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・ Acetone oxime
・ Acetone peroxide
・ Acetone thiosemicarbazone
・ Acetonedicarboxylic acid
・ AcetoneISO
・ Acetonema
・ Acetone–butanol–ethanol fermentation
・ Acetonide
・ Acetonitrile
・ Acetonitrile (data page)
・ Acetophenazine
・ Acetophenone
・ Acetophenone carboxylase
・ Acetorphine
・ Acetosa sagittata
Acetosyringone
・ Acetothermus
・ Acetoxolone
・ Acetoxy group
・ Acetoxyacetylaminofluorene
・ Acetoxybutynylbithiophene deacetylase
・ Acetoxycycloheximide
・ Acetoxyketobemidone
・ Acetrax
・ Acetrizoic acid
・ Acetropis gimmerthalii
・ Aceturic acid
・ Acetyl
・ Acetyl activating enzyme
・ Acetyl bromide


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Acetosyringone : ウィキペディア英語版
Acetosyringone

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Acetosyringone is a phenolic natural product, and is a chemical compound related to acetophenone and 2,6-dimethoxyphenol. It was first described in relation to lignan/phenylpropanoid-type phytochemicals, with isolation from a variety of plant sources, in particular, in relation to wounding and other physiologic changes.
Historically, this substance has been best known for its involvement in plant-pathogen recognition, especially its role as a signal attracting and transforming unique, oncogenic bacteria in genus ''Agrobacterium''. The ''virA'' gene on the Ti plasmid of ''Agrobacterium tumefaciens'' and the Ri plasmid of ''Agrobacterium rhizogenes'' is used by these soil bacteria to infect plants, via its encoding for a receptor for acetosyringone and other phenolic phytochemicals exuded by plant wounds. This compound also allows higher transformation efficiency in plants, in ''A. tumefaciens''-mediated transformation procedures, and so is of importance in plant biotechnology.
Acetosyringone can also be found in ''Posidonia oceanica'' and a wide variety of other plants. It is secreted at wounded site of dicotyledons. This compound enhances the ''Agrobacterium''-mediated gene transformation in dicot. Monocotyledons lack this wound response and it is considered as the limiting factor in ''Agrobacterium''-mediated gene transformation in monocots.
The compound is also produced by the male leaffooted bug (''Leptoglossus phyllopus'') and used in its communication system.〔(Acetosyringone on www.pherobase.com, the pheromones data base )〕
In vitro studies show that acetosyringone increases mycorrhizae formation in the fungus ''Glomus intraradices''.
Total synthesis of this simple natural product performed by Crawford et al. in 1956, but is of limited contemporary synthetic interest. A variety of acetosyringone analogs are available, including some which are covalent inactivators of cellular processes that involve acetosyringone.
== Chemical characteristics ==
Acetosyringone does not dissolve well in water. Although it has a melting point of about 125 degree Celsius, it is not wise to autoclave acetosyringone along with the medium used for (for example) plant infiltration by microbes.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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