scholarly journals In vivo Antioxidative Activities in Natto Using Nematode Caenorhabditis elegans

2010 ◽  
Vol 57 (1) ◽  
pp. 12-19 ◽  
Author(s):  
Sachie Ibe ◽  
Tetsuya Hiroi ◽  
Kazunori Otobe
Keyword(s):  
Caenorhabditis Elegans ◽  
Nematode Caenorhabditis Elegans

scholarly journals Biological effects, translocation, and metabolism of quantum dots in the nematode Caenorhabditis elegans

2016 ◽  
Vol 5 (4) ◽  
pp. 1003-1011 ◽  
Author(s):  
Dayong Wang
Keyword(s):  
Quantum Dots ◽  
Caenorhabditis Elegans ◽  
Recent Progress ◽  
Biological Effects ◽  
Assay System ◽  
Nematode Caenorhabditis Elegans ◽  
C Elegans

We summarize recent progress on the biological effects, translocation, and metabolism of QDs in thein vivoassay system ofC. elegans.

Alterations in the pattern of gene expression following heat shock in the nematode Caenorhabditis elegans

1983 ◽  
Vol 61 (6) ◽  
pp. 480-487 ◽  
Author(s):  
Terry P. Snutch ◽  
David L. Baillie
Keyword(s):  
Caenorhabditis Elegans ◽  
Heat Shock ◽  
Elevated Temperatures ◽  
In Vitro Study ◽  
In Vitro Translation ◽  
Nematode Caenorhabditis Elegans ◽  
Stage Of Development ◽  
Heat Shock Responses

Exposure of the nematode Caenorhabditis elegans to elevated temperatures induces the preferential synthesis of eight major polypeptides of approximate molecular weights 81 000, 70 000, 41 000, 38 000, 29 000, 19 000, 18 000, and 16 000. In pulse-labelled worms these peptides first appear at 29 °C and continue to be synthesized up to lethal temperatures. They are heat inducible at every stage of development. While temperature elevation induces the synthesis of the heat-shock polypeptides, the in vivo synthesis of most other proteins present before heat shock is suppressed. In contrast, in vitro translation of mRNA from heat-shocked worms shows no alteration from the pattern of normal 20 °C mRNAs except for the appearance of the heat-shock mRNAs. An in vitro study of RNA from control and heat-shocked dauer larvae shows that this developmental variant possesses little translatable mRNA but, upon heat shock, synthesizes a set of messages corresponding to the heat-shock polypeptides. The low background of this system will be especially useful in the analysis and purification of heat-shock mRNA for molecular cloning experiments. Extensive similarities between the Drosophila and C. elegans heat-shock responses are shown, including homology between the 70-kdalton heat-shock genes of the two organisms.

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