Literature DB >> 24442701

Inverse dark reversion of phytochrome: An explanation.

R E Kendrick1, C J Spruit.   

Abstract

Pea epicotyl tissue freeze dried with phytochrome (P) in the red absorbing (Pr) form, on exposure to red light does not form the far-red absorbing form of P (Pfr), but forms the intermediate P698 which reverts to Pr in darkness. Similar tissue containing the pigment as Pfr undergoes a photoreversible reaction on exposure to alternate red and far-red light. This represents the photoreversibility between Pfr and the intermediate P650. The difference spectrum of this reaction is similar to that of phytochrome photoconversion in dry cucumber seeds. P650 is shown to revert slowly to Pfr in darkness and it is proposed that this reaction accounts for the observation of apparent inverse dark reversion in cucumber seeds. Partial rehydration of freeze-dried tissue containing Pr, by means of 80% glycerol: 20% water (v/v), partially restores photoreversibility between Pr and Pfr. In such samples Pfr formation from intermediates, however, is slow and continues for several min in the dark after exposure to red light. This reaction can simulate the apparent inverse dark reversion observed in many seeds during early stages of imbibition. In this case Pfr appears from an intermediate produced by exposure to red light, which has not had time to form Pfr during the normal assay period. These two processes of Pfr production from intermediates in darkness, present under conditionsof partial or extreme dehydration, can explain previous experimental observations interpreted as inverse dark reversion.It is therefore proposed that the process, formerly described as 'inverse dark reversion', is not a transformation of Pr to Pfr and that there is not a separate form of phytochrome responsible for this reaction.

Entities:  

Year:  1974        PMID: 24442701     DOI: 10.1007/BF00390294

Source DB:  PubMed          Journal:  Planta        ISSN: 0032-0935            Impact factor:   4.116


  10 in total

1.  Phytochrome properties and the molecular environment.

Authors:  R E Kendrick; C J Spruit
Journal:  Plant Physiol       Date:  1973-10       Impact factor: 8.340

2.  Nonphotochemical Transformations of Phytochrome in Vivo.

Authors:  W L Butler; H C Lane; H W Siegelman
Journal:  Plant Physiol       Date:  1963-09       Impact factor: 8.340

3.  Phytochrome in Embryos of Pinus palustris.

Authors:  E M Tobin; W R Briggs
Journal:  Plant Physiol       Date:  1969-01       Impact factor: 8.340

4.  Phytochrome in seeds of Amaranthus caudatus.

Authors:  R E Kendrick; C J Spruit; B Frankland
Journal:  Planta       Date:  1969-12       Impact factor: 4.116

5.  Phytochrome in cucumber seeds.

Authors:  C J Spruit; A L Mancinelli
Journal:  Planta       Date:  1969-12       Impact factor: 4.116

6.  Phytochrome appearance and distribution in the embryonic axis and seedling of Alaska peas.

Authors:  J A McArthur; W R Briggs
Journal:  Planta       Date:  1970-06       Impact factor: 4.116

7.  The role of hydration in the phototransformation of phytochrome.

Authors:  E M Tobin; W R Briggs; P K Brown
Journal:  Photochem Photobiol       Date:  1973-12       Impact factor: 3.421

8.  Low-temperature action spectra for transformations of photoperiodic pigments.

Authors:  C J Spruit
Journal:  Biochim Biophys Acta       Date:  1966-07-13

9.  Photocontrol of germination in Amaranthus caudatus.

Authors:  R E Kendrick; B Frankland
Journal:  Planta       Date:  1969-12       Impact factor: 4.116

10.  Properties of phytochrome in gymnosperms.

Authors:  R Grill; C J Spruit
Journal:  Planta       Date:  1972-09       Impact factor: 4.116

  10 in total
  2 in total

1.  Phytochrome intermediates in freeze-dried tissue.

Authors:  C J Spruit; R E Kendrick; R J Cooke
Journal:  Planta       Date:  1975-01       Impact factor: 4.116

2.  Phytochrome-mediated germination control of maize caryopses.

Authors:  C A Thanos; K Mitrakos
Journal:  Planta       Date:  1979-09       Impact factor: 4.116

  2 in total

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