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Biomedical subjects

M Heidelberger

Publications and source records attributed to M Heidelberger.

At least 55 records · Page 3Linked to original sources

Immunochemistry of the capsular polysaccharide of an acinetobacter.

The capsular polysaccharide of a strain, BD4, of Acinetobacter calco-aceticus (A.c-a), composed of L-rhamnose and D-glucose, 4:1, precipitates all streptococcal group B antisera tested, as well as streptococcal group G antisera and antipneumococcal (Pn) type XXIII serum. Nonreducing end groups of L-rhamnose, known to be major determinants of the antigens giving rise to these antisera, are thus identified in A.c-a, which also precipitates anti-Pn VI sera. Both the rhamnose and glucose in the capsular polysaccharide (S) of Pn VI are linked 1,3-, as is the rhamnose in Pn S II, which also precipitates anti-Pn VI because of this linkage. A.c-a and S II precipitate the same fraction of anti-Pn VI, identifying a second portion of the rhamnose of A.c-a as 1,3-linked. This is confirmed by the stability of a portion of the rhamnose on oxidation of A.c-a with periodate, and 1,3-linked glucose or a periodate-stable branch point is also indicated in the same way. Two features of the fine structure of A.c-a have thus been established and a third indicated.

Bacteria↗

Predicted and unpredicted cross-reactions of an acetylphosphogalactan of Sporobolomyces yeast.

The teichoic acid of streptococcal Group N, with end groups of galactose phosphate, had been shown to cross-react with antipneumococcal sera of types VI, XIV, XVI, and XXVII. End groups of D-galactose-1-phosphate in the phosphogalactans of Sporobolomyces yeasts made it predictable that these galactans would precipitate the same antipneumococcal sera and also antisera to streptococcal Group N. The predictions were verified, and other unpredicted reactions were found. Precipitation of much of the antibody in an antipneumoccal type XVIII horse serum was shown to be due to O-acetyl-D-galactose residues in the phosphogalactan, in accord with earlier information that an O-acetyl sugar was a principal determinant of S XVIII. The new results identify this sugar as D-galactose. Since it is linked 1,3- in S XVIII, the O-acetyl group in the Sporobolomyces galactan is probably also on a 1,3-linked residue. Another major cross-reaction in anti-S. paratyphi A serum characterizes the galactose residues in the "O" polysaccharide of the bacillus as members of the D-series probably linked in tandem 1,6-, 1,6-; 1,6-, 1,3-; 1,3-, 1,6-; or 1,3-, 1,3-. Reactions of periodate-oxidized-reduced products confirm the conclusions stated above. Quantitative data are given.

Animals↗

The capsular polysaccharide of pneumococcus type IX.

The capsular polysaccharide of Type IX pneumococcus contains D-glucose, N-acetyl-D-glucosamine, and D-glucuronic acid. Complete hydrolysis is difficult. All of the N-acetylglucosamine is resistant to oxidation by periodate, but the other two sugars are degraded in part. Chemical and quantitative serological data are consistent with the linkage of two D-glucose residues 1 --> 4, as in maltose; others may be linked 1 --> 3. Part, at least, of the glucuronic acid and N-acetylglucosamine is linked to glucose.

In Vitro Techniques↗