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Biosynthesis of Arginine in L Cells Infected with Chlamydiae
Author(s) -
Mary W. Treuhaft,
James W. Moulder
Publication year - 1968
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.96.6.2004-2011.1968
Subject(s) - chlamydiae , biology , arginine , chlamydia psittaci , ornithine , microbiology and biotechnology , strain (injury) , titer , virology , biochemistry , chlamydia trachomatis , amino acid , chlamydia , immunology , virus , anatomy
Three members of the genusChlamydia were examined for their ability to synthesize arginine, an ability their L cell (mouse fibroblasts) hosts lacked.C. psittaci (strain 6BC) multiplied in arginine-free medium 199 without significant decrease in titer and incroporated14 C-glutamate and14 C-ornithine into the arginine fraction of its protein. In arginine-free media,C. trachomatis (strain mouse pneumonitis) andC. psittaci (strain meningopneumonitis) grew to only 1 to 10% of the titer obtained in arginine-containing media. The decreased ability of these two strains to multiply in arginine-free media was paralleled by a decreased ability of infected host cells to incorporate14 C-glutamate into protein arginine. These results suggest that chlamydiae either synthesize arginine themselves, or, in some unknown manner, cause their host cells to do so.

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