Relevant bibliographies by topics / Iridoid synthase

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  2. Dissertations / Theses
  3. Books
  4. Conference papers

Academic literature on the topic 'Iridoid synthase'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Iridoid synthase"

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Aničić, Neda, and Danijela Mišić. "Unveiling the evolution of iridoid biosynthesis in the genus Nepeta: a mini review." Biologia Serbica 46, no. 1 (2024): 100–108. https://doi.org/10.5281/zenodo.13925848.

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<strong>Summary. </strong>The genus <em>Nepeta</em>, belonging to the Lamiaceae family, encompasses a diverse group of plants with significant biological activities attributed mainly to their iridoid compounds. This review provides a comprehensive analysis of recent research on iridoid biosynthesis, regulation, and evolutionary aspects within the <em>Nepeta</em> genus. The biological activities of <em>Nepeta</em> species, including repellent, phytotoxic, antimicrobial, and cytotoxic effects, have been extensively investigated, highlighting the potential applications of iridoids. Over the past
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Kries, Hajo, Franziska Kellner, Mohamed Omar Kamileen, and Sarah E. O'Connor. "Inverted stereocontrol of iridoid synthase in snapdragon." Journal of Biological Chemistry 292, no. 35 (2017): 14659–67. http://dx.doi.org/10.1074/jbc.m117.800979.

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Duan, Hongying, Wenxiao Liu, Yunpeng Zeng, Wenjing Jia, Huihui Wang, and Yanqing Zhou. "Expression analysis of key enzymes involved in the accumulation of iridoid in Rehmannia glutinosa." Plant Omics, no. 12(02):2019 (September 20, 2019): 102–8. http://dx.doi.org/10.21475/poj.12.02.19.p2221.

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As the traditional Chinese herb, Rehmannia glutinosa (R. glutinosa) has significant effects on health. The main active ingredient of R. glutinosa is iridoid. In this study, root, stem and leaf of R. glutinosa at five different growth stages were collected, the content of iridoid in R. glutinosa was determinated, and the expression of key enzymes in R. glutinosa was analyzed by quantitative real-time PCR (q-PCR). We found that the content of iridoid was increased continuously during the first three growth stages (I-III) of R. glutinosa. It reached the maximum value in root and leaf at growth st
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Kang, Ji-Nam, Jong-Won Han, So-Hee Yang, and Si-Myung Lee. "Co-Expression Analysis Reveals Differential Expression of Homologous Genes Associated with Specific Terpenoid Biosynthesis in Rehmannia glutinosa." Genes 13, no. 6 (2022): 1092. http://dx.doi.org/10.3390/genes13061092.

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Terpenoids are naturally occurring compounds involved in respiration, photosynthesis, membrane fluidity, and pathogen interactions and are classified according to the structure of their carbon skeleton. Although most terpenoids possess pharmacological activity, knowledge about terpenoid metabolism in medicinal plants is insufficient. Rehmannia glutinosa (R. glutinosa) is a traditional herb that is widely used in East Asia and has been reported to contain various terpenoids. In this study, we performed a comprehensive transcriptome analysis of terpenoid metabolism in R. glutinosa using two RNA
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Salim, Vonny, Brent Wiens, Sayaka Masada-Atsumi, Fang Yu, and Vincenzo De Luca. "7-Deoxyloganetic acid synthase catalyzes a key 3 step oxidation to form 7-deoxyloganetic acid in Catharanthus roseus iridoid biosynthesis." Phytochemistry 101 (May 31, 2014): 23–31. https://doi.org/10.1016/j.phytochem.2014.02.009.

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Salim, Vonny, Wiens, Brent, Masada-Atsumi, Sayaka, Yu, Fang, Luca, Vincenzo De (2014): 7-Deoxyloganetic acid synthase catalyzes a key 3 step oxidation to form 7-deoxyloganetic acid in Catharanthus roseus iridoid biosynthesis. Phytochemistry 101: 23-31, DOI: 10.1016/j.phytochem.2014.02.009, URL: http://dx.doi.org/10.1016/j.phytochem.2014.02.009
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Schmidt, Karin, Jan Petersen, Jennifer Munkert та ін. "PRISEs (progesterone 5β-reductase and/or iridoid synthase-like 1,4-enone reductases): Catalytic and substrate promiscuity allows for realization of multiple pathways in plant metabolism". Phytochemistry 156 (31 грудня 2018): 9–19. https://doi.org/10.1016/j.phytochem.2018.08.012.

