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Journal articles on the topic 'Plant chemotaxonomy'

Author: Grafiati

Published: 4 June 2021

Last updated: 23 February 2023

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1

Citoglu, G. S., B. S. Yilmaz, B. Tarikahya, and R. Tipirdamaz. "Chemotaxonomy of Ballota Species." Chemistry of Natural Compounds 41, no. 3 (2005): 299–302. http://dx.doi.org/10.1007/s10600-005-0134-7.

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2

Asanova, Gulzina, Alexandra Dodonova, and Wojciech Push. "Identification of chemotaxonomic plant markers from the genus Centaurea L." Bulletin of the Karaganda University. “Biology, medicine, geography Series” 99, no. 3 (2020): 21–28. http://dx.doi.org/10.31489/2020bmg3/21-28.

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The use of chemotaxonomic methods for studying plants allows you to help identify the ancestral and species affiliation of closely related plants. Chemotaxonomy is especially useful for systematically young groups of plant taxa, characterized by great variability in morphological features, difficulty in identifying and clarifying systematic affiliation. The article analyses the content of various groups of biologically active compounds in plants of the genus Centaurea L. to find the most convenient chemotaxonomic markers. As a result of the analysis of the variability of flavonoids, sesquiterp

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3

Cohen, Zvi, Maria Cristina Margheri, and Luisa Tomaselli. "Chemotaxonomy of cyanobacteria." Phytochemistry 40, no. 4 (1995): 1155–58. http://dx.doi.org/10.1016/0031-9422(95)00335-5.

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4

Manhart, James R. "Chemotaxonomy of the genus Carex (Cyperaceae)." Canadian Journal of Botany 68, no. 7 (1990): 1457–61. http://dx.doi.org/10.1139/b90-184.

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The major categories of chemosystematic comparisons that were used successfully or are of potential use in Carex include flavonoid analysis, enzyme electrophoresis, and chloroplast DNA mapping and sequencing. The flavonoid work consists mostly of broad scale comparisons of aglycone distributions in a number of sedge genera to include some members of Carex. These comparisons proved to be of limited use in understanding phylogenetic relationships within the genus Carex. However, detailed flavonoid analyses of sections Laxiflorae and Acrocystis demonstrated the utility of flavonoid surveys in Car

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5

Yeo, Peter F., and Helen Widler-Kiefer. "The chemotaxonomy ofGeranium (Geraniaceae)." Plant Systematics and Evolution 173, no. 1-2 (1990): 1–15. http://dx.doi.org/10.1007/bf00937759.

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6

Reddy, M. Satyanarayana, K. Kiran Mai, M. Radhakrishnaiah, and L. L. Narayana. "Chemotaxonomy of Viticeae (Verbenaceae)." Feddes Repertorium 101, no. 3-4 (1990): 153–57. http://dx.doi.org/10.1002/fedr.4911010307.

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7

Reddy, M. Satyanarayana, K. Kiran Mai, M. Radhakrishnaiah, and L. L. Narayana. "Chemotaxonomy of Viticeae (Verbenaceae)." Feddes Repertorium 101, no. 3-4 (2008): 153–57. http://dx.doi.org/10.1002/fedr.19901010307.

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8

Sofrenić, Ivana, Boban Anđelković, Dejan Gođevac, et al. "Metabolomics as a Potential Chemotaxonomical Tool: Application on the Selected Euphorbia Species Growing Wild in Serbia." Plants 12, no. 2 (2023): 262. http://dx.doi.org/10.3390/plants12020262.

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Chemotaxonomy presents various challenges that need to be overcome in order to obtain valid and reliable results. Individual genetic and environmental variations can give a false picture and lead to wrong conclusions. Applying a holistic approach, based on multivariate data analysis, these challenges can be overcome. Thus, a metabolomics approach has to be optimized depending on the subject of research. We used 1H NMR-based metabolomics as a potential chemotaxonomic tool on the selected Euphorbia species growing wild in Serbia. Principal components analysis (PCA), soft independent modeling by

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9

Guiso, Marcella, Grazia Tassone, Marcello Nicoletti, Mauro Serafini, and Armandodoriano Bianco. "Chemotaxonomy of iridoids inLinaria vulgaris." Natural Product Research 21, no. 13 (2007): 1212–16. http://dx.doi.org/10.1080/14786410701536403.

