Journal articles on the topic 'Plants Metabolism'

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1

Casanova-Sáez, Rubén, Eduardo Mateo-Bonmatí, and Karin Ljung. "Auxin Metabolism in Plants." Cold Spring Harbor Perspectives in Biology 13, no. 3 (January 11, 2021): a039867. http://dx.doi.org/10.1101/cshperspect.a039867.

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2

STEPAN-SARKISSIAN, G. "Carbohydrate Metabolism in Plants." Biochemical Society Transactions 13, no. 5 (October 1, 1985): 972. http://dx.doi.org/10.1042/bst0130972a.

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3

Witte, Claus-Peter, and Marco Herde. "Nucleotide Metabolism in Plants." Plant Physiology 182, no. 1 (October 22, 2019): 63–78. http://dx.doi.org/10.1104/pp.19.00955.

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4

Bedhomme, Mariette, Michaela Hoffmann, Erin A. McCarthy, Bernadette Gambonnet, Richard G. Moran, Fabrice Rébeillé, and Stéphane Ravanel. "Folate Metabolism in Plants." Journal of Biological Chemistry 280, no. 41 (July 29, 2005): 34823–31. http://dx.doi.org/10.1074/jbc.m506045200.

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5

Kennedy, Robert A., Mary E. Rumpho, and Theodore C. Fox. "Anaerobic Metabolism in Plants." Plant Physiology 100, no. 1 (September 1, 1992): 1–6. http://dx.doi.org/10.1104/pp.100.1.1.

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6

Harwood, John, and Thomas S. Moore. "Lipid metabolism in plants." Critical Reviews in Plant Sciences 8, no. 1 (January 1989): 1–43. http://dx.doi.org/10.1080/07352688909382269.

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7

Nisar, Nazia, Li Li, Shan Lu, Nay Chi Khin, and Barry J. Pogson. "Carotenoid Metabolism in Plants." Molecular Plant 8, no. 1 (January 2015): 68–82. http://dx.doi.org/10.1016/j.molp.2014.12.007.

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8

Gutbrod, Katharina, Jill Romer, and Peter Dörmann. "Phytol metabolism in plants." Progress in Lipid Research 74 (April 2019): 1–17. http://dx.doi.org/10.1016/j.plipres.2019.01.002.

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9

Witte, Claus-Peter. "Urea metabolism in plants." Plant Science 180, no. 3 (March 2011): 431–38. http://dx.doi.org/10.1016/j.plantsci.2010.11.010.

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10

Hill, Steven A. "Carbohydrate metabolism in plants." Trends in Plant Science 3, no. 10 (October 1998): 370–71. http://dx.doi.org/10.1016/s1360-1385(98)01320-x.

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11

Goddijn, O. "Trehalose metabolism in plants." Trends in Plant Science 4, no. 8 (August 1, 1999): 315–19. http://dx.doi.org/10.1016/s1360-1385(99)01446-6.

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12

Aspinall, Gerald O. "Carbohydrate metabolism in plants." Carbohydrate Research 135, no. 2 (January 1985): C23—C24. http://dx.doi.org/10.1016/s0008-6215(00)90792-4.

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13

HAYASHI, T., K. YOSHIDA, Y. WOOPARK, T. KONISHI, and K. BABA. "Cellulose Metabolism in Plants." International Review of Cytology 247 (2005): 1–34. http://dx.doi.org/10.1016/s0074-7696(05)47001-1.

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14

Zimmer, W., and R. Mendel. "Molybdenum Metabolism in Plants." Plant Biology 1, no. 2 (March 1999): 160–68. http://dx.doi.org/10.1111/j.1438-8677.1999.tb00239.x.

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15

Lunn, John Edward, Ines Delorge, Carlos María Figueroa, Patrick Van Dijck, and Mark Stitt. "Trehalose metabolism in plants." Plant Journal 79, no. 4 (May 21, 2014): 544–67. http://dx.doi.org/10.1111/tpj.12509.

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16

Kim, Hyun Uk. "Lipid Metabolism in Plants." Plants 9, no. 7 (July 9, 2020): 871. http://dx.doi.org/10.3390/plants9070871.

