Full text
PDF































Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- AKAMATSU Y., NOJIMA S. SEPARATION AND ANALYSES OF THE INDIVIDUAL PHOSPHOLIPIDS OF MYCOBACTERIA. J Biochem. 1965 Mar;57:430–439. doi: 10.1093/oxfordjournals.jbchem.a128097. [DOI] [PubMed] [Google Scholar]
- ARTMAN M., BEKIERKUNST A., GOLDENBERG I. TISSUE METABOLISM IN INFECTION: BIOCHEMICAL CHANGES IN MICE TREATED WITH CORD FACTOR. Arch Biochem Biophys. 1964 Apr;105:80–85. doi: 10.1016/0003-9861(64)90237-1. [DOI] [PubMed] [Google Scholar]
- ASSELINEAU J., BUC H., JOLLES P., LEDERER E. Sur la structure chimique d'une fraction peptido-glycolipidique (cire D) isolée de Mycobacterium tuberculosis var. hominis. Bull Soc Chim Biol (Paris) 1958;40(12):1953–1964. [PubMed] [Google Scholar]
- ASSELINEAU J., LEDERER E. Recherches récentes sur la chimie des lipides du bacille tuberculeux. Experientia. 1951 Aug 15;7(8):281–290. doi: 10.1007/BF02150541. [DOI] [PubMed] [Google Scholar]
- ASSELINEAU J. Lipides du bacille tuberculeux; constitution chimique et activité biologique. Bibl Tuberc. 1952;6:1–55. [PubMed] [Google Scholar]
- AZUMA I., KIMURA H., YAMAMURA Y. ISOLATION OF ARABINOSE MYCOLATE FROM WAX D FRACTION OF HUMAN TYPE TUBERCLE BACILLUS AOYAMA B STRAIN. J Biochem. 1965 Apr;57:571–572. doi: 10.1093/oxfordjournals.jbchem.a128116. [DOI] [PubMed] [Google Scholar]
- AZUMA I., YAMAMURA Y. Studies on the firmly bound lipids of human tubercle bacillus. I. Isolation of arabinose mycolate. J Biochem. 1962 Sep;52:200–206. doi: 10.1093/oxfordjournals.jbchem.a127597. [DOI] [PubMed] [Google Scholar]
- AZUMA I., YAMAMURA Y. Studies on the firmly bound lipids of human tubercle bacillus. J Biochem. 1963 Apr;53:275–281. [PubMed] [Google Scholar]
- Adam A., Petit J. F., Wietzerbin-Falszpan J., Sinay P., Thomas D. W., Lederer E. L'acide N-glycolyl-muramique, constituant des parois de Mycobacterium smegmatis: Identification par spectrometrie de masse. FEBS Lett. 1969 Jul;4(2):87–92. doi: 10.1016/0014-5793(69)80203-6. [DOI] [PubMed] [Google Scholar]
- Adam A., Senn M., Vilkas E., Lederer E. Spectrométrie de masse de glycolipides. 2. Diesters de tréhalose naturels et synthétiques. Eur J Biochem. 1967 Nov;2(4):460–468. doi: 10.1111/j.1432-1033.1967.tb00160.x. [DOI] [PubMed] [Google Scholar]
- Akamatsu Y., Law J. H. Enzymatic alkylenation of phospholipid fatty acid chains by extracts of Mycobacterium phlei. J Biol Chem. 1970 Feb 25;245(4):701–708. [PubMed] [Google Scholar]
- Akamatsu Y., Law J. H. Enzymatic synthesis of 10-methylene stearic acid and tuberculostearic acid. Biochem Biophys Res Commun. 1968 Oct 10;33(1):172–176. doi: 10.1016/0006-291x(68)90274-x. [DOI] [PubMed] [Google Scholar]
- Akamatsu Y., Ono Y., Nojima S. Phospholipid patterns in subcellular fractions of Mycobacterium phlei. J Biochem. 1966 Feb;59(2):176–182. doi: 10.1093/oxfordjournals.jbchem.a128279. [DOI] [PubMed] [Google Scholar]
- Akamatsu Y., Ono Y., Nojima S. Studies on the metabolism of phospholipids in Mycobacterium phlei. I. Difference in turnover rates of individual phospholipids. J Biochem. 1967 Jan;61(1):96–102. doi: 10.1093/oxfordjournals.jbchem.a128525. [DOI] [PubMed] [Google Scholar]
- Anacker R. L., Barclay W. R., Brehmer W., Goode G., List R. H., Ribi E., Tarmina D. F. Effectiveness of cell walls of Mycobacterium bovis strain BCG administered by various routes and in different adjuvants in protecting mice against airborne infection with Mycobacterium tuberculosis strain H37Rv. Am Rev Respir Dis. 1969 Feb;99(2):242–248. doi: 10.1164/arrd.1969.99.2.242. [DOI] [PubMed] [Google Scholar]
- Anacker R. L., Bickel W. D., Brehmer W., Niwa M., Ribi E., Tarmina D. F. Immunization of mice by combinations of inactive fractions of Mycobacterium bovis strain BCG. Proc Soc Exp Biol Med. 1969 Mar;130(3):723–730. doi: 10.3181/00379727-130-33642. [DOI] [PubMed] [Google Scholar]
- Antoine A. D., Tepper B. S. Environmental control of glycogen and lipid content of Mycobacterium phlei. J Gen Microbiol. 1969 Feb;55(2):217–226. doi: 10.1099/00221287-55-2-217. [DOI] [PubMed] [Google Scholar]
- Antoine A. D., Tepper B. S. Environmental control of glycogen and lipid content of Mycobacterium tuberculosis. J Bacteriol. 1969 Oct;100(1):538–539. doi: 10.1128/jb.100.1.538-539.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Asselineau C. P., Lacave C. S., Montrozier H. L., Promé J. C. Relations structurales entre les acides mycoliques insaturés et les acides inférieurs insaturés synthétisés par Mycobacterium phlei. Implications métaboliques. Eur J Biochem. 1970 Jul;14(3):406–410. doi: 10.1111/j.1432-1033.1970.tb00304.x. [DOI] [PubMed] [Google Scholar]
- Asselineau C., Montrozier H., Prome J. C. Structure des acides alpha-mycoliques isolés de la souche Canetti de Mycobacterium tuberculosis. Bull Soc Chim Fr. 1969 Feb;2:592–596. [PubMed] [Google Scholar]
- Asselineau C., Montrozier H., Promé J. C. Présence d'acides polyinsaturés dans une bactérie: isolement, à partir des lipides de Mycobacterium phlei, d'acide hexatriacontapentaène-4,8,12, 16, 20-oïque et d'acides analogues. Eur J Biochem. 1969 Oct;10(3):580–584. doi: 10.1111/j.1432-1033.1969.tb00728.x. [DOI] [PubMed] [Google Scholar]
- Azuma I., Kimura H., Yamamura Y. Chemical and immunological properties of polysaccharides of wax D extracted from Mycobacterium tuberculosis strain Aoyama B. J Bacteriol. 1968 Aug;96(2):567–568. doi: 10.1128/jb.96.2.567-568.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Azuma I., Thomas D. W., Adam A., Ghuysen J. M., Bonaly R., Petit J. F., Lederer E. Occurrence of N-glycolylmuramic acid in bacterial cell walls. A preliminary survey. Biochim Biophys Acta. 1970 Jun;208(3):444–451. doi: 10.1016/0304-4165(70)90217-5. [DOI] [PubMed] [Google Scholar]
