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. 2022 Nov 29;13:1008993. doi: 10.3389/fpls.2022.1008993

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Copyright © 2022 Maheshwari, Garg, Hasan, V, Meena, Singh and Tyagi

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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(A)Terpenoid pathway. Paclobutrazol inhibition is indicated by . (CPS), Copalyl diphosphate synthase; (KAO), ent-kaurenoic acid oxidase; (KS), ent-kaurene synthase; (GGPPS), geranylgeranyl pyrophosphate synthase; (PSY), phytoene synthase; (ZEP), zeaxanthin epoxidase; (NCED), 9-cisepoxycarotenoid dioxygenase; (CHS), chlorophyll Synthase; (GGRS), geranylgeranyl reductase. (B) Chemical structure of some triazoles.

Inline graphic — (A)Terpenoid pathway. Paclobutrazol inhibition is indicated by . (CPS), Copalyl diphosphate synthase; (KAO), ent-kaurenoic acid oxidase; (KS), ent-kaurene synthase; (GGPPS), geranylgeranyl pyrophosphate synthase; (PSY), phytoene synthase; (ZEP), zeaxanthin epoxidase; (NCED), 9-cisepoxycarotenoid dioxygenase; (CHS), chlorophyll Synthase; (GGRS), geranylgeranyl reductase. (B) Chemical structure of some triazoles.