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In plants, lipids function in a variety of ways. Lipids are a major component of biological membranes and are used as a compact energy source for seed germination. Fatty acids, the major lipids in plants, are synthesized in plastid and assembled by glycerolipids or triacylglycerols in endoplasmic reticulum. The metabolism of fatty acids and triacylglycerols is well studied in most Arabidopsis model plants by forward and reverse genetics methods. However, research on the diverse functions of lipids in plants, including various crops, has yet to be completed. The papers of this Special Issue cover the core of the field of plant lipid research on the role of galactolipids in the chloroplast biogenesis from etioplasts and the role of acyltransferases and transcription factors involved in fatty acid and triacylglycerol synthesis. This information will contribute to the expansion of plant lipid research.
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17

Ravanel, Stéphane, Maryse A. Block, Pascal Rippert, Samuel Jabrin, Gilles Curien, Fabrice Rébeillé, and Roland Douce. "Methionine Metabolism in Plants." Journal of Biological Chemistry 279, no. 21 (March 15, 2004): 22548–57. http://dx.doi.org/10.1074/jbc.m313250200.

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18

Tejada-Jiménez, Manuel, Alejandro Chamizo-Ampudia, Aurora Galván, Emilio Fernández, and Ángel Llamas. "Molybdenum metabolism in plants." Metallomics 5, no. 9 (2013): 1191. http://dx.doi.org/10.1039/c3mt00078h.

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19

White, Philip J. "Selenium metabolism in plants." Biochimica et Biophysica Acta (BBA) - General Subjects 1862, no. 11 (November 2018): 2333–42. http://dx.doi.org/10.1016/j.bbagen.2018.05.006.

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20

Smith, Terence A. "Nitrogen metabolism of plants." Phytochemistry 33, no. 1 (April 1993): 251. http://dx.doi.org/10.1016/0031-9422(93)85438-w.

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21

Joshi, Vijay, and Alisdair R. Fernie. "Citrulline metabolism in plants." Amino Acids 49, no. 9 (July 25, 2017): 1543–59. http://dx.doi.org/10.1007/s00726-017-2468-4.

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22

Sembdner, G., C. Bruckner, A. Kehlen, H. D. Knofel, R. Kramell, A. Meyer, and O. Miersch. "METABOLISM OF JASMONATES IN PLANTS." Acta Horticulturae, no. 329 (January 1993): 205. http://dx.doi.org/10.17660/actahortic.1993.329.43.

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23

Bajguz, Andrzej. "Metabolism of brassinosteroids in plants." Plant Physiology and Biochemistry 45, no. 2 (February 2007): 95–107. http://dx.doi.org/10.1016/j.plaphy.2007.01.002.

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24

HAWKESFORD, MALCOLM J., and LUIT J. DE KOK. "Managing sulphur metabolism in plants." Plant, Cell and Environment 29, no. 3 (March 2006): 382–95. http://dx.doi.org/10.1111/j.1365-3040.2005.01470.x.

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25

Ito, Emi, Alan Crozier, and Hiroshi Ashihara. "Theophylline metabolism in higher plants." Biochimica et Biophysica Acta (BBA) - General Subjects 1336, no. 2 (August 1997): 323–30. http://dx.doi.org/10.1016/s0304-4165(97)00045-7.

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26

Loewus, Frank A., and Pushpalatha P. N. Murthy. "myo-Inositol metabolism in plants." Plant Science 150, no. 1 (January 2000): 1–19. http://dx.doi.org/10.1016/s0168-9452(99)00150-8.

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27

Garaita, Mercedes G., and John F. Kennedy. "Metabolism of Agrochemicals in Plants." Carbohydrate Polymers 46, no. 2 (October 2001): 196–97. http://dx.doi.org/10.1016/s0144-8617(01)00200-4.

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28

Andresen, Elisa, Edgar Peiter, and Hendrik Küpper. "Trace metal metabolism in plants." Journal of Experimental Botany 69, no. 5 (February 13, 2018): 909–54. http://dx.doi.org/10.1093/jxb/erx465.

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29

Ritsema, Tita, and Sjef C. M. Smeekens. "Engineering fructan metabolism in plants." Journal of Plant Physiology 160, no. 7 (January 2003): 811–20. http://dx.doi.org/10.1078/0176-1617-01029.

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30

Sandoval, Francisco J., Yi Zhang, and Sanja Roje. "Flavin Nucleotide Metabolism in Plants." Journal of Biological Chemistry 283, no. 45 (August 18, 2008): 30890–900. http://dx.doi.org/10.1074/jbc.m803416200.

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31

Tripathi, Bhumi Nath. "Editorial: Stress metabolism of plants." Protoplasma 245, no. 1-4 (August 28, 2010): 1. http://dx.doi.org/10.1007/s00709-010-0196-7.

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32

Benson, A. A., M. Katayama, and F. C. Knowles. "Arsenate metabolism in aquatic plants." Applied Organometallic Chemistry 2, no. 4 (1988): 349–52. http://dx.doi.org/10.1002/aoc.590020411.

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33

Azevedo, R. A., and P. J. Lea. "Lysine metabolism in higher plants." Amino Acids 20, no. 3 (April 12, 2001): 261–79. http://dx.doi.org/10.1007/s007260170043.