- Azuma I., Yamamura Y., Fukushi K. Fractionation of mycobacterial cell wall. Isolation of arabinose mycolate and arabinogalactan from cell wall fraction of Mycobacterium tuberculosis strain Aoyama B. J Bacteriol. 1968 Nov;96(5):1885–1887. doi: 10.1128/jb.96.5.1885-1887.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Azuma I., Yamamura Y., Misaki A. Isolation and characterization of arabinose mycolate from firmly bound lipids of mycobacteria. J Bacteriol. 1969 Apr;98(1):331–333. doi: 10.1128/jb.98.1.331-333.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BEKIERKUNST A., ARTMAN M. Tissue metabolism in infection. DPNase activity, DPN levels, and DPN-linked dehydrogenases in tissues from normal and tuberculous mice. Am Rev Respir Dis. 1962 Dec;86:832–838. doi: 10.1164/arrd.1962.86.6.832. [DOI] [PubMed] [Google Scholar]
- BLOCH H. Studies on the virulence of tubercle bacilli; isolation and biological properties of a constituent of virulent organisms. J Exp Med. 1950 Feb;91(2):197-218, pl. doi: 10.1084/jem.91.2.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bekierkunst A., Levij I. S., Yarkoni E., Vilkas E., Adam A., Lederer E. Granuloma formation induced in mice by chemically defined mycobacterial fractions. J Bacteriol. 1969 Oct;100(1):95–102. doi: 10.1128/jb.100.1.95-102.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bekierkunst A., Levij I. S., Yarkoni E., Vilkas E., Lederer E. Cellular reaction in the footpad and draining lymph nodes of mice induced by mycobacterial fractions and BCG bacilli. Infect Immun. 1971 Sep;4(3):245–255. doi: 10.1128/iai.4.3.245-255.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bekierkunst A., Yarkoni E., Flechner I., Morecki S., Vilkas E., Lederer E. Immune response to sheep red blood cells in mice pretreated with mycobacterial fractions. Infect Immun. 1971 Sep;4(3):256–263. doi: 10.1128/iai.4.3.256-263.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bennet P., Asselineau J. Essais d'inhibition spécifique de la croissance du bacille tuberculeux. I. Inhibition de la synthèse des acides phtiénoïques et mycocérosiques. Ann Inst Pasteur (Paris) 1968 Apr;114(4):436–451. [PubMed] [Google Scholar]
- Bennet P., Asselineau J. Influence de l'âge sur la teneur en acides gras à chaîne ramifiée du bacille tuberculeux. Ann Inst Pasteur (Paris) 1970 Mar;118(3):324–329. [PubMed] [Google Scholar]
- Bonhomme F., Boucheron C., Migliore D., Jollès P. Arthritogenicity and protective effect against adjuvant arthritis of wax Ds fractions (glycolipids without a nitrogen-containing moiety) of Mycobacterium tuberculosis var. hominis and bovis. Experientia. 1968 Jul 15;24(7):716–717. doi: 10.1007/BF02138335. [DOI] [PubMed] [Google Scholar]
- Bonhomme F., Boucheron C., Migliore D., Jollès P. Arthritogenicity of unaltered and acetylated cell walls of mycobacteria. Int Arch Allergy Appl Immunol. 1969;36(3):317–320. doi: 10.1159/000230752. [DOI] [PubMed] [Google Scholar]
- Bonhomme F., Boucheron C., Migliore D., Jollès P. Nouvelles recherches concernant l'effet inhibiteur exercé par des fractions acétylées de cires D provenant de Mycobacterium tuberculosis var. hominis sur les propriétés arthrogènes des cires D (fractions petdoglycolipidiques) non modifiées. C R Acad Sci Hebd Seances Acad Sci D. 1967 Dec 18;265(25):2115–2117. [PubMed] [Google Scholar]
- Bordet C., Michel G. Structure et biogenèse des lipides a haut poids moléculaire de Nocardia asteroides. Bull Soc Chim Biol (Paris) 1969 Jul 25;51(3):527–548. [PubMed] [Google Scholar]
- Brehmer W., Anacker R. L., Ribi E. Immunogenicity of cell walls from various mycobacteria against airborne tuberculosis in mice. J Bacteriol. 1968 Jun;95(6):2000–2004. doi: 10.1128/jb.95.6.2000-2004.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brennan P. J., Rooney S. A., Winder F. G. The lipids of Mycobacterium tuberculosis BCG: fractionation, composition, turnover and the effects of isoniazid. Ir J Med Sci. 1970 Aug;3(8):371–390. doi: 10.1007/BF02956904. [DOI] [PubMed] [Google Scholar]
- Brennan P., Ballou C. E. Biosynthesis of mannophosphoinositides by Mycobacterium phlei. Enzymatic acylation of the dimannophosphoinositides. J Biol Chem. 1968 Jun 10;243(11):2975–2984. [PubMed] [Google Scholar]
- Brennan P., Ballou C. E. Biosynthesis of mannophosphoinositides by Mycobacterium phlei. The family of dimannophosphoinositides. J Biol Chem. 1967 Jul 10;242(13):3046–3056. [PubMed] [Google Scholar]
- CASON J., MILLER W. T. Complexity of the mixture of fatty acids from tubercle bacillus; C16 and C17 acids from virulent strains. J Biol Chem. 1963 Mar;238:883–887. [PubMed] [Google Scholar]
- CATEL W., SCHMIDT W. Klinische und experimentelle Untersuchungen über das Wesen der lokalen Tuberkulinempfindlichkeit. Dtsch Med Wochenschr. 1950 Sep 1;75(35):1140–1145. doi: 10.1055/s-0028-1117632. [DOI] [PubMed] [Google Scholar]
- CHAPUT M., MICHEL G., LEDERER E. [Structure of mycoside Cm, peptidoglycolipid of Mycobacterium marianum]. Biochim Biophys Acta. 1962 Sep 24;63:310–326. doi: 10.1016/0006-3002(62)90685-6. [DOI] [PubMed] [Google Scholar]
- CROWLE A. J. Immunizing constituents of the tubercle bacillus. Bacteriol Rev. 1958 Sep;22(3):183–203. doi: 10.1128/br.22.3.183-203.1958. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CUMMINS C. S., HARRIS H. The chemical composition of the cell wall in some gram-positive bacteria and its possible value as a taxonomic character. J Gen Microbiol. 1956 Jul;14(3):583–600. doi: 10.1099/00221287-14-3-583. [DOI] [PubMed] [Google Scholar]
- Campbell I. M., Naworal J. Composition of the saturated and monounsaturated fatty acids of Mycobacterium phlei. J Lipid Res. 1969 Sep;10(5):593–598. [PubMed] [Google Scholar]
- Campbell I. M., Naworal J. Mass spectral discrimination between monoenoic and cyclopropanoid, and between normal, iso, and anteiso fatty acid methyl esters. J Lipid Res. 1969 Sep;10(5):589–592. [PubMed] [Google Scholar]
