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1141por Rep Kaulić, Valentina, Racané, Livio, Leventić, Marijana, Šubarić, Domagoj, Rastija, Vesna, Glavaš-Obrovac, Ljubica, Raić-Malić, SilvanaEnlace del recurso
Publicado 2022
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1142“…RG11 roots secreted more oxalic acid and acetic acid and less tartaric acid, formic acid, malic acid, lactic acid, and succinic acid than Yuyan5 under Cd stress. …”
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1143por Slighoua, Meryem, Mahdi, Ismail, Moussaid, Fatima Zahrae, Kamaly, Omkulthom Al, Amrati, Fatima Ez-zahra, Conte, Raffaele, Drioiche, Aziz, Saleh, Asmaa, Housseini, Abdelilah Iraqi, Bari, Amina, Bousta, Dalila“…The LC-MS/MS showed that the hydro-ethanolic contains four polyphenols (oleuropein, arbutin, myricetin, and naringin) while GC-MS revealed that it contains 20 compounds including malic acid, D-glucose, and galactofuranoside. The hydro-ethanolic (1000 mg/kg) decreased abdominal writhes (38.96%) and licking time (37.34%). …”
Publicado 2023
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1144“…Furthermore, strain P10 biofilm formation was induced by malic acid, oxalic acid, and citric acid, whereas IAA secretion was promoted by the alanine, glycine, and proline in the peanut RE. …”
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1145“…Of these, the levels of 11 metabolites decreased (α-linolenic acid, prostaglandin E2, L-lactic acid, L-malic acid, 3-hydroxysebacic acid, succinyladenosine, guanosine, pyridoxal, L-glutamic acid, hippuric acid, and trigonelline), whereas the levels of the other 20 metabolites increased in the HC group with respect to the CON group (P < 0.05). …”
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1146por Haruma, Toshikatsu, Doyama, Kohei, Lu, Xingyan, Noji, Kenta, Masuya, Hayato, Arima, Takahiko, Tomiyama, Shingo, Yamaji, Keiko“…To adapt to the Fe stress environment, P. densiflora outside and inside the patches produced Fe detoxicants, including catechin, condensed tannin, and malic acid. Ceratobasidium bicorne and Aquapteridospora sp. were commonly isolated from P. densiflora seedlings outside and inside the patches as root endophytes, which might enhance Fe tolerance in the seedlings. …”
Publicado 2023
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1147por Zhong, Hua, Beaulaurier, John, Lum, Pek Yee, Molony, Cliona, Yang, Xia, MacNeil, Douglas J., Weingarth, Drew T., Zhang, Bin, Greenawalt, Danielle, Dobrin, Radu, Hao, Ke, Woo, Sangsoon, Fabre-Suver, Christine, Qian, Su, Tota, Michael R., Keller, Mark P., Kendziorski, Christina M., Yandell, Brian S., Castro, Victor, Attie, Alan D., Kaplan, Lee M., Schadt, Eric E.“…We identified and validated malic enzyme 1 (Me1) as a key regulator of this T2D subnetwork in mouse and provided support for the association of this gene to T2D in humans. …”
Publicado 2010
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1148por Rozhon, Wilfried, Wang, Wuyan, Berthiller, Franz, Mayerhofer, Juliane, Chen, Tingting, Petutschnig, Elena, Sieberer, Tobias, Poppenberger, Brigitte, Jonak, Claudia“…In addition, we provide evidence that iodobikinin and bikinin are inactivated in planta by conjugation with glutamic acid or malic acid and that the latter process is catalysed by the malate transferase SNG1. …”
Publicado 2014
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1149por Hamanishi, Erin T, Barchet, Genoa LH, Dauwe, Rebecca, Mansfield, Shawn D, Campbell, Malcolm M“…Notably, organic acid intermediates such as succinic and malic acid had lower concentrations in leaves exposed to drought, whereas galactinol and raffinose were found in increased concentrations. …”
Publicado 2015
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1150“…GK overexpression increased the total fatty acid content by 35 %, whereas G3PD1, G3PD2 and G3PD3 had no significant effect. Overexpression of malic enzyme (ME1) but not glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase or isocitrate dehydrogenase significantly increased fatty acid content when glycerol was used as carbon source. …”
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1151por Lehmann, Marco M., Wegener, Frederik, Barthel, Matti, Maurino, Veronica G., Siegwolf, Rolf T. W., Buchmann, Nina, Werner, Christiane, Werner, Roland A.“…In summary, our results suggest that respiration of both carboxyl groups of malate (via fumarase) by tricarboxylic acid cycle reactions or by NAD-malic enzyme influences δ(13)C(LEDR). The latter supplies the pyruvate dehydrogenase reaction, which in turn determines natural δ(13)C(LEDR) pattern by releasing the C-1 position of pyruvate.…”
Publicado 2016