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Schmidt, Karin, Petersen, Jan, Munkert, Jennifer, Egerer-Sieber, Claudia, Hornig, Michael, Muller, Yves A., Kreis, Wolfgang (2018): PRISEs (progesterone 5β-reductase and/or iridoid synthase-like 1,4-enone reductases): Catalytic and substrate promiscuity allows for realization of multiple pathways in plant metabolism. Phytochemistry 156: 9-19, DOI: 10.1016/j.phytochem.2018.08.012, URL: http://dx.doi.org/10.1016/j.phytochem.2018.08.012
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Sandholu, Anandsukeerthi, Jayati Sengupta, and Kiran Kulkarni. "Structural basis of iridoid synthase-mediated cyclization of 10-oxogeranial." Acta Crystallographica Section A Foundations and Advances 73, a2 (2017): C270. http://dx.doi.org/10.1107/s2053273317093032.

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Xiang, Beibei, Xiaoxue Li, Yan Wang, et al. "Cloning and Characterization of Two Iridoid Synthase Homologs from Swertia Mussotii." Molecules 22, no. 8 (2017): 1387. http://dx.doi.org/10.3390/molecules22081387.

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Munkert, Jennifer, Jacob Pollier, Karel Miettinen та ін. "Iridoid Synthase Activity Is Common among the Plant Progesterone 5β-Reductase Family". Molecular Plant 8, № 1 (2015): 136–52. http://dx.doi.org/10.1016/j.molp.2014.11.005.

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10

Klein, Jan, Elisa Horn, Mona Ernst та ін. "RNAi-mediated gene knockdown of progesterone 5β-reductases in Digitalis lanata reduces 5β-cardenolide content". Plant Cell Reports 40, № 9 (2021): 1631–46. http://dx.doi.org/10.1007/s00299-021-02707-3.

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Abstract Key message Studying RNAi-mediated DlP5βR1 and DlP5βR2 knockdown shoot culture lines of Digitalis lanata, we here provide direct evidence for the participation of PRISEs (progesterone 5β-reductase/iridoid synthase-like enzymes) in 5β-cardenolide formation. Abstract Progesterone 5β-reductases (P5βR) are assumed to catalyze the reduction of progesterone to 5β-pregnane-3,20-dione, which is a crucial step in the biosynthesis of the 5β-cardenolides. P5βRs are encoded by VEP1-like genes occurring ubiquitously in embryophytes. P5βRs are substrate-promiscuous enone-1,4-reductases recently ter
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Dissertations / Theses on the topic "Iridoid synthase"

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Petersen, Jan-Henrik [Verfasser], Wolfgang [Akademischer Betreuer] Kreis та Wolfgang [Gutachter] Kreis. "Optimierung der Substratumsetzung von PRISE: Progesteron-5β-Reduktasen/Iridoid-Synthasen / Jan-Henrik Petersen ; Gutachter: Wolfgang Kreis ; Betreuer: Wolfgang Kreis". Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2018. http://d-nb.info/1163455830/34.

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Serre, Nathalie. "Contribution à l'étude de la chimie de trois iridoi͏̈des : l'aucuboside, le catalposide et le monomélittoside." Paris 5, 1999. http://www.theses.fr/1999PA05P124.

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Li, Jihui. "Copper-Catalyzed Domino C-N Bond Formation for Synthesis of N-Containing Compounds (Benzimidazoles, Imidazoles, and Guanidines) - Approach toward Total Synthesis of Natural Product Raputindoles." Thesis, Paris 11, 2013. http://www.theses.fr/2013PA112130.

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Cette thèse est constituée de trois parties : 1) Le contexte bibliographique, 2) le développement de réactions domino cupro-catalysées et 3) une approche vers la synthèse totale des raputindoles.La première partie introduit d’abord le concept de réactions domino ainsi que leurs applications, puis les réactions catalysées par du cuivre permettant de former des liaisons C-N sont passées en revue en incluant les couplages de Ullmann, Goldberg et de Chan-Lam, les séquences d’activation oxydante de liaisons C-H/formation de liaison C-N, l’insertion de nitrènes et l’hydroamination de liaisons C-C mu
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Books on the topic "Iridoid synthase"

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Kaiser, Anja Sabine. Asymmetrische Synthese von Ramulosin und iridoiden Naturstoffen durch Michael-Addition via SAMP-, RAMP-Hydrazone. 1997.

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Conference papers on the topic "Iridoid synthase"

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Dorfner, M., J. Klein, H. Lanig, W. Kreis та J. Munkert. "Identifying structural features for changing substrate preferences in two Plantago PRISEs (progesterone 5β-reductase and /or iridoid synthase)". У GA – 69th Annual Meeting 2021, Virtual conference. Georg Thieme Verlag, 2021. http://dx.doi.org/10.1055/s-0041-1736952.

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