- Cunto G., Kanetsuna F., Imaeda T. Chemical analysis of the mucopeptide of Mycobacterium smegmatis. Biochim Biophys Acta. 1969 Nov 18;192(2):358–360. doi: 10.1016/0304-4165(69)90378-x. [DOI] [PubMed] [Google Scholar]
- DEWIJS H., JOLLES P. CELL WALLS OF THREE STRAINS OF MYCOBACTERIA (MYCOBACTERIUM PHLEI, MYCOBACTERIUM FORTUITUM AND MYCOBACTERIUM KANSASII). PREPARATION, ANALYSIS AND DIGESTION BY LYSOZYMES OF DIFFERENT ORIGINS. Biochim Biophys Acta. 1964 Nov 1;83:326–332. [PubMed] [Google Scholar]
- Das B. C., Gero S. D., Lederer E. N-methylation of N-acyl oligopeptides. Biochem Biophys Res Commun. 1967 Oct 26;29(2):211–215. doi: 10.1016/0006-291x(67)90589-x. [DOI] [PubMed] [Google Scholar]
- David H. L., Goldman D. S., Takayama K. Inhibition of the Synthesis of Wax D Peptidoglycolipid of Mycobacterium tuberculosis by d-Cycloserine. Infect Immun. 1970 Jan;1(1):74–77. doi: 10.1128/iai.1.1.74-77.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- David H. L., Takayama K., Goldman D. S. Susceptibility of mycobacterial D-alanyl-D-alanine synthetase to D-cycloserine. Am Rev Respir Dis. 1969 Oct;100(4):579–581. doi: 10.1164/arrd.1969.100.4.579. [DOI] [PubMed] [Google Scholar]
- ETEMADI A. H., GASCHE J., SIFFERLEN J. IDENTIFICATION D'HOMOLOGUES SUP'ERIEURS DES ACIDES CORYNOMYCOLIQUE ET CORYNOMYCOL'ENIQUE DANS LES LIPIDES DE CORYNEBACTERIUM 506. Bull Soc Chim Biol (Paris) 1965;47:631–638. [PubMed] [Google Scholar]
- ETEMADI A. H., LEDERER E. BIOSYNTHESE DE L'ACIDE ALPHA-SMEGMA-MYCOLIQUE. Biochim Biophys Acta. 1965 Feb 1;98:159–167. [PubMed] [Google Scholar]
- Etemadi A. H. Corrélations structurales et biogénétiques des acides mycoliques en rapport avec la phylogenèse de quelques genres d'Actinomycétales. Bull Soc Chim Biol (Paris) 1967;49(6):695–706. [PubMed] [Google Scholar]
- Etemadi A. H., Lederer E. Sur la structure des acides alpha-mycoliques de la souche humaine test de Mycobacterium tuberculosis. Bull Soc Chim Fr. 1965 Sep;9:2640–2645. [PubMed] [Google Scholar]
- FREGNAN G. B., SMITH D. W., RANDALL H. M. A mutant of a scotochromogenic Mycobacterium detected by colony morphology and lipid studies. J Bacteriol. 1962 Apr;83:828–836. doi: 10.1128/jb.83.4.828-836.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferguson J. A., Ballou C. E. Biosynthesis of a mycobacterial lipopolysaccharide. Properties of the polysaccharide methyltransferase. J Biol Chem. 1970 Aug 25;245(16):4213–4223. [PubMed] [Google Scholar]
- GANGADHARAM P. R., COHN M. L., MIDDLEBROOK G. INFECTIVITY, PATHOGENICITY AND SULPHOLIPID FRACTION OF SOME INDIAN AND BRITISH STRAINS OF TUBERCLE BACILLI. Tubercle. 1963 Dec;44:452–455. doi: 10.1016/s0041-3879(63)80087-2. [DOI] [PubMed] [Google Scholar]
- GASTAMBIDE ODIER M., DELAUMENY J. M., LEDERER E. BIOSYNTH'ESE DE L'ACIDE C32-MYCOC'EROSIQUE; INCORPORATION D'ACIDE PROPIONIQUE. Biochim Biophys Acta. 1963 Dec 27;70:670–678. doi: 10.1016/0006-3002(63)90811-4. [DOI] [PubMed] [Google Scholar]
- GASTAMBIDE-ODIER M., DELAUMENY J. M., LEDERER E. MISE EN 'EVIDENCE DE CYCLES PROPANIQUES DANS DIVERS ACIDES MYCOLIQUES DE SOUCHES HUMAINES ET BOVINES DE MYCOBACTERIUM TUBERCULOSIS. C R Hebd Seances Acad Sci. 1964 Nov 9;259:3404–3407. [PubMed] [Google Scholar]
- Gastambide-Odier M., Lederer E., Sarda P. Structure des aglycones des mycosides A et B. Tetrahedron Lett. 1965 Sep;(35):3135–3143. doi: 10.1016/s0040-4039(01)89234-0. [DOI] [PubMed] [Google Scholar]
- Gastambide-Odier M., Sarda P. Contribution à l'étude de la structure et de la biosynthèse de glycolipides spécifiques isolés de mycobactéries: les mycosides a et b. Pneumonologie. 1970;142(2):241–255. doi: 10.1007/BF02095222. [DOI] [PubMed] [Google Scholar]
- Gastambide-Odier M., Sarda P., Lederer E. Biosynthèse des aglycones des mycosides A et B. Bull Soc Chim Biol (Paris) 1967 Jul 27;49(7):849–864. [PubMed] [Google Scholar]
- Ghuysen J. M. Use of bacteriolytic enzymes in determination of wall structure and their role in cell metabolism. Bacteriol Rev. 1968 Dec;32(4 Pt 2):425–464. [PMC free article] [PubMed] [Google Scholar]
- Goldman D. S. Subcellular localization of individual mannose-containing phospholipids in Mycobacterium tuberculosis. Am Rev Respir Dis. 1970 Oct;102(4):543–555. doi: 10.1164/arrd.1970.102.4.543. [DOI] [PubMed] [Google Scholar]
- Goren M. B., Brokl O., Das B. C., Lederer E. Sulfolipid I of Mycobacterium tuberculosis, strain H37RV. Nature of the acyl substituents. Biochemistry. 1971 Jan 5;10(1):72–81. doi: 10.1021/bi00777a012. [DOI] [PubMed] [Google Scholar]
- Goren M. B. Improved surface culturing of Mycobacterium tuberculosis. J Bacteriol. 1967 Oct;94(4):1258–1259. doi: 10.1128/jb.94.4.1258-1259.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goren M. B. Mycobacterial sulfolipids: spontaneous desulfation. Lipids. 1971 Jan;6(1):40–46. doi: 10.1007/BF02536373. [DOI] [PubMed] [Google Scholar]
- Goren M. B. Sulfolipid I of Mycobacterium tuberculosis, strain H37Rv. I. Purification and properties. Biochim Biophys Acta. 1970 Jun 9;210(1):116–126. doi: 10.1016/0005-2760(70)90067-6. [DOI] [PubMed] [Google Scholar]
- Goren M. B. Sulfolipid I of Mycobacterium tuberculosis, strain H37Rv. II. Structural studies. Biochim Biophys Acta. 1970 Jun 9;210(1):127–138. doi: 10.1016/0005-2760(70)90068-8. [DOI] [PubMed] [Google Scholar]
- Gorhe D., Asso J., Paraf A. Effet du traitement préalable par les adjuvants de l'immunité sur la muliplication du virus de la fièvre aphteuse chez la souris adulte. Ann Inst Pasteur (Paris) 1968 Sep;115(3):446–464. [PubMed] [Google Scholar]
- Hill D. L., Ballou C. E. Biosynthesis of mannophospholipids by Mycobacterium phlei. J Biol Chem. 1966 Feb 25;241(4):895–902. [PubMed] [Google Scholar]
- Hung J. G., Walker R. W. Unsaturated fatty acids of Mycobacteria. Lipids. 1970 Aug;5(8):720–722. doi: 10.1007/BF02531442. [DOI] [PubMed] [Google Scholar]