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10

Nageshwar, G., M. Radhakrishnaiah, and L. L. Narayana. "Numerical chemotaxonomy of Amherstieae (Caesalpinioideae)." Feddes Repertorium 97, no. 5-6 (1986): 285–89. http://dx.doi.org/10.1002/fedr.4910970509.

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11

Anuradha, S. M. J., M. Radhakrishnaiah, and L. L. Narayana. "Numerical chemotaxonomy of some Mimosaceae." Feddes Repertorium 98, no. 3-4 (1987): 247–52. http://dx.doi.org/10.1002/fedr.4910980307.

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12

Satyavathi, S., M. Radhakrishnaiah, and L. L. Narayana. "Numerical chemotaxonomy of some Bignoniaceae." Feddes Repertorium 98, no. 7-8 (1987): 391–97. http://dx.doi.org/10.1002/fedr.4910980706.

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13

Rao, S. R. Shanmukha, and M. Leela. "Chemotaxonomy of someIpomoea L. (Convolvulaceae)." Feddes Repertorium 103, no. 5-6 (1992): 351–55. http://dx.doi.org/10.1002/fedr.4921030510.

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14

Satyavathi, S., M. Radhakrishnaiah, and L. L. Narayana. "Numerical chemotaxonomy of some Bignoniaceae." Feddes Repertorium 98, no. 7-8 (2008): 391–97. http://dx.doi.org/10.1002/fedr.19870980706.

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15

Oni, Feyisara Eyiwumi, Qassim Esmaeel, Joseph Tobias Onyeka, et al. "Pseudomonas Lipopeptide-Mediated Biocontrol: Chemotaxonomy and Biological Activity." Molecules 27, no. 2 (2022): 372. http://dx.doi.org/10.3390/molecules27020372.

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Pseudomonas lipopeptides (Ps-LPs) play crucial roles in bacterial physiology, host–microbe interactions and plant disease control. Beneficial LP producers have mainly been isolated from the rhizosphere, phyllosphere and from bulk soils. Despite their wide geographic distribution and host range, emerging evidence suggests that LP-producing pseudomonads and their corresponding molecules display tight specificity and follow a phylogenetic distribution. About a decade ago, biocontrol LPs were mainly reported from the P. fluorescens group, but this has drastically advanced due to increased LP diver

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16

Zidorn, Christian. "Plant chemophenetics − A new term for plant chemosystematics/plant chemotaxonomy in the macro-molecular era." Phytochemistry 163 (July 2019): 147–48. http://dx.doi.org/10.1016/j.phytochem.2019.02.013.

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17

Mottaghipisheh, Javad. "Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities." Plants 10, no. 8 (2021): 1577. http://dx.doi.org/10.3390/plants10081577.

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The present review comprehensively gathered phytochemical, bioactivity, and pharmacokinetic reports on a linear furanocoumarin, namely oxypeucedanin. Oxypeucedanin (OP), which structurally contains an epoxide ring, has been majorly isolated from ethyl acetate-soluble partitions of several genera, particularly Angelica, Ferulago, and Prangos of the Apiaceae family; and Citrus, belonging to the Rutaceae family. The methanolic extract of Angelica dahurica roots has been analytically characterized as the richest natural OP source. This naturally occurring secondary metabolite has been described to

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18

R�nsted, N., H. Franzyk, P. M�lgaard, J. W. Jaroszewski, and S. R. Jensen. "Chemotaxonomy and evolution of Plantago L." Plant Systematics and Evolution 242, no. 1-4 (2003): 63–82. http://dx.doi.org/10.1007/s00606-003-0057-3.

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19

Rao, S. R. Shanmukha, and M. Leela. "Chemotaxonomy of some Ipomoea L. (Convolvulaceae)." Feddes Repertorium 103, no. 5-6 (2008): 351–55. http://dx.doi.org/10.1002/fedr.19921030510.

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20

Vitikainen, Orvo. "William Nylander (1822–1899) and Lichen Chemotaxonomy." Bryologist 104, no. 2 (2001): 263–67. http://dx.doi.org/10.1639/0007-2745(2001)104[0263:wnalc]2.0.co;2.

