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. 1964 Apr 1;21(1):27–33. doi: 10.1083/jcb.21.1.27

FACTORS AFFECTING THE INTRACELLUALR SYNTHESIS OF KYNURENINE

T M Rizki 1, Rose M Rizki 1
PMCID: PMC2106422  PMID: 14154493

Abstract

Near the time of pupation, autofluorescent kynurenine globules appear in the cells in the anterior region of the fatbody of Drosophila melanogaster. It has been reported previously that kynurenine synthesis may be induced in an additional group of fat cells by feeding the precursor tryptophan to Drosophila larvae, and that this induction of kynurenine production viewed within the fat cells is correlated with an increase in tryptophan pyrrolase activity. In the present report, conditions are outlined which result in the appearance of kynurenine in all of the fat cells. The number of cells in the fatbody which contain kynurenine is influenced by the quantity of tryptophan included in the diet, as well as by the developmental stage at the time of treatment and the duration of the feeding period on the inducer. Physical barriers modifying permeability, such as the membranous layer noted surrounding the fatbody, may be a factor in the regulation of the time and nature of the cellular induction of kynurenine synthesis. Another factor to be considered is the possibility of interference with the availability of tryptophan as a substrate or inducer for this synthesis within the cell. It is suggested that the occurrence of pteridines in some of the fat cells may modify the response of these cells to produce kynurenine, since pteridines as electron acceptors can complex with tryptophan as an electron donor. Kynurenine may be produced in the fat cells under in vitro conditions when they are incubated with L-tryptophan, but kynurenine is not formed when fat cells are incubated with D-tryptophan. The in vitro studies further demonstrate that induction of kynurenine synthesis may occur in fat cells isolated from young larvae in contrast, to in vivo conditions in which inducer does not effect an earlier appearance of kynurenine in the larval fatbody.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Fujimori E. INTERACTION BETWEEN PTERIDINES AND TRYPTOPHAN. Proc Natl Acad Sci U S A. 1959 Feb;45(2):133–136. doi: 10.1073/pnas.45.2.133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Isenberg I., Szent-Györgyi A. FREE RADICAL FORMATION IN RIBOFLAVIN COMPLEXES. Proc Natl Acad Sci U S A. 1958 Sep 15;44(9):857–862. doi: 10.1073/pnas.44.9.857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. PITOT H. C., CHO Y. S. Studies on the mechanism of enzyme induction in rat liver. Cold Spring Harb Symp Quant Biol. 1961;26:371–377. doi: 10.1101/sqb.1961.026.01.046. [DOI] [PubMed] [Google Scholar]
  4. Pullman B., Pullman A. ELECTRON-DONOR AND -ACCEPTOR PROPERTIES OF BIOLOGICALLY IMPORTANT PURINES, PYRIMIDINES, PTERIDINES, FLAVINS, AND AROMATIC AMINO ACIDS. Proc Natl Acad Sci U S A. 1958 Dec 15;44(12):1197–1202. doi: 10.1073/pnas.44.12.1197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. RIZKI M. T. Melanotic tumor ormation in Drosophila. J Morphol. 1960 Mar;106:147–157. doi: 10.1002/jmor.1051060203. [DOI] [PubMed] [Google Scholar]
  6. RIZKI T. M. Genetic control of cytodifferentiation. J Cell Biol. 1963 Mar;16:513–520. doi: 10.1083/jcb.16.3.513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. RIZKI T. M., RIZKI R. M. An inducible enzyme system in the larval cells of Drosophila melanogaster. J Cell Biol. 1963 Apr;17:87–92. doi: 10.1083/jcb.17.1.87. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. RIZKI T. M., RIZKI R. M. Cytodifferentiation in the rosy mutant of Drosophila melanogaster. J Cell Biol. 1962 Jan;12:149–157. doi: 10.1083/jcb.12.1.149. [DOI] [PMC free article] [PubMed] [Google Scholar]

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