- IKAWA M., SNELL E. E., LEDERER E. Occurrence of D-phenylalanine, D-allothreonine and other D-amino-acids in peptido-lipids of bacterial origin. Nature. 1960 Nov 12;188:558–560. doi: 10.1038/188558a0. [DOI] [PubMed] [Google Scholar]
- Ilton M., Jevans A. W., McCarthy E. D., Vance D., White H. B., 3rd, Bloch K. Fatty acid synthetase activity in Mycobacterium phlei: regulation by polysaccharides. Proc Natl Acad Sci U S A. 1971 Jan;68(1):87–91. doi: 10.1073/pnas.68.1.87. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Inoue K., Nojima S. Immunochemical studies of phospholipids. 3. Production of antibody to cardiolipin. Biochim Biophys Acta. 1967 Oct 2;144(2):409–414. [PubMed] [Google Scholar]
- Ishibashi T., Fijiwara Y., Tanaka A., Sugiyama K. Antigenicity of wax D. IV. Its relationship to other hemagglutination reactions. Int Arch Allergy Appl Immunol. 1969;36(5):506–514. [PubMed] [Google Scholar]
- JOLLES P., NGUYEN-TRUNG-LUONG-CROS H., LEDERER E. [On the chemical structure of the peptide moiety of wax D from a human strain of Mycobacterium tuberculosis]. Biochim Biophys Acta. 1960 Oct 7;43:559–561. doi: 10.1016/0006-3002(60)90486-8. [DOI] [PubMed] [Google Scholar]
- JOLLES P., SAMOUR MIGLIORE D., DEWIJS H., LEDERER E. CORRELATION OF ADJUVANT ACTIVITY AND CHEMICAL STRUCTURE OF MYCOBACTERIAL WAX D FRACTIONS: THE IMPORTANCE OF AMINO SUGARS. Biochim Biophys Acta. 1964 Nov 1;83:361–363. doi: 10.1016/0926-6526(64)90018-7. [DOI] [PubMed] [Google Scholar]
- JOLLES P., SAMOUR D., LEDERER E. ISOLEMENT DE FRACTIONS PEPTIDO-GLYCOLIPIDIQUES 'A PARTIR DES CIRES D DE MYCOBACT'ERIES BOVINES, ATYPIQUES, AVIAIRES ET SAPROPHYTES. Biochim Biophys Acta. 1963 Oct 29;78:342–350. doi: 10.1016/0006-3002(63)91644-5. [DOI] [PubMed] [Google Scholar]
- JOLLES P., SMOUR D., LEDERER E. Analytical studies on wax D, a macromolecular peptidoglycoplied fraction from humn strains of Mycobacterium tuberculosos. Arch Biochem Biophys. 1962 Sep;Suppl 1:283–289. [PubMed] [Google Scholar]
- Jollès P., Migliore D., Bonhomme F. Wax D, peptido-glycolipid of Mycobacterium tuberculosis: further purification and study of an adjuvant arthritis inhibiting subfraction. Immunology. 1968 Feb;14(2):159–163. [PMC free article] [PubMed] [Google Scholar]
- KARLSSON J. L. Auxotrophic mutants of mycobacteria dependent on fatty acids derived from the parent strain. J Bacteriol. 1956 Dec;72(6):813–815. doi: 10.1128/jb.72.6.813-815.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KOTANI S., HASHIMOTO S., MATSUBARA T., KATO K., HARADA K., KOGAMI J. LYSIS OF ISOLATED BCG CELL WALLS WITH ENZYMES. 2. DEMONSTRATION OF 'BOUND WAX D' AS A COMPONENT OF BCG CELL WALLS. Biken J. 1963 Oct;6:181–196. [PubMed] [Google Scholar]
- Kanai K., Wiegeshaus E., Smith D. W. Demonstration of mycobacterial lipids in bacilli separated from infected tissue. Pneumonologie. 1970;142(2):224–231. doi: 10.1007/BF02095220. [DOI] [PubMed] [Google Scholar]
- Kanai K., Wiegeshaus E., Smith D. W. Demonstration of mycolic acid and phthiocerol dimycocerosate in "in vivo grown tubercle bacilli". Jpn J Med Sci Biol. 1970 Oct;23(5):327–333. [PubMed] [Google Scholar]
- Kanemasa Y., Goldman D. S. Direct incorporation of octanoate into long-chain fatty acids by soluble enzymes of Mycobacterium tuberculosis. Biochim Biophys Acta. 1965 Jun 1;98(3):476–485. doi: 10.1016/0005-2760(65)90144-x. [DOI] [PubMed] [Google Scholar]
- Kanetsuna F., Blas G. S. Chemical analysis of a mycolic acid-arabinogalactan-mucopeptide complex of mycobacterial cell wall. Biochim Biophys Acta. 1970 Jun;208(3):434–443. doi: 10.1016/0304-4165(70)90216-3. [DOI] [PubMed] [Google Scholar]
- Kanetsuna F. Chemical analyses of mycobacterial cell walls. Biochim Biophys Acta. 1968 Apr 16;158(1):130–143. doi: 10.1016/0304-4165(68)90080-9. [DOI] [PubMed] [Google Scholar]
- Kanetsuna F., Imaeda T., Cunto G. On the linkage between mycolic acid and arabinogalactan in phenol-treated myobacterial cell walls. Biochim Biophys Acta. 1969 Mar 11;173(2):341–344. doi: 10.1016/0005-2736(69)90117-5. [DOI] [PubMed] [Google Scholar]
- Kataoka T., Nojima S. Immunochemical studies of phospholipids. VI. Haptenic activity of phosphatidylinositol and the role of lecithin as an auxiliary lipid. J Immunol. 1970 Aug;105(2):502–511. [PubMed] [Google Scholar]
- Kato K., Strominger J. L., Kotani S. Structure of the cell wall of Corynebacterium diphtheriae. I. Mechanism of hydrolysis by the L-3 enzyme and the structure of the peptide. Biochemistry. 1968 Aug;7(8):2762–2773. doi: 10.1021/bi00848a010. [DOI] [PubMed] [Google Scholar]
- Kato K., Strominger J. L. Structure of the cell wall of Staphylococcus aureaus. IX. Mechanism of hydrolysis by the L11 enzyme. Biochemistry. 1968 Aug;7(8):2745–2761. [PubMed] [Google Scholar]
- Kato M., Asselineau J. Chemical structure and biochemical activity of cord factor analogs. 6,6'-Dimycoloyl sucrose and methyl 6-mycoloyl- -D-glucoside. Eur J Biochem. 1971 Oct 14;22(3):364–370. doi: 10.1111/j.1432-1033.1971.tb01553.x. [DOI] [PubMed] [Google Scholar]
- Kato M., Fukushi K. Studies of a biochemical lesion in experimental tuberculosis in mice. X. Mitochondrial swelling induced by cord factor in vivo and accompanying biochemical change. Am Rev Respir Dis. 1969 Jul;100(1):42–46. doi: 10.1164/arrd.1969.100.1.42. [DOI] [PubMed] [Google Scholar]
- Kato M. Molecular configuration and toxicity of cord factor. Jpn J Med Sci Biol. 1970 Aug;23(4):267–271. [PubMed] [Google Scholar]
- Kato M. Site II-specific inhibition of mitochondria oxidative phosphorylation by trehalose-6,6'-dimycolate (cord factor) of Mycobacterium tuberculosis. Arch Biochem Biophys. 1970 Oct;140(2):379–390. doi: 10.1016/0003-9861(70)90079-2. [DOI] [PubMed] [Google Scholar]
- Kato M. Site of action of the cord factor of Corynebacterium diphtheriae in mitochondria. J Bacteriol. 1971 Sep;107(3):746–752. doi: 10.1128/jb.107.3.746-752.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kato M. Studies of a biochemical lesion in experimental tuberculosis in mice. 3. Site of lesion in electron transport chain. Am Rev Respir Dis. 1966 Sep;94(3):388–394. doi: 10.1164/arrd.1966.94.3.388. [DOI] [PubMed] [Google Scholar]
