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独脚金内酯信号传导化学调控的作用位点

Target sites for chemical regulation of strigolactone signaling.

作者信息

Nakamura Hidemitsu, Asami Tadao

机构信息

The Chemical Biology Laboratory, Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo Tokyo, Japan.

The Chemical Biology Laboratory, Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo Tokyo, Japan ; Program of Japan Science and Technology Agency, Core Research for Evolutional Science and Technology Kawaguchi, Japan ; King Abdulaziz University Jedda, Saudi Arabia.

出版信息

Front Plant Sci. 2014 Nov 5;5:623. doi: 10.3389/fpls.2014.00623. eCollection 2014.

Abstract

Demands for plant growth regulators (PGRs; chemicals that control plant growth) are increasing globally, especially in developing countries. Both positive and negative PGRs are widely used to enhance crop production and to suppress unwanted shoot growth, respectively. Strigolactones (SLs) are multifunctional molecules that function as phytohormones, inhibiting shoot branching and also functioning in the rhizospheric communication with symbiotic fungi and parasitic weeds. Therefore, it is anticipated that chemicals that regulate the functions of SLs will be widely used in agricultural applications. Although the SL biosynthetic pathway is not fully understood, it has been demonstrated that β-carotene isomerases, carotenoid cleavage dioxygenases (CCDs), and a cytochrome P450 monooxygenase are involved in strigolactone biosynthesis. A CCD inhibitor, abamine, which is also an inhibitor of abscisic acid biosynthesis, reduces the levels of SL in several plant species and reduces the germination rate of Orobanche minor seeds grown with tobacco. On the basis of the structure of abamine, several chemicals have been designed to specifically inhibit CCDs during SL synthesis. Cytochrome P450 monooxygenase is another target enzyme in the development of SL biosynthesis inhibitors, and the triazole-derived TIS series of chemicals is known to include SL biosynthesis inhibitors, although their target enzyme has not been identified. Recently, DWARF14 (D14) has been shown to be a receptor for SLs, and the D-ring moiety of SL is essential for its recognition by D14. A variety of SL agonists are currently under development and most agonists commonly contain the D-ring or a D-ring-like moiety. Several research groups have also resolved the crystal structure of D14 in the last two years. It is expected that this information on the D14 structure will be invaluable not only for developing SL agonists with novel structures but also in the design of inhibitors of SL receptors.

摘要

全球对植物生长调节剂(PGRs;控制植物生长的化学物质)的需求正在增加,尤其是在发展中国家。正、负植物生长调节剂分别被广泛用于提高作物产量和抑制不必要的枝条生长。独脚金内酯(SLs)是多功能分子,作为植物激素发挥作用,抑制枝条分枝,并在与共生真菌和寄生杂草的根际交流中发挥作用。因此,预计调节独脚金内酯功能的化学物质将在农业应用中广泛使用。尽管独脚金内酯的生物合成途径尚未完全了解,但已证明β-胡萝卜素异构酶、类胡萝卜素裂解双加氧酶(CCDs)和细胞色素P450单加氧酶参与独脚金内酯的生物合成。一种CCDs抑制剂阿巴美灵,它也是脱落酸生物合成的抑制剂,可降低几种植物物种中独脚金内酯的水平,并降低与烟草一起生长的小列当种子的发芽率。基于阿巴美灵的结构,已设计出几种化学物质以在独脚金内酯合成过程中特异性抑制CCDs。细胞色素P450单加氧酶是独脚金内酯生物合成抑制剂开发中的另一个靶标酶,尽管尚未确定其靶标酶,但已知三唑衍生的TIS系列化学物质包括独脚金内酯生物合成抑制剂。最近,DWARF14(D14)已被证明是独脚金内酯的受体,独脚金内酯的D环部分对于其被D14识别至关重要。目前正在开发多种独脚金内酯激动剂,大多数激动剂通常含有D环或类D环部分。在过去两年中,几个研究小组也解析了D14的晶体结构。预计这些关于D14结构的信息不仅对于开发具有新结构的独脚金内酯激动剂非常宝贵,而且在独脚金内酯受体抑制剂的设计中也具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be28/4220635/1c27dc4f7e42/fpls-05-00623-g001.jpg

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