1968
DOI: 10.1104/pp.43.6.941
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Amino Acid Incorporation in Developing Fucus Embryos

Abstract: Abstract. The incorporation of 14C-leucine and 14C-amino acid mixture into protein in unfertilized eggs and developing embryos of the brown alga Fucus vesiculosus L. was studied. Bacterial contamination was initially a problem, but it was found that the addition of 40 jug/ml chloramphenicol to the incubation medium would inhibit bacterial protein synthesis without affecting early development of the Fucus embryos. The kinetics of uptake and incorporation of 14C-leucine into the trichloroacetic acid-soluble and … Show more

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Cited by 20 publications
(3 citation statements)
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“…Although bacterial 'contamination' has been mentioned previously in an experiment with eggs and embryos of Fucus vesiculosus (Peterson & Torrey 1968), this is the first direct observation of bacteria over the surface of oogonia at the moment of their release from conceptacle (Fig. 2).…”
Section: Introductionsupporting
confidence: 51%
“…Although bacterial 'contamination' has been mentioned previously in an experiment with eggs and embryos of Fucus vesiculosus (Peterson & Torrey 1968), this is the first direct observation of bacteria over the surface of oogonia at the moment of their release from conceptacle (Fig. 2).…”
Section: Introductionsupporting
confidence: 51%
“…This data and the elegant demonstration by Jaffe (33) that polarized light produces bipolar embryos, argues strongly for a polar axis which is initially labile and "arises in some more epigenetic manner than through the directed rotation of some preformed asymmetric structure." Postfertilization RNA and protein synthesis (72,77), as well as the acquisition of a sufficient pressure potential for rhizoid elongation (3,80), are also required for polar embryo formation.…”
Section: Fucusdevelopmentmentioning
confidence: 99%
“…A method based on that of Peterson & Torrey (1968) was used for effecting gamete liberation in the dioecious species F. vesiculosus and F. serratus. The female receptacles were placed in sterile sea water in covered crystallizing dishes overnight at 10°C, 7.5 W m -a irradiance, and 16:g photoperiod for oosphere release to occur.…”
Section: Release Of Gametesmentioning
confidence: 99%