- Kato M. Studies of a biochemical lesion in experimental tuberculosis in mice. 8. Effect of derivatives and chemical analogues of cord factor on structure and function of mouse liver mitochondria. Am Rev Respir Dis. 1968 Oct;98(4):668–676. doi: 10.1164/arrd.1968.98.4.668. [DOI] [PubMed] [Google Scholar]
- Kato M. Studies of a biochemical lesion in experimental tuberculosis in mice. VI. Effect of toxic bacterial constituents of tubercle bacilli on oxidative phosphorylation in host cell. Am Rev Respir Dis. 1967 Nov;96(5):998–1008. doi: 10.1164/arrd.1967.96.5.998. [DOI] [PubMed] [Google Scholar]
- Kato M. Studies of a biochemical lesion in experimental tuberculosis in mice. XI. Mitochondrial swelling induced by cord factor in vitro. Am Rev Respir Dis. 1969 Jul;100(1):47–53. doi: 10.1164/arrd.1969.100.1.47. [DOI] [PubMed] [Google Scholar]
- Keller J., Ballou C. E. The 6-O-methylglucose-containing lipopolysaccharide of Mycobacterium phlei. Identification of the lipid components. J Biol Chem. 1968 Jun 10;243(11):2905–2910. [PubMed] [Google Scholar]
- Khuller G. K., Subrahmanyam D. On the mannophosphoinositides of Mycobacterium 607. Experientia. 1968 Aug 15;24(8):851–852. doi: 10.1007/BF02144914. [DOI] [PubMed] [Google Scholar]
- LEDERER E. Glycolipids of acid-fast bacteria. Adv Carbohydr Chem. 1961;16:207–238. doi: 10.1016/s0096-5332(08)60263-5. [DOI] [PubMed] [Google Scholar]
- LENNARZ W. J., SCHEUERBRANDT G., BLOCH K. The biosynthesis of oleic and 10-methylstearic acids in Mycobacterium phlei. J Biol Chem. 1962 Mar;237:664–671. [PubMed] [Google Scholar]
- LONG E. R., ANDERSON R. J., RITTENBERG D., KARNOVSKY M. L., HENDERSON H. J. The carbon metabolism of the tubercle bacillus; studies with isotopic carbon. Am Rev Tuberc. 1955 May;71(5):609–615. doi: 10.1164/artpd.1955.71.5.609. [DOI] [PubMed] [Google Scholar]
- LYNEN F. Biosynthesis of saturated fatty acids. Fed Proc. 1961 Dec;20:941–951. [PubMed] [Google Scholar]
- Laneelle G., Asselineau J. Structure d'un glycoside de peptidolipide isolé d'une mycobactérie. Eur J Biochem. 1968 Sep 24;5(4):487–491. doi: 10.1111/j.1432-1033.1968.tb00396.x. [DOI] [PubMed] [Google Scholar]
- Lanéelle M. A., Lanéelle G. Structure d'acides mycoliques et d'un intermediaire dans la biosynthèse d'acides mycoliques dicarboxyliques. Eur J Biochem. 1970 Feb;12(2):296–300. doi: 10.1111/j.1432-1033.1970.tb00850.x. [DOI] [PubMed] [Google Scholar]
- Lederer E. The mycobacterial cell wall. Pure Appl Chem. 1971;25(1):135–165. doi: 10.1351/pac197125010135. [DOI] [PubMed] [Google Scholar]
- Lee Y. C., Ballou C. E. Complete structures of the glycophospholipids of mycobacteria. Biochemistry. 1965 Jul;4(7):1395–1404. doi: 10.1021/bi00883a026. [DOI] [PubMed] [Google Scholar]
- Lee Y. C. Isolation and characterization of lipopolysaccharides containing 6-O-methyl-D-glucose from Mycobacterium species. J Biol Chem. 1966 Apr 25;241(8):1899–1908. [PubMed] [Google Scholar]
- Liu T. Y., Gotschlich E. C. Muramic acid phosphate as a component of the mucopeptide of Gram-positive bacteria. J Biol Chem. 1967 Feb 10;242(3):471–476. [PubMed] [Google Scholar]
- Lornitzo F. A., Goldman D. S. Intracellular localization of a 6-O-methyl-D-glucose containing soluble polysaccharide from Mycobacterium tuberculosis. Biochim Biophys Acta. 1968 Jun 24;158(3):329–335. doi: 10.1016/0304-4165(68)90286-9. [DOI] [PubMed] [Google Scholar]
- MACLENNAN A. P., RANDALL H. M., SMITH D. W. The occurence of methyl ethers of rhamose and fucose in specific glycolipids of certain mycobacteria. Biochem J. 1961 Aug;80:309–318. doi: 10.1042/bj0800309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MACLENNAN A. P. The monosaccharide units in specific glycolipids of Mycobacterium avium. Biochem J. 1962 Mar;82:394–400. doi: 10.1042/bj0820394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Majerus P. W., Vagelos P. R. Fatty acid biosynthesis and the role of the acyl carrier protein. Adv Lipid Res. 1967;5:1–33. [PubMed] [Google Scholar]
- Markovits J., Vilkas E. Etude des cires D d'une souche humaine virulente de Mycobacterium tuberculosis. Biochim Biophys Acta. 1969 Oct 7;192(1):49–54. [PubMed] [Google Scholar]
- Markovits J., Vilkas E., Lederer E. Sur la structure chimique des cires D, peptidoglycolipides macromoléculaires des souches humaines de Mycobacterium tuberculosis. Eur J Biochem. 1971 Jan;18(2):287–291. doi: 10.1111/j.1432-1033.1971.tb01242.x. [DOI] [PubMed] [Google Scholar]
- Matsumura S., Brindley D. N., Bloch K. Acyl carrier protein from Mycobacterium phlei. Biochem Biophys Res Commun. 1970 Feb 6;38(3):369–377. doi: 10.1016/0006-291x(70)90723-0. [DOI] [PubMed] [Google Scholar]
- Matsumura S. Conformation of acyl carrier protein from Mycobacterium phlei. Biochem Biophys Res Commun. 1970 Jan 23;38(2):238–243. doi: 10.1016/0006-291x(70)90702-3. [DOI] [PubMed] [Google Scholar]
- McCarthy C. Utilization of palmitic acid by Mycobacterium avium. Infect Immun. 1971 Sep;4(3):199–204. doi: 10.1128/iai.4.3.199-204.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Middlebrook G., Coleman C. M., Schaefer W. B. SULFOLIPID FROM VIRULENT TUBERCLE BACILLI. Proc Natl Acad Sci U S A. 1959 Dec;45(12):1801–1804. doi: 10.1073/pnas.45.12.1801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Migliore D., Augier J., Boisvert H., Jollès P. Wax D from different bovine strains of Mycobacterium. J Bacteriol. 1971 Aug;107(2):548–550. doi: 10.1128/jb.107.2.548-550.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Migliore D., Jolles P. Contribution to the study of the structure of adjuvant active waxes D from mycobacteria: Isolation of a peptidoglycan. FEBS Lett. 1968 Nov;2(1):7–9. doi: 10.1016/0014-5793(68)80085-7. [DOI] [PubMed] [Google Scholar]
