scholarly journals Rapid colour changes in Euglena sanguinea (Euglenophyceae) caused by internal lipid globule migration

2018 ◽  
Vol 54 (1) ◽  
pp. 91-101 ◽  
Author(s):  
Aitor Laza-Martínez ◽  
Beatriz Fernández-Marín ◽  
José Ignacio García-Plazaola
Keyword(s):  
2009 ◽  
Vol 57 (2) ◽  
pp. 231-237
Author(s):  
M. Zych ◽  
A. Stolarczyk ◽  
K. Maca ◽  
A. Banaś ◽  
K. Termińska-Pabis ◽  
...  

Differences in the assimilation of individual organic compounds (5 mM sugars and L-asparagine) under mixotrophic growth conditions were described for three naturally occurring Haematococcus strains.The effects of assimilation were measured by the growth intensity and size of algal cells, and the effect of colour changes in the cultures was observed. Some compounds caused the cell colouration to change from green to yellow, being the result of chlorophyll disappearance and the accumulation of yellow secondary carotenoids. In the present experiment none of the cultures turned red, thus excluding the intense accumulation of the commercially interesting carotenoid, astaxanthin.


Cells ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 835
Author(s):  
Selina Kiefer ◽  
Julia Huber ◽  
Hannah Füllgraf ◽  
Kristin Sörensen ◽  
Agnes Csanadi ◽  
...  

Pathological biopsy protocols require tissue marking dye (TMD) for orientation. In some cases (e.g., close margin), additional immunohistochemical analyses can be necessary. Therefore, the correlation between the applied TMD during macroscopy and the examined TMD during microscopy is crucial for the correct orientation, the residual tumour status and the subsequent therapeutic regime. In this context, our group observed colour changes during routine immunohistochemistry. Tissue specimens were marked with various TMD and processed by two different methods. TMD (blue, red, black, yellow and green) obtained from three different providers (A, B and C, and Whiteout/Tipp-Ex®) were used. Immunohistochemistry was performed manually via stepwise omission of reagents to identify the colour changing mechanism. Blue colour from provider A changed during immunohistochemistry into black, when 3,3′-Diaminobenzidine-tetrahydrochloride-dihydrate (DAB) and H2O2 was applied as an immunoperoxidase-based terminal colour signal. No other applied reagents, nor tissue texture or processing showed any influence on the colour. The remaining colours from provider A and the other colours did not show any changes during immunohistochemistry. Our results demonstrate an interesting and important pitfall in routine immunohistochemistry-based diagnostics that pathologists should be aware of. Furthermore, the chemical rationale behind the observed misleading colour change is discussed.


Sensors ◽  
2018 ◽  
Vol 18 (12) ◽  
pp. 4361
Author(s):  
Tinkara Mastnak ◽  
Aleksandra Lobnik ◽  
Gerhard Mohr ◽  
Matjaž Finšgar

The article presents naked-eye methods for fast, sensitive, and selective detection of isopentylamine and cadaverine vapours based on 4-N,N-dioctylamino-4′-dicyanovinylazobenzene (CR-528) and 4-N,N-dioctylamino-2′-nitro-4′-dicyanovinylazobenzene (CR-555) dyes immobilized in ethylene-vinyl acetate copolymer (EVA). The reaction of CR-528/EVA and CR-555/EVA indicator layers with isopentylamine vapours caused a vivid colour change from pink/purple to yellow/orange-yellow. Additionally, CR-555/EVA showed colour changes upon exposure to cadaverine. The colour changes were analysed by ultraviolet–visible (UV/VIS) molecular absorption spectroscopy for amine quantification, and the method was partially validated for the detection limit, sensitivity, and linear concentration range. The lowest detection limits were reached with CR-555/EVA indicator layers (0.41 ppm for isopentylamine and 1.80 ppm for cadaverine). The indicator layers based on EVA and dicyanovinyl azobenzene dyes complement the existing library of colorimetric probes for the detection of biogenic amines and show great potential for food quality control.


2016 ◽  
Vol 61 (sup2) ◽  
pp. 302-304 ◽  
Author(s):  
Hung-Wen Luo ◽  
Hung-Shing Chen ◽  
Ching-Ju Chou ◽  
Ming Ronnier Luo

2007 ◽  
Vol 42 (5) ◽  
pp. 369-384 ◽  
Author(s):  
Bruno Esteves ◽  
António Velez Marques ◽  
Idalina Domingos ◽  
Helena Pereira

2013 ◽  
Vol 129 (3) ◽  
pp. 223-231 ◽  
Author(s):  
Ozan Deveoglu ◽  
Gokhan Erkan ◽  
Emine Torgan ◽  
Recep Karadag
Keyword(s):  

1978 ◽  
Vol 56 (19) ◽  
pp. 2380-2404 ◽  
Author(s):  
D. J. S. Barr ◽  
V. E. Hadland-Hartmann

The zoospore ultrastructure of 12 species of Rhizophydium is described. Species include the following: R. chlorogonii (Serbinow) Jaczewski; R. constantineani Saccardo; R. haynaldii (Schaarschmidt) Fischer; R. capillaceum Barr; two morphologically and cytologically different species, each previously identified as R. sphaerotheca Zopf; R. patellarium Scholz; R. biporosum (Couch) Barr; R. subangulosum (Braun) Rabenhorst; R. laterale (Braun) Rabenhorst; R. sphaerocarpum (Zopf) Fischer var. spirogyrae Barr; and two isolates of R. pollinis-pini (Braun) Zopf. The Rhizophydium zoospore is basically similar to the Chytridium zoospore having (1) the nucleus, a compact cluster of ribosomes, one or more mitochondria, and a microbody – lipid globule complex compartmentalized into the core of the zoospore by a double membrane system and (2) two to five microtubules connecting one side of the kinetosome to the rumposome on the lipid globule surface and thus anchoring the lipid globule in a lateral–posterior position in the zoospore. Rhizophydium patellarium does not have kinetosome-associated microtubules or a rumposome but does have the membrane-bound core area. In all species, a microbody and mitochondrion are associated with the lipid globule. The number of mitochondria varies from 1 in some species to several or to over 30 in other species. In one isolate of R. pollinis-pini, there is 1 large mitochondrion and in the other there were 30–35 small mitochondria. The peripheral cytoplasm of all species contains clusters of vesicles or endoplasmic reticulum which bud from the double membrane system, vesicles of moderate electron density, and vacuoles of various sizes; R. capillaceum, R. patellarium, and R. subangulosum have in addition vesicles which contain very electron-dense material. Rhizophydium capillaceum and R. sphaerocarpum zoospores have virus-like particles and the R. biporosum zoospore contains a paracrystalline body. The taxonomic significance of the observations and the relationship of Rhizophydium to other chytrids are stressed in the Discussion.


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