocardia brasiliensis was further purified, yielding an amorphous white material with the following characteristics: [a]D20 = + 48; nitrogen, 0.5%; phosphorus, 0.1%; and ash as sodium, 0.8%. The polymer is made of D-arabinose and D-galactose in a molar ratio of 3:1, and no other sugars were detected. Mild hydrolysis liberates mainly arabinose. The polysaccharide consumes 3.46,umoles of periodate per mg of polymer in 15 days at 4 C (this value remains constant after 4 more days). Oxidation results in destruction of two of the arabinose, with the formation of two glycerols after borohydride reduction and hydrolysis. The polysaccharide oxidized by periodate and reduced under mild acid hydrolysis at 20 C yields glycerol and a polymer formed by galactose and arabinose (in a ratio of 1:1) which is resistant to a second oxidation. Therefore, the polysaccharide is probably formed by a main chain of glactose linked 1,3 and arabinose linked 1,2 or 1,3 or both, and nonreducing side chains of arabofuranose residues. The intact polysaccharide cross-reacts with sera from patients with active tuberculosis, and this, as well as the homologous reaction, is abolished by oxidation with periodate.

Serological Study of Nocardia by Using Mycobacterial Precipitation Reference Systems

“…Nocardia and Mycobacterium have also been studied with serological methods such as agglutination, complement fixation, and sensitin tests as well as with immunodiffusion and immunoelectrophoresis. In these studies it has been shown that various species of Nocardia and Mycobacterium have antigens in common (1,3,7,10,11,13,14,26,27,42). Furthermore, with serological methods it has been possible to distinguish different species within the genus Nocardia (31, 32,41,46,51).…”