Enzymatic adaptations for the biosynthesis of ethyl-substituted juvenile hormones
乙基取代保幼激素生物合成的酶促适应
基本信息
- 批准号:171350-2007
- 负责人:
- 金额:$ 1.38万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2011
- 资助国家:加拿大
- 起止时间:2011-01-01 至 2012-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The disruption of hormone functions has long been viewed as a promising avenue for the development of insect-specific, environmentally friendly pest control products. One such hormone, "juvenile hormone" (JH), plays critical roles in insect development and reproduction. Inhibition of its biosynthesis during larval development can trigger the premature - and typically fatal - transformation into the adult form (i.e., metamorphosis), while a similar inhibition in adults can suppress reproduction. JH is a terpenoid compound whose biosynthesis involves some late-step, insect-specific enzymes as well as several other enzymes that, in other organisms, are involved in the production of common metabolites such as cholesterol. Among the latter group of enzymes, we identified one that displays features apparently unique to a group of insects known as the Lepidoptera (caterpillars, moths, butterflies). This lepidopteran enzyme, farnesyl diphosphate synthase (FPPS), displays selectivity for ethyl-substituted substrates, which are the precursors of the unusual JHs molecules found in these insects; the lepidopeteran JHs differ from those observed in other taxa in that their carbon skeletons bear ethyl branches rarely seen in related compounds of this family. The proposed research focuses on the characterization of the lepidopteran version of this enzyme, including (i) the identification of its active form, (ii) the study of its precise roles in JH biosynthesis and other metabolic pathways, and (iii) the identification of the structural features that confer selectivity for homologous substrates. The knowledge generated through this research is expected to pave the way to the rational design of FPPS inhibitors that specifically target the Lepidoptera; such compounds could form the basis of novel, target-specific pest control products.
长期以来,激素功能的破坏一直被视为开发昆虫特异性、环境友好型害虫控制产品的有希望的途径。保幼激素(juvenile hormone,JH)在昆虫的发育和繁殖中起着重要作用。在幼虫发育过程中抑制其生物合成可引发过早-并且通常是致命的-转化为成虫形式(即,变态),而在成年人中类似的抑制可以抑制繁殖。JH是一种萜类化合物,其生物合成涉及一些后期步骤,昆虫特异性酶以及其他几种酶,在其他生物体中,这些酶参与产生常见的代谢物,如胆固醇。在后一组酶中,我们确定了一种酶,它显示出一组被称为鳞翅目(毛虫,飞蛾,蝴蝶)的昆虫所特有的特征。这种鳞翅目酶,法呢基二磷酸合酶(FPPS),显示选择性乙基取代的底物,这是不寻常的JHS分子在这些昆虫中发现的前体;鳞翅目JHS不同于其他类群中观察到的,他们的碳骨架带有乙基分支很少看到这个家庭的相关化合物。拟议的研究重点是这种酶的鳞翅目版本的表征,包括(i)其活性形式的鉴定,(ii)其在JH生物合成和其他代谢途径中的确切作用的研究,以及(iii)赋予同源底物的选择性的结构特征的鉴定。通过这项研究产生的知识,预计将铺平道路的FPPS抑制剂,专门针对鳞翅目昆虫的合理设计,这些化合物可以形成新的,目标特定的害虫控制产品的基础。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Cusson, Michel其他文献
Genomic and morphological features of a banchine polydnavirus: Comparison with bracoviruses and ichnoviruses
- DOI:
10.1128/jvi.02702-06 - 发表时间:
2007-06-01 - 期刊:
- 影响因子:5.4
- 作者:
Lapointe, Renee;Tanaka, Kohjiro;Cusson, Michel - 通讯作者:
Cusson, Michel
The molecular biology toolbox and its use in basic and applied insect science
- DOI:
10.1641/b580806 - 发表时间:
2008-09-01 - 期刊:
- 影响因子:10.1
- 作者:
Cusson, Michel - 通讯作者:
Cusson, Michel
Ultrastructural and genomic characterization of a second banchine polydnavirus confirms the existence of shared features within this ichnovirus lineage
- DOI:
10.1099/vir.0.052506-0 - 发表时间:
2013-08-01 - 期刊:
- 影响因子:3.8
- 作者:
Djoumad, Abdelmadjid;Stoltz, Don;Cusson, Michel - 通讯作者:
Cusson, Michel
Characterization and tissue-specific expression of two lepidopteran farnesyl diphosphate synthase homologs:: Implications for the biosynthesis of ethyl-substituted juvenile hormones
- DOI:
10.1002/prot.21057 - 发表时间:
2006-11-15 - 期刊:
- 影响因子:2.9
- 作者:
Cusson, Michel;Beliveau, Catherine;Grant, Guy H. - 通讯作者:
Grant, Guy H.
Prophenoloxidases 1 and 2 from the spruce budworm, Choristoneura fumiferana:: Molecular cloning and assessment of transcriptional regulation by a polydnavirus
- DOI:
10.1002/arch.20227 - 发表时间:
2008-04-01 - 期刊:
- 影响因子:2.2
- 作者:
Doucet, Daniel;Beliveau, Catherine;Cusson, Michel - 通讯作者:
Cusson, Michel
Cusson, Michel的其他文献
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{{ truncateString('Cusson, Michel', 18)}}的其他基金
Functional and structural characterization of an insect mevalonate pathway enzyme
昆虫甲羟戊酸途径酶的功能和结构表征
- 批准号:
RGPIN-2019-04795 - 财政年份:2022
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Functional and structural characterization of an insect mevalonate pathway enzyme
昆虫甲羟戊酸途径酶的功能和结构表征
- 批准号:
RGPIN-2019-04795 - 财政年份:2021
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Functional and structural characterization of an insect mevalonate pathway enzyme
昆虫甲羟戊酸途径酶的功能和结构表征
- 批准号:
RGPIN-2019-04795 - 财政年份:2020
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Functional and structural characterization of an insect mevalonate pathway enzyme
昆虫甲羟戊酸途径酶的功能和结构表征
- 批准号:
RGPIN-2019-04795 - 财政年份:2019
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Properties and functions of farnesyl diphosphate synthase paralogs in the Lepidoptera
鳞翅目法尼基二磷酸合酶旁系同源物的特性和功能
- 批准号:
171350-2012 - 财政年份:2016
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Properties and functions of farnesyl diphosphate synthase paralogs in the Lepidoptera
鳞翅目法尼基二磷酸合酶旁系同源物的特性和功能
- 批准号:
171350-2012 - 财政年份:2015
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Properties and functions of farnesyl diphosphate synthase paralogs in the Lepidoptera
鳞翅目法尼基二磷酸合酶旁系同源物的特性和功能
- 批准号:
171350-2012 - 财政年份:2014
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Properties and functions of farnesyl diphosphate synthase paralogs in the Lepidoptera
鳞翅目法尼基二磷酸合酶旁系同源物的特性和功能
- 批准号:
171350-2012 - 财政年份:2013
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Properties and functions of farnesyl diphosphate synthase paralogs in the Lepidoptera
鳞翅目法尼基二磷酸合酶旁系同源物的特性和功能
- 批准号:
171350-2012 - 财政年份:2012
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
Enzymatic adaptations for the biosynthesis of ethyl-substituted juvenile hormones
乙基取代保幼激素生物合成的酶促适应
- 批准号:
171350-2007 - 财政年份:2010
- 资助金额:
$ 1.38万 - 项目类别:
Discovery Grants Program - Individual
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