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21

Kharazian, Navaz, and Mohammad Reza Rahimineja. "Chemotaxonomy of Wild Diploid Triticum L. (Poaceae) Species in Iran." International Journal of Botany 4, no. 3 (2008): 260–68. http://dx.doi.org/10.3923/ijb.2008.260.268.

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22

Mohamed, E. Zain, H. Bahkali Ali, and R. Al Othman Monerah. "Developments in using fatty acids in fungal chemotaxonomy." African Journal of Microbiology Research 7, no. 38 (2013): 4638–45. http://dx.doi.org/10.5897/ajmr12.090.

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23

Dunstan, Graeme A., Malcolm R. Brown, and John K. Volkman. "Cryptophyceae and rhodophyceae; chemotaxonomy, phylogeny, and application." Phytochemistry 66, no. 21 (2005): 2557–70. http://dx.doi.org/10.1016/j.phytochem.2005.08.015.

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24

Kodama, Taketoshi, Yukiko Taniuchi, Hiromi Kasai, Tamaha Yamaguchi, Misato Nakae, and Yutaka Okumura. "Empirical estimation of marine phytoplankton assemblages in coastal and offshore areas using an in situ multi-wavelength excitation fluorometer." PLOS ONE 17, no. 2 (2022): e0257258. http://dx.doi.org/10.1371/journal.pone.0257258.

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Phytoplankton assemblages are essential for understanding the quality of primary production in marine ecosystems. Here, we describe the development of a methodology for monitoring marine phytoplankton assemblages using an in situ multi-wavelength excitation fluorometer (MEX). The MEX recorded the fluorescence excited with nine light-emitting diodes, temperature, and sensor depth. We prepared reference datasets comprising MEX fluorescence and plant pigment-based phytoplankton assemblages of nine chemotaxonomy groups (diatoms, dinoflagellates, cryptophytes, chlorophytes, haptophytes type 3, hapt

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25

Spring, Otmar, Volker Klemt, Klaus Albert, and Achim Hager. "A Furanoheliangolide in Helianthus debilis; Implications for a Chemotaxonomy of the Genus Helianthus." Zeitschrift für Naturforschung C 41, no. 7-8 (1986): 695–98. http://dx.doi.org/10.1515/znc-1986-7-806.

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Abstract Leaves from Helianthus debilis subsp. cucumerifolius yielded the furanoheliangolide 17,18-dihydrobudlein A . The same compound has been previously isolated from Viguiera hemsleyana, V. procumbens and Helianthus strumosus. 17,18-dihydrobudlein A revealed strong antimicrobial, insecticidal and plant growth inhibiting activity. Its distribution within the plant is restricted to the leaves. Implications for the chemotaxonomy of the genus Helianthus are discussed.

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26

Prebble, John N. "Jeffrey Barry Harborne. 1 September 1928 — 21 July 2002." Biographical Memoirs of Fellows of the Royal Society 56 (January 2010): 131–47. http://dx.doi.org/10.1098/rsbm.2010.0012.

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Jeffrey Harborne made a major contribution to the discipline of phytochemistry. Originally an organic chemist, he became an academic leader in the biochemistry of secondary metabolites, particularly flavonoids and also other plant phenols. He contributed significantly to areas at the interface between chemistry and traditional areas of plant science, systematics and ecology. His early research was influential on the rise in importance of both plant chemotaxonomy and biochemical ecology.

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27

Stadler, Marc, Yu-Ming Ju, and Jack D. Rogers. "Chemotaxonomy of Entonaema, Rhopalostroma and other Xylariaceae." Mycological Research 108, no. 3 (2004): 239–56. http://dx.doi.org/10.1017/s0953756204009347.

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28

Stadler, Marc, Hartmund Wollweber, Andrea Mühlbauer, et al. "Molecular chemotaxonomy of Daldinia and other Xylariaceae." Mycological Research 105, no. 10 (2001): 1191–205. http://dx.doi.org/10.1016/s0953-7562(08)61990-5.