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1152por de Oliveira Dal'Molin, Cristiana G., Orellana, Camila, Gebbie, Leigh, Steen, Jennifer, Hodson, Mark P., Chrysanthopoulos, Panagiotis, Plan, Manuel R., McQualter, Richard, Palfreyman, Robin W., Nielsen, Lars K.“…Besides revealing similarities and differences in central metabolism of mature and immature tissues, transcriptome analysis indicates significant gene expression of two malic enzyme isoforms (NADP- ME and NAD-ME). Although much greater expression levels of NADP-ME genes are observed and confirmed by the correspondent protein abundances in the samples, the expression of multiple genes combined to the significant abundance of metabolites that participates in C(4) metabolism of NAD-ME and NADP-ME subtypes suggest that S. italica may use mixed decarboxylation modes of C(4) photosynthetic pathways under different plant developmental stages. …”
Publicado 2016
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1153por Jalloh, Ibrahim, Helmy, Adel, Howe, Duncan J, Shannon, Richard J, Grice, Peter, Mason, Andrew, Gallagher, Clare N, Stovell, Matthew G, van der Heide, Susan, Murphy, Michael P, Pickard, John D, Menon, David K, Carpenter, T Adrian, Hutchinson, Peter J, Carpenter, Keri LH“…Metabolites 2,3-(13)C(2) malate and 2,3-(13)C(2) glutamine indicated tricarboxylic acid cycle metabolism, and 2,3-(13)C(2) lactate suggested tricarboxylic acid cycle spinout of pyruvate (by malic enzyme or phosphoenolpyruvate carboxykinase and pyruvate kinase), then lactate dehydrogenase-mediated conversion to lactate. …”
Publicado 2016
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1154por Koronowski, Kevin B., Khoury, Nathalie, Morris-Blanco, Kahlilia C., Stradecki-Cohan, Holly M., Garrett, Timothy J., Perez-Pinzon, Miguel A.“…Pathway and enrichment analysis of non-targeted primary metabolite profiles from Sirt5(−/−) cortex revealed alterations in several pathways including purine metabolism (urea, adenosine, adenine, xanthine), nitrogen metabolism (glutamic acid, glycine), and malate-aspartate shuttle (malic acid, glutamic acid). Additionally, perturbations in β-oxidation and carnitine transferase (pentadecanoic acid, heptadecanoic acid) and glutamate transport and glutamine synthetase (urea, xylitol, adenine, adenosine, glycine, glutamic acid) were predicted. …”
Publicado 2018
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1155por Lai, Biao, Du, Li-Na, Hu, Bing, Wang, Dan, Huang, Xu-Ming, Zhao, Jie-Tang, Wang, Hui-Cong, Hu, Gui-bing“…The expressions of LcMYB5 and its bHLH partner LcbHLH1 were consistent with the expression of putative tissue acidification gene LcPH1, and the changes in malic acid provided further evidence for the close relationship between LcMYB5 and tissue acidification. …”
Publicado 2019
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1156por Zamani, Arief Izzairy, Barig, Susann, Ibrahim, Sarah, Mohd. Yusof, Hirzun, Ibrahim, Julia, Low, Jaime Yoke Sum, Kua, Shwu Fun, Baharum, Syarul Nataqain, Stahmann, Klaus-Peter, Ng, Chyan Leong“…Significant differences in organic acids concentration of about 4- to 8-fold were observed for citric acid, succinic acid, malic acid, and oxaloacetic acid. Correlation of organic acids concentration and key enzymes involved in the central carbon metabolism was further determined by enzymatic assays. …”
Publicado 2020
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1157“…Further, gene expression analysis showed that pathways related to the production of substrates (acetyl-CoA and NADPH) for fatty acid synthesis (the branched-chain amino acid degradation pathway and the pentose phosphate pathway) and genes related to saturated fatty acid biosynthesis (the FAS pathway genes and malic enzyme) were, respectively, upregulated and downregulated. …”
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1158por Chatterjee, Jolly, Coe, Robert A, Acebron, Kelvin, Thakur, Vivek, Yennamalli, Ragothaman M, Danila, Florence, Lin, Hsiang-Chun, Balahadia, Christian Paolo, Bagunu, Efren, Padhma, Preiya P O S, Bala, Soumi, Yin, Xiaojia, Rizal, Govinda, Dionora, Jacqueline, Furbank, Robert T, von Caemmerer, Susanne, Quick, William Paul“…Changes in the abundance of other primary C(4) pathway enzymes were observed; accumulation of PEPC protein was significantly increased and accumulation of malate dehydrogenase and malic enzyme decreased. The reduction of CA protein activity and abundance in lcr1 restricts the supply of bicarbonate to PEPC, limiting C(4) photosynthesis and growth. …”
Publicado 2021
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1159por Israel, Liron L., Galstyan, Anna, Cox, Alysia, Shatalova, Ekaterina S., Sun, Tao, Rashid, Mohammad-Harun, Grodzinski, Zachary, Chiechi, Antonella, Fuchs, Dieu-Trang, Patil, Rameshwar, Koronyo-Hamaoui, Maya, Black, Keith L., Ljubimova, Julia Y., Holler, Eggehard“…Six peptide vectors were covalently attached to a 50 kDa poly(β-l-malic acid)-trileucine polymer forming P/LLL(40%)/vector conjugates. …”
Publicado 2022
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1160por Lovelace, Amelia H., Chen, Hsiao-Chun, Lee, Sangwook, Soufi, Ziad, Bota, Pedro, Preston, Gail M., Kvitko, Brian H.“…We identified rpoS-dependent alterations in the utilization of L-malic acid, an abundant carbon source in N. benthamiana apoplastic wash fluid. …”
Publicado 2022
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