- Migliore D., Jollès P. Sur la structure chimique de la partie azotée des cires D de Mycobacterium tuberculosis, var. hominis. C R Acad Sci Hebd Seances Acad Sci D. 1969 Dec 3;269(22):2268–2270. [PubMed] [Google Scholar]
- Minnikin D. E., Polgar N. Studies on the mycolic acids from human tubercle bacilli. Tetrahedron Lett. 1966 Jun;23:2643–2647. doi: 10.1016/s0040-4039(01)84131-9. [DOI] [PubMed] [Google Scholar]
- Misaki A., Ikawa N., Kotani S., Kato T. Cell wall arabinogalactan of Mycobacterium phlei. Biochim Biophys Acta. 1970 Aug 14;215(2):405–408. doi: 10.1016/0304-4165(70)90040-1. [DOI] [PubMed] [Google Scholar]
- Misaki A., Yukawa S. Studies on cell walls of Mycobacteria. II. Constitution of polysaccharides from BCG cell walls. J Biochem. 1966 May;59(5):511–520. doi: 10.1093/oxfordjournals.jbchem.a128335. [DOI] [PubMed] [Google Scholar]
- Misaki A., Yukawa S., Tsuchiya K., Yamasaki T. Studies on cell walls of Mycobacteria. I. Chemical and biological properties of the cell walls and the mucopeptide of BCG. J Biochem. 1966 Apr;59(4):388–396. doi: 10.1093/oxfordjournals.jbchem.a128314. [DOI] [PubMed] [Google Scholar]
- Motomiya M., Mayama A., Fujimoto M., Sato H., Oka S. Chemistry and biology of phospholipids from an unclassified mycobacteria, P6. Chem Phys Lipids. 1969 Apr;3(2):159–167. doi: 10.1016/0009-3084(69)90007-3. [DOI] [PubMed] [Google Scholar]
- Murohashi T., Kondo E., Yoshida K. The role of lipids in acid-fastness of mycobacteria. Am Rev Respir Dis. 1969 May;99(5):794–798. doi: 10.1164/arrd.1969.99.5.794. [DOI] [PubMed] [Google Scholar]
- Murohashi T., Yoshida K. Biology of the mycobacterioses. Biological significance of acid-fastness of mycobacteria. Ann N Y Acad Sci. 1968 Sep 5;154(1):58–67. doi: 10.1111/j.1749-6632.1968.tb16695.x. [DOI] [PubMed] [Google Scholar]
- Murohashi T., Yoshida K. Effect of ultraviolet irradiation on the acid-fastness of drug-resistant mutants of tubercle bacilli, with special reference to the virulence of isoniazid-resistant strains. Am Rev Respir Dis. 1968 Feb;97(2):283–291. doi: 10.1164/arrd.1968.97.2.283. [DOI] [PubMed] [Google Scholar]
- Murthy H. S., Kumar K. S., Venkitasubramanian NAD- and NADP-specific dehydrogenases in cord-factor-treated mice. Biochim Biophys Acta. 1967;146(2):584–588. doi: 10.1016/0005-2744(67)90243-4. [DOI] [PubMed] [Google Scholar]
- NOLL H., BLOCH H., ASSELINEAU J., LEDERER E. The chemical structure of the cord factor of Mycobacterium tuberculosis. Biochim Biophys Acta. 1956 May;20(2):299–309. doi: 10.1016/0006-3002(56)90289-x. [DOI] [PubMed] [Google Scholar]
- NOLL H. The chemistry of cord factor, a toxic glycolipid of M. tuberculosis. Bibl Tuberc. 1956;(10):149–183. [PubMed] [Google Scholar]
- Nojima S., Kataoka T., Inoue K. Haptenic activity of phospholipids. Jpn J Med Sci Biol. 1970 Apr;23(2):129–129. [PubMed] [Google Scholar]
- Oka S., Fukushi K., Fujimoto M., Sato H., Motomiya M. La distribution subcellulaire des phospholipides de la Mycobactérie. C R Seances Soc Biol Fil. 1968;162(8):1648–1650. [PubMed] [Google Scholar]
- Okuyama H., Kankura T., Nojima S. Positional distribution of fatty acids in phospholipids from Mycobacteria. J Biochem. 1967 Jun;61(6):732–737. doi: 10.1093/oxfordjournals.jbchem.a128607. [DOI] [PubMed] [Google Scholar]
- Ono Y., Nojima S. Phospholipase A of Mycobacterium phlei: a regulatory membrane enzyme with ferric iron as effector. J Biochem. 1969 Jun;65(6):979–981. doi: 10.1093/oxfordjournals.jbchem.a129106. [DOI] [PubMed] [Google Scholar]
- Ono Y., Nojima S. Phospholipases of the membrane fraction of Mycobacterium phlei. Biochim Biophys Acta. 1969 Jan 21;176(1):111–119. [PubMed] [Google Scholar]
- PEARSON C. M. EXPERIMENTAL JOINT DISEASE OBSERVATIONS ON ADJUVANT-INDUCED ARTHRITIS. J Chronic Dis. 1963 Aug;16:863–874. doi: 10.1016/0021-9681(63)90136-x. [DOI] [PubMed] [Google Scholar]
- PEARSON C. M., WAKSMAN B. H., SHARP J. T. Studies of arthritis and other lesions induced in rats by injection of mycobacterial adjuvant. V. Changes affecting the skin and mucous membranes. Comparison of the experimental process with human disease. J Exp Med. 1961 Mar 1;113:485–510. doi: 10.1084/jem.113.3.485. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PIERARD A., GOLDMAN D. S. Enzyme systems in the mycobacteria. 14. Fatty acid synthesis in cell-free extracts of Mycobacterium tuberculosis. Arch Biochem Biophys. 1963 Jan;100:56–65. doi: 10.1016/0003-9861(63)90034-1. [DOI] [PubMed] [Google Scholar]
- Pangborn M. C. Biology of the mycobacterioses. Structure of mycobacterial phosphatides. Ann N Y Acad Sci. 1968 Sep 5;154(1):133–139. doi: 10.1111/j.1749-6632.1968.tb16703.x. [DOI] [PubMed] [Google Scholar]
- Pangborn M. C., McKinney J. A. Purification of serologically active phosphoinositides of Mycobacterium tuberculosis. J Lipid Res. 1966 Sep;7(5):627–633. [PubMed] [Google Scholar]
- Pigretti M., Vilkas E., Lederer E., Bloch H. Propriétés chimiques et biologiques de fractions phosphatidiques isolées de "l'antigène méthylique" de Mycobacterium tuberculosis. Bull Soc Chim Biol (Paris) 1965;47(11):2039–2046. [PubMed] [Google Scholar]
- Ribi E., Brehmer W., Milner K. C., Wicht W. C. Specific and nonspecific stimulation of resistance in mice aganist infection with Mycobacterium tuberculosis H37Rv. Pneumonologie. 1970;142(2):264–273. doi: 10.1007/BF02095224. [DOI] [PubMed] [Google Scholar]
- Ribi E. Currents in tuberculosis research. J Infect Dis. 1971 May;123(5):562–565. doi: 10.1093/infdis/123.5.562. [DOI] [PubMed] [Google Scholar]
- SMITH D. W., HARRELL W. K., RANDALL H. M. Correlation of biologic properties of strains of Mycobacterium with their infrared spectrums. III. Differentiation of bovine and human varieties of M. tuberculosis by means of their infrared spectrums. Am Rev Tuberc. 1954 Apr;69(4):505–510. doi: 10.1164/art.1954.69.4.505. [DOI] [PubMed] [Google Scholar]