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29

Lund, Flemming, and Jens C. Frisvad. "Chemotaxonomy of Penicillium aurantiogriseum and related species." Mycological Research 98, no. 5 (1994): 481–92. http://dx.doi.org/10.1016/s0953-7562(09)80466-8.

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30

Hegnauer, R. "Phytochemistry and plant taxonomy — an essay on the chemotaxonomy of higher plants." Phytochemistry 25, no. 7 (1986): 1519–35. http://dx.doi.org/10.1016/s0031-9422(00)81204-2.

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31

Barberio, John, and John Twibell. "Chemotaxonomy of plant species using headspace sampling, thermal desorption and capillary GC." Journal of High Resolution Chromatography 14, no. 9 (1991): 637–39. http://dx.doi.org/10.1002/jhrc.1240140919.

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32

Frisvad, Jens C., and Ole Filtenborg. "Terverticillate Penicillia: Chemotaxonomy and Mycotoxin Production." Mycologia 81, no. 6 (1989): 837. http://dx.doi.org/10.2307/3760103.

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33

Frisvad, Jens C., and Ole Filtenborg. "Terverticillate Penicillia: Chemotaxonomy and Mycotoxin Production." Mycologia 81, no. 6 (1989): 837–61. http://dx.doi.org/10.1080/00275514.1989.12025674.

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34

Holden, Antony N. G., and Paul G. Mahlberg. "Application of chemotaxonomy of leafy spurges (Euphorbia spp.) in biological control." Canadian Journal of Botany 70, no. 8 (1992): 1529–36. http://dx.doi.org/10.1139/b92-192.

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Triterpenoid profiles from latex of 56 accessions of European leafy spurges (Euphorbia spp.) were analyzed by gas–liquid chromatography. Qualitative and quantitative differences for components of the profiles were employed to distinguish between accessions. Triterpenoid profiles were diagnostic for the species, E. amygdaloides, E. agraria, E. cyparissias, E. lucida, and E. seguierana and were similar for each of these species in accessions collected from distant areas of Europe. By contrast, the 37 accessions of the E. esula complex were separated into 15 groups on qualitative and quantitative

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35

Stadler, Marc, Hans-Volker Tichy, Eleni Katsiou, and Veronika Hellwig. "Chemotaxonomy of Pochonia and other conidial fungi with Verticillium-like anamorphs." Mycological Progress 2, no. 2 (2003): 95–122. http://dx.doi.org/10.1007/s11557-006-0048-1.

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36

Jensen, Søren Rosendal. "A re‐examination of Sanango racemosum. 3. Chemotaxonomy." TAXON 43, no. 4 (1994): 619–23. http://dx.doi.org/10.2307/1223547.

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37

Folkestad, Kirsten, Klaus Høiland, Berit Smestad Paulsen, and Karl Egil Malterud. "Alkaloid chemotaxonomy of Nordic Papaver sect. Scapiflora (Papaveraceae)." Nordic Journal of Botany 8, no. 2 (1988): 139–46. http://dx.doi.org/10.1111/j.1756-1051.1988.tb00493.x.

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38

Jensen, Henrik Fischer W., Søren Rosendal Jensen, and Bent Juhl Nielsen. "Chemotaxonomy of the acanthaceae. Iridoids and quaternary amines." Phytochemistry 27, no. 8 (1988): 2581–89. http://dx.doi.org/10.1016/0031-9422(88)87029-8.

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39

Frezza, Venditti, Toniolo, et al. "Pedicularis L. Genus: Systematics, Botany, Phytochemistry, Chemotaxonomy, Ethnopharmacology, and Other." Plants 8, no. 9 (2019): 306. http://dx.doi.org/10.3390/plants8090306.

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In this review, the relevance of the plant species belonging to the Pedicularis L. genus has been considered from different points of view. Particular emphasis was given to phytochemistry and ethnopharmacology, since several classes of natural compounds have been reported within this genus and many of its species are well known to be employed in the traditional medicines of many Asian countries. Some important conclusions on the chemotaxonomic and chemosystematic aspects of the genus have also been provided for the first time. Actually, this work represents the first total comprehensive review

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40

Wieczorek, Dorota, Beata Żyszka-Haberecht, Anna Kafka, and Jacek Lipok. "Phosphonates as Unique Components of Plant Seeds—A Promising Approach to Use Phosphorus Profiles in Plant Chemotaxonomy." International Journal of Molecular Sciences 22, no. 21 (2021): 11501. http://dx.doi.org/10.3390/ijms222111501.

