scholarly journals Dark Protein Synthesis: Physiological Response to Nutrient Limitation of a Natural Phytoplankton Population

2001 ◽  
Vol 55 (1) ◽  
pp. 1-15
Author(s):  
S. (Satoru) Taguchi ◽  
Edward A. Laws
Weed Science ◽  
1983 ◽  
Vol 31 (6) ◽  
pp. 874-878 ◽  
Author(s):  
Emerson D. Nafziger ◽  
Fred W. Slife

Thirteen-day-old common cocklebur (Xanthium pensylvanicumWallr. # XANPE) plants were treated with 15 μg glyphosate [N-(phosphonomethyl)glycine] applied to the lowermost true leaves. Growth was inhibited rapidly following treatment. About 56% of applied14C-glyphosate was taken up within 8 h. Within 4 days after treatment, diffusive resistance increased in treated leaves but did not change in untreated leaves. Glyphosate had little effect on nonstructural carbohydrate content of leaves, but soluble carbohydrate levels of stems and roots had increased by 130 and 180%, respectively, by 56 h after treatment. The uptake of33P into roots was unaffected by the herbicide, but transport of P to the aerial tissues was severely inhibited. Effects such as inhibition of P movement could result from inhibition of protein synthesis.


1988 ◽  
Vol 10 (5) ◽  
pp. 941-955 ◽  
Author(s):  
Takeo Hama ◽  
Katsuji Matsunaga ◽  
Nobuhiko Handa ◽  
Mikio Takahashi

2021 ◽  
Author(s):  
Simon Diez ◽  
Molly Hydorn ◽  
Abigail Whalen ◽  
Jonathan Dworkin

Phenotypic heterogeneity of microbial populations can facilitate survival in dynamic environments by generating sub-populations of cells that may have differential fitness in a future environment. Bacillus subtilis cultures experiencing nutrient limitation contain distinct sub-populations of cells exhibiting either comparatively high or low protein synthesis activity. This heterogeneity requires the production of phosphorylated guanosine nucleotides (pp)ppGpp by three synthases: SasA, SasB, and RelA. Here we show that these enzymes differentially affect this bimodality: RelA and SasB are necessary to generate the sub-population of cells exhibiting low protein synthesis whereas SasA is necessary to generate cells exhibiting comparatively higher protein synthesis. The RelA product (pppGpp) allosterically activates SasB and we find, in contrast, that the SasA product (pGpp) competitively inhibits this activation. Finally, we provide in vivo evidence that this antagonistic interaction mediates the observed heterogeneity in protein synthesis. This work therefore identifies the mechanism underlying phenotypic heterogeneity in the central physiological process of protein synthesis.


2021 ◽  
Author(s):  
Vitul Agarwal ◽  
Chase C. James ◽  
Claire E. Widdicombe ◽  
Andrew D. Barton

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