- SMITH D. W., RANDALL H. M., GASTAMBIDE-ODIER M. M., KOEVOET A. L. The characterization of mycobacterial strains by the composition of their lipide extracts. Ann N Y Acad Sci. 1957 Sep 7;69(1):145–157. doi: 10.1111/j.1749-6632.1957.tb49655.x. [DOI] [PubMed] [Google Scholar]
- SMITH D. W., RANDALL H. M., MACLENNAN A. P., LEDERER E. Mycosides: a new class of type-specific glycolipids of Mycobacteria. Nature. 1960 Jun 11;186:887–888. doi: 10.1038/186887a0. [DOI] [PubMed] [Google Scholar]
- STEWART-TULL D. E., WHITE R. G. THE OCCURRENCE OF MURAMIC ACID IN WAX D PREPARATIONS OF MYCOBACTERIA. J Gen Microbiol. 1964 Jan;34:43–49. doi: 10.1099/00221287-34-1-43. [DOI] [PubMed] [Google Scholar]
- STINEBRING W. R., YOUNGNER J. S. PATTERNS OF INTERFERON APPEARANCE IN MICE INFECTED WITH BACTERIA OR BACTERIAL ENDOTOXIN. Nature. 1964 Nov 14;204:712–712. doi: 10.1038/204712a0. [DOI] [PubMed] [Google Scholar]
- Saier M. H., Jr, Ballou C. E. The 6-O-methylglucose-containig lipopolysaccharide of Mycobacterium phlei. Complet structure of the polysaccharide. J Biol Chem. 1968 Aug 25;243(16):4332–4341. [PubMed] [Google Scholar]
- Saier M. H., Jr, Ballou C. E. The 6-O-methylglucose-containing lipopolysaccharide of Mycobacterium phlei. Identification of D-glyceric acid and 3-O-methyl-D-glucose in the polysaccharide. J Biol Chem. 1968 Mar 10;243(5):992–1005. [PubMed] [Google Scholar]
- Saier M. H., Jr, Ballou C. E. The 6-O-methylglucose-containing lipopolysaccharide of Mycobacterium phlei. Structure of the reducing end of the polysaccharide. J Biol Chem. 1968 Aug 25;243(16):4319–4331. [PubMed] [Google Scholar]
- Sarma G. R., Chandramouli V., Venkitasubramanian T. A. Occurrence of phosphonolipids in mycobacteria. Biochim Biophys Acta. 1970 Dec 15;218(3):561–563. [PubMed] [Google Scholar]
- Schaefer W. B., Lewis C. W., Jr Effect of oleic acid on growth and cell structure of mycobacteria. J Bacteriol. 1965 Nov;90(5):1438–1447. doi: 10.1128/jb.90.5.1438-1447.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scher M., Lennarz W. J. Studies on the biosynthesis of mannan in Micrococcus lysodeikticus. I. Characterization of mannan-14C formed enzymatically from mannosyl-1-phosphoryl-undecaprenol. J Biol Chem. 1969 May 25;244(10):2777–2789. [PubMed] [Google Scholar]
- Schubert K., Rose G., Wachtel H., Hörhold C., Ikekawa N. Zum Vorkommen von Sterinen in Bakterien. Eur J Biochem. 1968 Jul;5(2):246–251. doi: 10.1111/j.1432-1033.1968.tb00364.x. [DOI] [PubMed] [Google Scholar]
- Senn M., Ioneda T., Pudles J., Lederer E. Spectrométrie de masse de glycolipides. I. Structure du "cord factor" de Corynebacterium diphtheriae. Eur J Biochem. 1967 May;1(3):353–356. doi: 10.1111/j.1432-1033.1967.tb00081.x. [DOI] [PubMed] [Google Scholar]
- Shankaran R., Venkitasubramanian T. A. Effect of cord factor on carbohydrate metabolism in mice. Am Rev Respir Dis. 1970 Mar;101(3):401–407. doi: 10.1164/arrd.1970.101.3.401. [DOI] [PubMed] [Google Scholar]
- Subrahmanyam D., Singhvi D. R. Phosphatide antigens of mycobacteria. Proc Soc Exp Biol Med. 1965 Oct;120(1):102–105. doi: 10.3181/00379727-120-30456. [DOI] [PubMed] [Google Scholar]
- TAKAHASHI Y. Specific serum agglutination of kaolin particles sensitized with tubercle phosphatide and its clinical evaluation as a serodiagnostic test for tuberculosis. Am Rev Respir Dis. 1962 May;85:708–719. doi: 10.1164/arrd.1962.85.5.708. [DOI] [PubMed] [Google Scholar]
- TANAKA A., KITAGAWA M. FRACTIONATION AND CHARACTERIZATION OF WAX D, A MACROMOLECULAR PEPTIDOGLYCOLIPID OF MYCOBACTERIUM TUBERCULOSIS. I. BIOCHEMICAL INVESTIGATIONS OF WAX D OF HUMAN STRAIN H37RA. Biochim Biophys Acta. 1965 Feb 1;98:182–193. [PubMed] [Google Scholar]
- Takayama K., David H. L., Wang L., Goldman D. S. Isolation and characterization of uridine diphosphate-N-glycolylmuramyl-L-alanyl-gamma-D-glutamyl-meso-alpha,alpha'-diaminopimelic acid from Mycobacterium tuberculosis. Biochem Biophys Res Commun. 1970 Apr 8;39(1):7–12. doi: 10.1016/0006-291x(70)90749-7. [DOI] [PubMed] [Google Scholar]
- Takayama K., Goldman D. S. Enzymatic synthesis of mannosyl-1-phosphoryl-decaprenol by a cell-free system of Mycobacterium tuberculosis. J Biol Chem. 1970 Dec 10;245(23):6251–6257. [PubMed] [Google Scholar]
- Takayama K., Goldman D. S. Pathway for the synthesis of mannophospholipids in Mycobacterium tuberculosis. Biochim Biophys Acta. 1969 Jan 21;176(1):196–198. doi: 10.1016/0005-2760(69)90089-7. [DOI] [PubMed] [Google Scholar]
- Tanaka A., Anaka K., Hagimoto D., Sugiyama K. Quantitative relationship for adjuvanticity between antigen and adjuvant. Int Arch Allergy Appl Immunol. 1967;32(2):224–235. doi: 10.1159/000229931. [DOI] [PubMed] [Google Scholar]
- Tanaka A., Hirota N., Sugiyama K. Antigenicity of wax D, a peptidoglycolipid of M. tuberculosis. 3. Prliminary report on the clinical evaluation of wax D agglutination as a sero-diagnostic test for pulmonary tuberculosis. Int Arch Allergy Appl Immunol. 1967;32(3):349–352. [PubMed] [Google Scholar]
- Tanaka A., Ishibashi T., Koga T., Takamoto M., Kohashi O. Adjuvant effect and structure of wax D, a lipopolysaccharide of M. tuberculosis. Jpn J Med Sci Biol. 1970 Apr;23(2):128–128. [PubMed] [Google Scholar]
- Tanaka A., Ishibashi T., Sugiyama K. Antigenicity of wax D, a peptidoglycolipid of M. tuberculosis. II. Relationship between antigenicity and chemical structures. Int Arch Allergy Appl Immunol. 1967;32(2):215–223. doi: 10.1159/000229930. [DOI] [PubMed] [Google Scholar]
- Tanaka A., Tanaka K., Tsubone T., Kuroda Y., Sugiyama K. Fractionation and characterization of wax D, a peptidoglycolipid of Mycobacterium tuberculosis. II Adjuvanticity of the subfractions of wax D of H37Ra and wax D of other strains M. tuberculosis. Int Arch Allergy Appl Immunol. 1965;28(6):340–352. doi: 10.1159/000229680. [DOI] [PubMed] [Google Scholar]