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Phosphorus is one of the most important elements essential for all living beings. Plants accumulate and store phosphorous in various forms that have diverse physiological and biochemical functions. In this study, we determine and then examine the phosphorus profiles of seeds of plants belonging to different taxa based on extractable inorganic phosphates and organic forms of phosphorus. We paid particular attention to the presence of natural phosphonates in the tested materials. The inorganic phosphates were determined colorimetrically, whereas phosphorus profiles were created by using 31P NMR

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41

Aitzetmüller, Kurt. "Capillary GLC fatty acid fingerprints of seed lipids—a tool in plant chemotaxonomy?" Journal of High Resolution Chromatography 16, no. 8 (1993): 488–90. http://dx.doi.org/10.1002/jhrc.1240160809.

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42

Anuradha, S. M. J., B. K. Vijay Kumar, M. Radhakrishnaiah, and L. L. Narayana. "Chemotaxonomy of some species ofIndigofera L. With 5 tables." Feddes Repertorium 98, no. 9-10 (1987): 499–503. http://dx.doi.org/10.1002/fedr.4910980905.

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43

Serafini, Mauro, Antonella Piccin, Alessandra Stanzione, Valentina Petitto, and Marcello Nicoletti. "Chemotaxonomy of Linaria Genus by Nor-Iridoids Distribution." Natural Product Communications 3, no. 6 (2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300602.

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44

Rønsted, Nina, Edith Göbel, Henrik Franzyk, Søren Rosendal Jensen, and Carl Erik Olsen. "Chemotaxonomy of Plantago. Iridoid glucosides and caffeoyl phenylethanoid glycosides." Phytochemistry 55, no. 4 (2000): 337–48. http://dx.doi.org/10.1016/s0031-9422(00)00306-x.

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45

Mallavadhani, U. V., Anita K. Panda, and Y. R. Rao. "Review article number 134 pharmacology and chemotaxonomy of diospyros." Phytochemistry 49, no. 4 (1998): 901–51. http://dx.doi.org/10.1016/s0031-9422(97)01020-0.

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46

Máximo, Patrícia, Ana Lourenço, Andreas Tei, and Michael Wink. "Chemotaxonomy of Portuguese Ulex: Quinolizidine alkaloids as taxonomical markers." Phytochemistry 67, no. 17 (2006): 1943–49. http://dx.doi.org/10.1016/j.phytochem.2006.05.037.

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47

Wayman, Kjirsten A., Peter J. de Lange, Lesley Larsen, Catherine E. Sansom, and Nigel B. Perry. "Chemotaxonomy of Pseudowintera: Sesquiterpene dialdehyde variants are species markers." Phytochemistry 71, no. 7 (2010): 766–72. http://dx.doi.org/10.1016/j.phytochem.2010.01.017.

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48

Kilic, T., S. Carikci, G. Topcu, I. Aslan, and A. C. Goren. "Diterpenoids from Sideritis condensata. Evaluation of chemotaxonomy of Sideritis species and insecticidal activity." Chemistry of Natural Compounds 45, no. 6 (2009): 918–20. http://dx.doi.org/10.1007/s10600-010-9458-z.

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49

Pokhilo, N. D., A. K. Makhnev, and N. I. Uvarova. "Triterpenoids in leaves of Urals and Altai birches and questions of their chemotaxonomy." Chemistry of Natural Compounds 26, no. 2 (1990): 229–30. http://dx.doi.org/10.1007/bf00607559.

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50

Kalinin, Vladimir I., Alexandra S. Silchenko, Sergey A. Avilov, Valentin A. Stonik, and Alexey V. Smirnov. "Sea Cucumbers Triterpene Glycosides, the Recent Progress in Structural Elucidation and Chemotaxonomy." Phytochemistry Reviews 4, no. 2-3 (2005): 221–36. http://dx.doi.org/10.1007/s11101-005-1354-y.

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