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34

Owusu Adjei, Mark, Xuzixin Zhou, Meiqin Mao, Fatima Rafique, and Jun Ma. "MicroRNAs Roles in Plants Secondary Metabolism." Plant Signaling & Behavior 16, no. 7 (May 3, 2021): 1915590. http://dx.doi.org/10.1080/15592324.2021.1915590.

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35

Van Eerd, Laura L., Robert E. Hoagland, Robert M. Zablotowicz, and J. Christopher Hall. "Pesticide metabolism in plants and microorganisms." Weed Science 51, no. 4 (July 2003): 472–95. http://dx.doi.org/10.1614/0043-1745(2003)051[0472:pmipam]2.0.co;2.

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36

Poirier, Yves, Aime Jaskolowski, and Joaquín Clúa. "Phosphate acquisition and metabolism in plants." Current Biology 32, no. 12 (June 2022): R623—R629. http://dx.doi.org/10.1016/j.cub.2022.03.073.

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37

Ashihara, Hiroshi. "Metabolism of alkaloids in coffee plants." Brazilian Journal of Plant Physiology 18, no. 1 (March 2006): 1–8. http://dx.doi.org/10.1590/s1677-04202006000100001.

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Coffee beans contain two types of alkaloids, caffeine and trigonelline, as major components. This review describes the distribution and metabolism of these compounds. Caffeine is synthesised from xanthosine derived from purine nucleotides. The major biosynthetic route is xanthosine -> 7-methylxanthosine -> 7-methylxanthine -> theobromine -> caffeine. Degradation activity of caffeine in coffee plants is very low, but catabolism of theophylline is always present. Theophylline is converted to xanthine, and then enters the conventional purine degradation pathway. A recent development in caffeine research is the successful cloning of genes of N-methyltransferases and characterization of recombinant proteins of these genes. Possible biotechnological applications are discussed briefly. Trigonelline (N-methylnicotinic acid) is synthesised from nicotinic acid derived from nicotinamide adenine nucleotides. Nicotinate N-methyltransferase (trigonelline synthase) activity was detected in coffee plants, but purification of this enzyme or cloning of the genes of this N-methyltransferase has not yet been reported. The degradation activity of trigonelline in coffee plants is extremely low.
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38

SEGUCHI, Kohichiroh, Sinichi SAKAI, Hisafumi KOBAYASI, and Yoshiroh KATOH. "Metabolism of Cycloprothrin in Rice Plants." Journal of Pesticide Science 16, no. 4 (1991): 599–607. http://dx.doi.org/10.1584/jpestics.16.599.

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39

Dennis, David T., and Maureen F. Greyson. "Fructose 6-phosphate metabolism in plants." Physiologia Plantarum 69, no. 2 (February 1987): 395–404. http://dx.doi.org/10.1111/j.1399-3054.1987.tb04306.x.

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40

Zhao, F. J., J. F. Ma, A. A. Meharg, and S. P. McGrath. "Arsenic uptake and metabolism in plants." New Phytologist 181, no. 4 (December 16, 2008): 777–94. http://dx.doi.org/10.1111/j.1469-8137.2008.02716.x.

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41

Gent, M. P. N. "Modeling translocation and metabolism in plants." Acta Horticulturae, no. 1271 (February 2020): 257–64. http://dx.doi.org/10.17660/actahortic.2020.1271.35.

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42

Jakubowski, Hieronim, and Andrzej Guranowski. "Metabolism of Homocysteine-thiolactone in Plants." Journal of Biological Chemistry 278, no. 9 (December 20, 2002): 6765–70. http://dx.doi.org/10.1074/jbc.m211819200.

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43

Spena, Angelo. "Transgenic plants altered in phytohormone metabolism." Acta Botanica Gallica 140, no. 6 (January 1993): 693–700. http://dx.doi.org/10.1080/12538078.1993.10515647.

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44

Stitt, Mark, and Uwe Sonnewald. "Regulation of Metabolism in Transgenic Plants." Annual Review of Plant Physiology and Plant Molecular Biology 46, no. 1 (June 1995): 341–68. http://dx.doi.org/10.1146/annurev.pp.46.060195.002013.

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45

Kotake, Toshihisa, Yukiko Yamanashi, Chiemi Imaizumi, and Yoichi Tsumuraya. "Metabolism of l-arabinose in plants." Journal of Plant Research 129, no. 5 (May 24, 2016): 781–92. http://dx.doi.org/10.1007/s10265-016-0834-z.

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46

Briat, Jean-François, Catherine Curie, and Frédéric Gaymard. "Iron utilization and metabolism in plants." Current Opinion in Plant Biology 10, no. 3 (June 2007): 276–82. http://dx.doi.org/10.1016/j.pbi.2007.04.003.

