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Bioscience, Biotechnology, and Biochemistry Volume 82, 2018 - Issue 8
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Chemical regulators of plant hormones and their applications in basic research and agricultureFootnote*

Kai JiangGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, JapanORCID Iconhttp://orcid.org/0000-0001-9901-5293
ORCID Icon &
Tadao AsamiGraduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, JapanCorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0003-0774-6203
ORCID Icon
Pages 1265-1300 | Received 09 Nov 2017, Accepted 30 Mar 2018, Published online: 20 Apr 2018

Figures & data

Figure 1. Chemical structures of auxin-related chemicals and simplified schematic model of auxin biosynthesis, transport, and signal transduction. A detailed description of these processes is described in the section on auxin. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 1. Chemical structures of auxin-related chemicals and simplified schematic model of auxin biosynthesis, transport, and signal transduction. A detailed description of these processes is described in the section on auxin. The numbers in bold correspond with the numbers in Figure 1(A) and they are unique call numbers in this paper.

Figure 2. Chemical structures of gibberellin-related chemicals and simplified schematic model of gibberellin biosynthesis, catabolism, transport, and signal transduction. A detailed description of these processes is described in the section on gibberellins. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 2. Chemical structures of gibberellin-related chemicals and simplified schematic model of gibberellin biosynthesis, catabolism, transport, and signal transduction. A detailed description of these processes is described in the section on gibberellins. The numbers in bold correspond with the numbers in Figure 2(A) and they are unique call numbers in this paper.

Figure 3. Chemical structures of cytokinin-related chemicals and simplified schematic model of cytokinin biosynthesis, transport, and signal transduction. A detailed description of these processes is described in the section on cytokinins. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 3. Chemical structures of cytokinin-related chemicals and simplified schematic model of cytokinin biosynthesis, transport, and signal transduction. A detailed description of these processes is described in the section on cytokinins. The numbers in bold correspond with the numbers in Figure 3(A) and they are unique call numbers in this paper.

Figure 4. Chemical structures of abscisic acid-related chemicals and simplified schematic model of abscisic acid biosynthesis, catabolism, transport, and signal transduction. A detailed description of these processes is described in the section on abscisic acid. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 4. Chemical structures of abscisic acid-related chemicals and simplified schematic model of abscisic acid biosynthesis, catabolism, transport, and signal transduction. A detailed description of these processes is described in the section on abscisic acid. The numbers in bold correspond with the numbers in Figure 4(A) and they are unique call numbers in this paper.

Figure 5. Chemical structures of ethylene-related chemicals and simplified schematic model of ethylene biosynthesis and signal transduction. A detailed description of the processes is described in the section on ethylene. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 5. Chemical structures of ethylene-related chemicals and simplified schematic model of ethylene biosynthesis and signal transduction. A detailed description of the processes is described in the section on ethylene. The numbers in bold correspond with the numbers in Figure 5(A) and they are unique call numbers in this paper.

Figure 6. Chemical structures of brassinosteroid-related chemicals and simplified schematic model of brassinosteroid biosynthesis and signal transduction. A detailed description of the processes is described in the section on brassinosteroids. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 6. Chemical structures of brassinosteroid-related chemicals and simplified schematic model of brassinosteroid biosynthesis and signal transduction. A detailed description of the processes is described in the section on brassinosteroids. The numbers in bold correspond with the numbers in Figure 6(A) and they are unique call numbers in this paper.

Figure 7. Chemical structures of jasmonic acid-related chemicals and simplified schematic model of jasmonic acid biosynthesis and signal transduction. A detailed description of the processes is described in the section on jasmonic acid. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 7. Chemical structures of jasmonic acid-related chemicals and simplified schematic model of jasmonic acid biosynthesis and signal transduction. A detailed description of the processes is described in the section on jasmonic acid. The numbers in bold correspond with the numbers in Figure 7(A) and they are unique call numbers in this paper.

Figure 8. Chemical structures of salicylic acid-related chemicals and simplified schematic model of salicylic acid biosynthesis, catabolism, transport, and signal transduction. A detailed description of these processes is described in the section on salicylic acid. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this manuscript.

Figure 8. Chemical structures of salicylic acid-related chemicals and simplified schematic model of salicylic acid biosynthesis, catabolism, transport, and signal transduction. A detailed description of these processes is described in the section on salicylic acid. The numbers in bold correspond with the numbers in Figure 8(A) and they are unique call numbers in this manuscript.

Figure 9. Chemical structures of strigolactone-related chemicals and simplified schematic model of strigolactone biosynthesis and signal transduction. A detailed description of the processes is described in the section on strigolactone. The numbers in bold correspond with the numbers in (A) and they are unique call numbers in this paper.

Figure 9. Chemical structures of strigolactone-related chemicals and simplified schematic model of strigolactone biosynthesis and signal transduction. A detailed description of the processes is described in the section on strigolactone. The numbers in bold correspond with the numbers in Figure 9(A) and they are unique call numbers in this paper.

Figure 10. Schematic representation of the workflow of chemical screening (adapted from Dejonghe and Russinova396)) and its applicable fields.

Figure 10. Schematic representation of the workflow of chemical screening (adapted from Dejonghe and Russinova396)) and its applicable fields.

Table 1. Chemicals and their call numbers in this manuscript.

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A New Non-Azole Inhibitor of ABA 8′-Hydroxylase: Effect of the Hydroxyl Group Substituted for Geminal Methyl Groups in the Six-Membered Ring.
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Regulation of Strigolactone Biosynthesis by Gibberellin Signaling.
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Syntheses of Jasmonic Acid Related Compounds and Their Structure-Activity Relationships on the Growth of Rice Seedings
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A new lead compound for abscisic acid biosynthesis inhibitors targeting 9-cis-epoxycarotenoid dioxygenase
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25-Methyldolichosterone, a new brassinosteroid with a tertiary butyl group from immature seed of Phaseolus vulgaris
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A century of gibberellin research
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Effects of strigolactone-biosynthesis inhibitor TIS108 on Arabidopsis
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Gibberellin-like Activity of Helminthosporol and Helminthosporic Acid
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Triplin, a small molecule, reveals copper ion transport in ethylene signaling from ATX1 to RAN1.
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COI1: An Arabidopsis Gene Required for Jasmonate-Regulated Defense and Fertility
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非ステロイド型ブラシノライド様化合物NSBR1の発見
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Structural modifications of strigol analogs. Influence of the B and C rings on the bioactivity of the germination stimulant GR24
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Regulators of cell division in plant tissues—II. A cytokinin in plant extracts: Isolation and interaction with other growth regulators☆
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Smoke and Hormone Mirrors: Action and Evolution of Karrikin and Strigolactone Signaling
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Aspirin prevents wound-induced gene expression in tomato leaves by blocking jasmonic acid biosynthesis
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Multidrug Resistance-like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development
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Methods and Protocols
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Arabidopsis CYP94B3 Encodes Jasmonyl-l-Isoleucine 12-Hydroxylase, a Key Enzyme in the Oxidative Catabolism of Jasmonate
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Screening and characterization of an inhibitory chemical specific to Arabidopsis gibberellin 2-oxidases.
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