- Tanaka K., Tanaka A., Sugiyama K. Immunological adjuvants. I. Adjuvant activity and immunogenicity of acetylated wax D and its subfractions. Int Arch Allergy Appl Immunol. 1968;34(5):495–506. [PubMed] [Google Scholar]
- Thomas D. W., Das B. C., Géro S. D., Lederer E. Advantages and limitations of the mass spectrometric sequence determination of permethylated oligopeptide derivatives. Biochem Biophys Res Commun. 1968 Jul 26;32(2):199–207. doi: 10.1016/0006-291x(68)90369-0. [DOI] [PubMed] [Google Scholar]
- Tokunaga T., Kataoka T., Suga K. Phage inactivation by an ethanol-ether extract of Mycobacterium smegmatis. Am Rev Respir Dis. 1970 Feb;101(2):309–313. doi: 10.1164/arrd.1970.101.2.309. [DOI] [PubMed] [Google Scholar]
- Vilkas E., Delaumeny J. M., Nacasch C. Sur la structure du polysaccharide des Cires D d'une souche humaine virulente de Mycobacterium tuberculosis. Biochim Biophys Acta. 1968 Apr 16;158(1):147–150. [PubMed] [Google Scholar]
- Vilkas E., Lederer E. N-methylation de peptides par a methode de Hakomori. Structure du mycoside Cbl. Tetrahedron Lett. 1968 May;(26):3089–3092. doi: 10.1016/s0040-4039(00)89603-3. [DOI] [PubMed] [Google Scholar]
- Vilkas E., Markovits J. Isolement d'un digalactoside et d'un mycolate de diarabinoside a partir de cires d d'une souche humaine virulente de Mycobacterium tuberculosis. FEBS Lett. 1968 Nov;2(1):20–22. doi: 10.1016/0014-5793(68)80089-4. [DOI] [PubMed] [Google Scholar]
- Voiland A., Bruneteau M., Michel G. Etude du mycoside C 2 de Mycobacterium avium. Détermination de la structure. Eur J Biochem. 1971 Jul 29;21(2):285–291. doi: 10.1111/j.1432-1033.1971.tb01468.x. [DOI] [PubMed] [Google Scholar]
- WHITE R. G., BERNSTOCK L., JOHNS R. G., LEDERER E. The influence of components of M. tuberculosis and other Mycobacteria upon antibody production to ovalbumin. Immunology. 1958 Jan;1(1):54–66. [PMC free article] [PubMed] [Google Scholar]
- WHITE R. G., COONS A. H., CONNOLLY J. M. Studies on antibody production. IV. The role of a wax fraction of Mycobacterium tuberculosis in adjuvant emulsions on the production of antibody to egg albumin. J Exp Med. 1955 Jul 1;102(1):83–104. doi: 10.1084/jem.102.1.83. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WHITE R. G., JOLLES P., SAMOUR D., LEDERER E. CORRELATION OF ADJUVANT ACTIVITY AND CHEMICAL STRUCTURE OF WAX D FRACTIONS OF MYCOBACTERIA. Immunology. 1964 Mar;7:158–171. [PMC free article] [PubMed] [Google Scholar]
- WINDMAN I., ARTMAN M., BEKIERKUNST A. TISSUE METABOLISM IN INFECTION. LIVER MICROSOMAL ENZYMES OF MICE AND GUINEA PIGS IN EXPERIMENTAL TUBERCULOSIS. Am Rev Respir Dis. 1965 May;91:706–712. doi: 10.1164/arrd.1965.91.5.706. [DOI] [PubMed] [Google Scholar]
- Walczak E., Etémadi A. H. Sur la structure et la biogenèse des acides alpha-avimycoliques de Mycobacterium avium. C R Acad Sci Hebd Seances Acad Sci D. 1965 Oct 4;261(14):2771–2774. [PubMed] [Google Scholar]
- Walker R. W., Barakat H., Hung J. G. The positional distribution of fatty acids in the phospholipids and triglycerides of Mycobacterium smegmatis and M. bovis BCG. Lipids. 1970 Aug;5(8):684–691. doi: 10.1007/BF02531435. [DOI] [PubMed] [Google Scholar]
- Wang L., Kusaka T., Goldman D. S. Elongation of fatty acids in Mycobacterium tuberculosis. J Bacteriol. 1970 Mar;101(3):781–785. doi: 10.1128/jb.101.3.781-785.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- White R. G. Role of adjuvants in the production of delayed hypersensitivity. Br Med Bull. 1967 Jan;23(1):39–45. doi: 10.1093/oxfordjournals.bmb.a070514. [DOI] [PubMed] [Google Scholar]
- Wietzerbin-Falszpan J., Das B. C., Azuma I., Adam A., Petit J. F., Lederer E. Isolation and mass spectrometric identification of the peptide subunits of mycobacterial cell walls. Biochem Biophys Res Commun. 1970 Jul 13;40(1):57–63. doi: 10.1016/0006-291x(70)91045-4. [DOI] [PubMed] [Google Scholar]
- Winder F. G., Collins P. B. Inhibition by isoniazid of synthesis of mycolic acids in Mycobacterium tuberculosis. J Gen Microbiol. 1970 Sep;63(1):41–48. doi: 10.1099/00221287-63-1-41. [DOI] [PubMed] [Google Scholar]
- Winder F. G., Rooney S. A. The effects of isoniazid on the carbohydrates of Mycobacterium tuberculosis BCG. Biochem J. 1970 Apr;117(2):355–368. doi: 10.1042/bj1170355. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wood F. D., Pearson C. M., Tanaka A. Capacity of mycobacterial wax D and its subfractions to induce adjuvant arthritis in rats. Int Arch Allergy Appl Immunol. 1969;35(5):456–467. doi: 10.1159/000230198. [DOI] [PubMed] [Google Scholar]
- Yamamoto K., Anacker R. L., Ribi E. Macrophage Migration Inhibition Studies with Cells from Mice Vaccinated with Cell Walls of Mycobacterium bovis BCG: Relationship Between Inhibitory Activity of Lung Cells and Resistance to Airborne Challenge with Mycobacterium tuberculosis H37Rv. Infect Immun. 1970 Jun;1(6):595–599. doi: 10.1128/iai.1.6.595-599.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yamamura Y., Onoue K., Azuma I. Biology of the mycobacterioses. Chemical and immunological studies on peptides and polysaccharides from tubercle bacilli. Ann N Y Acad Sci. 1968 Sep 5;154(1):88–97. doi: 10.1111/j.1749-6632.1968.tb16698.x. [DOI] [PubMed] [Google Scholar]
- Yano I., Kusunose M. Propionate incorporation into mycocerosic acid by resting cells of Mycobacterium tuberculosis bovis. Biochim Biophys Acta. 1966 Jun 1;116(3):593–596. [PubMed] [Google Scholar]
- Youmans A. S., Youmans G. P. Factors affecting immunogenic activity of mycobacterial ribosomal and ribonucleic acid preparations. J Bacteriol. 1969 Jul;99(1):42–50. doi: 10.1128/jb.99.1.42-50.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Youmans G. P., Youmans A. S. Recent studies on acquired immunity in tuberculosis. Curr Top Microbiol Immunol. 1969;48:129–178. doi: 10.1007/978-3-642-46163-7_6. [DOI] [PubMed] [Google Scholar]