Chemical and molecular genetic strategies to block ethylene perception for increased flower life

Ethylene has been known to cause many undesirable effects in a range of ornamental species. Blocking ethylene responses has been proved as an efficient strategy to enhance the longevity of the flowers. The most effective ways to conduct such interference are using chemical compounds or genetic manipulation. In the last 15 years a large number of volatile chemical compounds have been evaluated for their effects on ethylene production and perception. This has resulted in the discovery that cyclopropenes effectively block ethylene responses at the receptor level. The most promising among them are 1-methylcyclopropene (1-MCP) and a number of other substituted cyclopropenes. A lot of testing remains to be done to uncover the full potential of these compounds, but they do offer promising new ways to improve the postharvest quality and longevity of ornamentals. Another very effective way for controlling ethylene synthesis and perception is genetic modification. The most promising strategy seems to be the use of the mutant ethylene receptor gene, etr1-1, from Arabidopsis thaliana, especially when it is expressed under the control of a flower specific promoter

Ethylene supports colonization of plant roots by the mutualistic fungus Piriformospora indica

The mutualistic basidiomycete Piriformospora indica colonizes roots of mono- and dicotyledonous plants, and thereby improves plant health and yield. Given the capability of P. indica to colonize a broad range of hosts, it must be anticipated that the fungus has evolved efficient strategies to overcome plant immunity and to establish a proper environment for nutrient acquisition and reproduction. Global gene expression studies in barley identified various ethylene synthesis and signaling components that were differentially regulated in P. indica-colonized roots. Based on these findings we examined the impact of ethylene in the symbiotic association. The data presented here suggest that P. indica induces ethylene synthesis in barley and Arabidopsis roots during colonization. Moreover, impaired ethylene signaling resulted in reduced root colonization, Arabidopsis mutants exhibiting constitutive ethylene signaling, -synthesis or ethylene-related defense were hyper-susceptible to P. indica. Our data suggest that ethylene signaling is required for symbiotic root colonization by P. indica

Absorbance response of graphene oxide coated on tapered multimode optical fiber towards liquid ethanol

The investigation of graphene oxide (GO) for sensing applications is attractive due to its nanoscale structure and its sensing properties has yet to be fully understood. In this paper, optical response of GO coated optical fiber sensor towards ethanol is described. GO was coated onto a multimode tapered optical fiber by drop-casting technique. The coated fiber was exposed to 5–40% of ethanol in water. The films were characterized with field emission scanning electron microscope, ultraviolet-visible spectroscopy and Raman spectroscopy. The sensing is based on changes following the absorbance of the GO coated optical fiber upon exposure to ethanol. The developed sensor shows fast response and recovery with duration of 22 and 20 s, respectively. The sensor also displays high repeatability and reversibility

Phosphorylation Alters the Interaction of the Arabidopsis Phosphotransfer Protein AHP1 with Its Sensor Kinase ETR1

The ethylene receptor ethylene response 1 (ETR1) and the Arabidopsis histidine-containing phosphotransfer protein 1 (AHP1) form a tight complex in vitro. According to our current model ETR1 and AHP1 together with a response regulator form a phosphorelay system controlling the gene expression response to the plant hormone ethylene, similar to the two-component signaling in bacteria. The model implies that ETR1 functions as a sensor kinase and is autophosphorylated in the absence of ethylene. The phosphoryl group is then transferred onto a histidine at the canonical phosphorylation site in AHP1. For phosphoryl group transfer both binding partners need to form a tight complex. After ethylene binding the receptor is switched to the non-phosphorylated state. This switch is accompanied by a conformational change that decreases the affinity to the phosphorylated AHP1. To test this model we used fluorescence polarization and examined how the phosphorylation status of the proteins affects formation of the suggested ETR1−AHP1 signaling complex. We have employed various mutants of ETR1 and AHP1 mimicking permanent phosphorylation or preventing phosphorylation, respectively. Our results show that phosphorylation plays an important role in complex formation as affinity is dramatically reduced when the signaling partners are either both in their non-phosphorylated form or both in their phosphorylated form. On the other hand, affinity is greatly enhanced when either protein is in the phosphorylated state and the corresponding partner in its non-phosphorylated form. Our results indicate that interaction of ETR1 and AHP1 requires that ETR1 is a dimer, as in its functional state as receptor in planta