1981
DOI: 10.1111/j.1399-3054.1981.tb00887.x
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Cellular changes during boron‐deficient culture of the diatom Cylindrotheca fusiformis

Abstract: The effects of boron‐deficient culture were studied on the unicellular diatom. Cylindrotheca fusiformis Reimann and Lewin. After 24 to 30 h, cell division was almost completely inhibited in boron‐deficient cultures. By 48 h of culture, boron‐deficient diatoms had approximately twice the modal cell volume of control cells, and at least twice the amount of organic constituents such as protein (2.0x), insoluble carbohydrate (2.4x), total phenols (2.6x), and chlorophyll at (2.1x). Boron deficiency led to irreversi… Show more

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Cited by 50 publications
(23 citation statements)
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“…Smyth and Dugger (21), using the diatom Cylindroteca fusiformis, explained this accumulation by photosynthetic enhancement in B-deficient cultures. This explanation is not valid in Anabaena.…”
Section: Discussionmentioning
confidence: 99%
“…Smyth and Dugger (21), using the diatom Cylindroteca fusiformis, explained this accumulation by photosynthetic enhancement in B-deficient cultures. This explanation is not valid in Anabaena.…”
Section: Discussionmentioning
confidence: 99%
“…Since then, B was shown to be essential for diatoms (Smyth and Dugger, 1981) and cyanobacteria (Bonilla et al, 1990) as well as for animals, including zebra fish (Danio rerio) (Rowe and Eckhert, 1999), trout (Oncorhynchus mykiss) (Eckhert, 1998;Rowe et al, 1998), frogs (Xenopus laevis) (Fort et al, 1998), and mice (Mus musculus) (Lanoue et al, 2000). Although the precise physiological role of B has not been established, it is beneficial for human health (Nielsen, 2000).…”
Section: Introductionmentioning
confidence: 99%
“…The algal cells (POC fraction), which were disrupted by a sonic probe, and the supernatants (Colloidal-OC fraction), which were extracted with EDTA solution, were assayed for presence of the intracellular enzyme glucose-6-phosphate dehydrogenase (GGPD, EC 1.1.1.49) activity using the method of Smyth & Dugger (1981), to determine the extent of contamination of the extraceilular polymer by intracellular material. Protein in the algal cells and the supernatant was measured by the method of Smyth & Dugger (1981) and the Bradford method (Bradford 1976).…”
mentioning
confidence: 99%