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47

Morikawa, Hiromichi, Misa Takahashi, Atsushi Sakamoto, Manami Ueda-Hashimoto, Toshiyuki Matsubara, Kazuhiro Miyawaki, Yoshifumi Kawamura, Toshifumi Hirata, and Hitomi Suzuki. "Novel Metabolism of Nitrogen in Plants." Zeitschrift für Naturforschung C 60, no. 3-4 (April 1, 2005): 265–71. http://dx.doi.org/10.1515/znc-2005-3-411.

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Abstract Our previous study showed that approximately one-third of the nitrogen of 15N-labeled NO2 taken up into plants was converted to a previously unknown organic nitrogen (hereafter designated UN) that was not recoverable by the Kjeldahl method (Morikawa et al., 2004). In this communication, we discuss metabolic and physiological relevance of the UN based on our newest experimental results. All of the 12 plant species were found to form UN derived from NO2 (about 10-30% of the total nitrogen derived from NO2). The UN was formed also from nitrate nitrogen in various plant species. Thus, UN is a common metabolite in plants. The amount of UN derived from NO2 was greatly increased in the transgenic tobacco clone 271 (Vaucheret et al., 1992) where the activity of nitrite reductase is suppressed less than 5% of that of the wild-type plant. On the other hand, the amount of this UN was significantly decreased by the overexpression of S-nitrosoglutathione reductase (GSNOR). These findings strongly suggest that nitrite and other reactive nitrogen species are involved in the formation of the UN, and that the UN-bearing compounds are metabolizable. A metabolic scheme for the formation of UN-bearing compounds was proposed, in which nitric oxide and peroxynitrite derived from NO2 or endogenous nitrogen oxides are involved for nitrosation and/or nitration of organic compounds in the cells to form nitroso and nitro compounds, including N-nitroso and S-nitroso ones. Participation of non-symbiotic haemoglobin bearing peroxidase-like activity (Sakamoto et al., 2004) and GSNOR (Sakamoto et al., 2002) in the metabolism of the UN was discussed. The UN-bearing compounds identified to date in the extracts of the leaves of Arabidopsis thaliana fumigated with NO2 include a ⊿2- 1,2,3-thiadiazoline derivative (Miyawaki et al., 2004) and 4-nitro-β-carotene.
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48

Sztein, A. Ester, Jerry D. Cohen, Janet P. Slovin, and Todd J. Cooke. "Auxin metabolism in representative land PLANTS." American Journal of Botany 82, no. 12 (December 1995): 1514–21. http://dx.doi.org/10.1002/j.1537-2197.1995.tb13853.x.

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49

Sieciechowicz, Konrad A., Kenneth W. Joy, and Robert J. Ireland. "The metabolism of asparagine in plants." Phytochemistry 27, no. 3 (January 1988): 663–71. http://dx.doi.org/10.1016/0031-9422(88)84071-8.

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50

BUTNARIU, Monica, and Nicolas-Sebastian BOCSO. "The biological role of primary and secondary plants metabolites." Nutrition and Food Processing 5, no. 3 (May 28, 2022): 01–07. http://dx.doi.org/10.31579/2637-8914/094.

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Metabolism consists of closely coordinated series of enzyme-mediated chemical reactions that take place in the plant organism, resulting in the synthesis and use of a wide variety of molecules in the category of carbohydrates, amino acids, fatty acids, nucleotides and polymers derived from them (polysaccharides, proteins, lipids, DNA, RNA, etc.). All these processes are defined as primary metabolism and the respective compounds, which are essential for the survival of the plant, are described as primary metabolites. In addition to the primary metabolites, which play a role in maintaining the viability of the plant (proteins, carbohydrates and lipids), a number of compounds such as terpenes, steroids, anthocyanins, anthraquinones, phenols and polyphenols, which belong to the "secondary metabolism", are also synthesized. Secondary metabolites (SMs) are present only in certain species, often manifesting specificity of organ or tissue, can be identified only at a certain stage of growth and development within a species, or can be activated only during periods of stress caused by the attack. microorganisms or nutrient depletion. Their synthesis seems to have no direct significance for the synthesizing cell, but may be decisive for the development and functioning of the body as a whole. Their synthesis is not a vital part of the gene expression and developmental program, these metabolites are not simple catabolic products, have a diversified structure and can be frequently re-included in metabolic processes. The boundary between primary and secondary metabolism is uncertain, as many primary metabolism intermediates play similar roles in secondary metabolism. Some obscure amino acids are infallibly SMs, while sterols are essential structural compounds of many organisms and should therefore be considered primary metabolites.
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