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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1981 Feb;78(2):1009–1013. doi: 10.1073/pnas.78.2.1009

Blue-light receptor in a white mutant of Physarum polycephalum mediates inhibition of spherulation and regulation of glucose metabolism.

T Schreckenbach, B Walckhoff, C Verfuerth
PMCID: PMC319935  PMID: 6940119

Abstract

Blue light induces sporulation of Physarum polycephalum macroplasmodia and reversibly inhibits spherulation (sclerotization) of microplasmodia. Illuminated microplasmodia have an abnormal appearance. The photobiological responses of the plasmodia appear to be unaffected by the absence of yellow pigment in the white mutant strain used. Illumination of microplasmodial suspensions with blue light (lambda max approximately 465 nm) results also in an early effect on glucose metabolism: glucose consumption is reversibly inhibited. By using radioactive glucose it was shown that the main products formed are a water-insoluble glucan and the disaccharide trehalose. Inhibition of glucose consumption in the light results in decreased production of these two compounds. Illumination of microplasmodial suspensions also causes a reversible effect on the pH of the medium which is interpreted as a decreased production of a yet unidentified acid from glucose. The action spectrum of the light-induced pH response shows maxima near 390, 465, and 485 nm. It resembles the absorption spectrum of a flavoprotein and confirms the existence of a blue-light receptor in P. polycephalum microplasmodia.

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Selected References

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

  1. Daniel J. W., Eustace J. The effect of light on the permeability of a myxomycete. FEBS Lett. 1972 Oct 1;26(1):327–332. doi: 10.1016/0014-5793(72)80604-5. [DOI] [PubMed] [Google Scholar]
  2. Goodman E. M., Rusch H. P. Ultrastructural changes during spherule formation in Physarum polycephalum. J Ultrastruct Res. 1970 Jan;30(1):172–183. doi: 10.1016/s0022-5320(70)90071-7. [DOI] [PubMed] [Google Scholar]
  3. McCormick J. J., Blomquist J. C., Rusch H. P. Isolation and Characterization of a Galactosamine Wall from Spores and Spherules of Physarum polycephalum. J Bacteriol. 1970 Dec;104(3):1119–1125. doi: 10.1128/jb.104.3.1119-1125.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. NAKAMURA S., WAKEYAMA T. Distribution of trypsin inhibitors in the sera of various animals. Nature. 1961 Dec 16;192:1077–1077. doi: 10.1038/1921077a0. [DOI] [PubMed] [Google Scholar]
  5. Sussman A. S., Lingappa B. T. Role of Trehalose in Ascospores of Neurospora Tetrasperma. Science. 1959 Nov 13;130(3385):1343–1343. doi: 10.1126/science.130.3385.1343. [DOI] [PubMed] [Google Scholar]
  6. Takasaki S., Kobata A. Microdetermination of sugar composition by radioisotope labeling. Methods Enzymol. 1978;50:50–54. doi: 10.1016/0076-6879(78)50006-2. [DOI] [PubMed] [Google Scholar]
  7. Wormington W. M., Cho C. G., Weaver R. F. Sporulation-inducing factor in slime mould Physarum polycephalum. Nature. 1975 Jul 31;256(5516):413–414. doi: 10.1038/256413a0. [DOI] [PubMed] [Google Scholar]
  8. Wormington W. M., Weaver R. F. Photoreceptor pigment that induces differentiation in the slime mold Physarum polycephalum. Proc Natl Acad Sci U S A. 1976 Nov;73(11):3896–3899. doi: 10.1073/pnas.73.11.3896. [DOI] [PMC free article] [PubMed] [Google Scholar]

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