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Effect of vanillic acid against oxidative stress induced by glyphosate in Saccharomyces cerevisiae

Year 2019, Volume: 12 Issue: 3, 34 - 43, 15.12.2019

Abstract

Glyphosate is a widely used broad-spectrum herbicide. Vanilic acid is a phenolic acid found naturally in many plants. In this study, the effect of vanilic acid against oxidative stress induced by glyphosate in Saccharomyces cerevisiae was investigated. S. cerevisiae was proliferated and developed in YEDP medium. Both glyphosate and vanilic acid were added to the development environment of Saccharomyces cerevisiae to be 200, 400 and 800 mg per liter. At the end of the experiment, Saccharomyces cerevisiae samples (Reduced glutathione (GSH), oxidized glutathione (GSSG), Malondialhedit (MDA), fatty acid, E, D, K vitamins and phytosterol) were analyzed in HPLC and GC devices. Antioxidant potential of vanillic acid was also identified. In this study, the effect of vanillic acid against oxidative stress and toxicity caused by glyphosate in S. cerevisiae was investigated for the first time. In S. cerevisiae administered glyphosate, there were statistically significant changes in MDA, GSH, GSSG, protein, fatty acid, E, D, K vitamins and phytosterol levels, but the vanilic acid applied was detected statistically significantly reduced the changes in these parameters. As a result of analysis by gas chromatography, the yeast cell of octanoic acid (8: 0), lauric acid (12: 0), myristic acid (14: 0), palmitic acid (16: 0), palmitoleic acid (16:1 n-7), stearic acid (18: 0), oleic acid (18:1 n-9) and linoleic acid (18:2 n-6) acids were observed. Vitamin D, E and K were analyzed with HPLC device. As a result of this analysis, molecules such as K2, δ-tocopherol, D2, D3, α-tocopherol, ergosterol, K1, stigmasterol, β-sitosterol were identified. Biochemical analysis showed that cell density in culture medium containing 800 mg per liter of glyphosate decreased. It was found that vanilic acid showed beneficial effects against oxidative stress caused by glyphosate in Saccharomyces cerevisiae.

References

  • Yılmaz, S., Aslım, B., & Beyatlı, Y. (1997). Glifosat herbisidinin bazı laktik asit bakterilerinin gelişimi ve asit üretimine etkisi. Tarım Bilimleri Dergisi, 3(3), 70-77.
  • Uren Webster, T.M., & Santos, E.M. (2015). Global transcriptomic profiling demonstrates induction of oxidative stress and of compensatory cellular stress responses in brown trout exposed to glyphosate and Roundup. BMC Genomics, 16:32. doi: 10.1186/s12864-015-1254-5.
  • Burella, P.M., Odetti, L.M., Simoniello, M.F., & Poletta, G.L. (2018). Oxidative damage and antioxidant defense in Caiman latirostris (Broad-snouted caiman) exposed in ovo to pesticide formulations. Ecotoxicol. Environ. Saf., 161, 437-443. doi: 10.1016/j.ecoenv.2018.06.006.
  • Gallegos, C.E., Baier, C.J., Bartos, M., Bras, C., Domínguez, S., Mónaco, N., … & Minetti, A. (2018). Perinatal glyphosate-based herbicide exposure in rats alters brain antioxidant status, glutamate and acetylcholine metabolism and affects recognition memory. Neurotox. Res., 34(3), 363-374. doi: 10.1007/s12640-018-9894-2.
  • Turkmen, R., Birdane, Y.O., Demirel, H.H., Yavuz, H., Kabu, M., & Ince, S. (2019). Antioxidant and cytoprotective effects of N-acetylcysteine against subchronic oral glyphosate-based herbicide-induced oxidative stress in rats. Environ. Sci. Pollut. Res. Int., 26(11),11427-11437. doi: 10.1007/s11356-019-04585-5.
  • Amin, F.U., Shah, S.A., & Kim, M.O. (2017). Vanillic acid attenuates Aβ1-42-induced oxidative stress and cognitive impairment in mice. Sci. Rep., 7, 40753. doi: 10.1038/srep40753.
  • Vinothiya, K., & Ashokkumar, N. (2017). Modulatory effect of vanillic acid on antioxidant status in high fat diet-induced changes in diabetic hypertensive rats. Biomed Pharmacother., 87, 640-652. doi: 10.1016/j.biopha.2016.12.134.
  • Brand-Williams, W., Cuvelier, M.E., & Berset, C. (1995). Use of a free radical method to evaluate antioxidant activity. LWT-Food Science and Technology, 28(1), 25-30.
  • Klejdus, B., Zehnálek, J., Adam, V., Petrek, J., Kizek, R., Vacek, J.,…& Kubán, V. (2004). Sub-picomole high-performance liquid chromatographic/mass spectrometric determination of glutathione in the maize (Zea mays L.) kernels exposed to cadmium. Analytica Chimica Acta, 520, 117-124. https://doi.org/10.1016/j.aca.2004.02.060
  • Yılmaz, O., Keser, S., Tuzcu, M., Güvenç, M., Çetintaş, B., Irtegun, S.,…& Şahin, K. (2009). A practical HPLC method to measure reduced (GSH) and oxidized (GSSG) glutathione concentrations in animal tissues. Journal of Animal Veterinary Advances, 8, 343-347.
  • Karatas, F., Karatepe, M., & Baysar, A. (2002). Determination of free malondialdehyde in human serum by high-performance liquid chromatography. Anal. Biochem., 311(1), 76-9.
  • Karatepe, M. (2004). Simultaneous determination of ascorbic acid and free malondialdehyde in human serum by HPLC/UV. LC-GC North America, 22(4), 362-365.
  • Hara, A., & Radin, N.S. (1978). Lipid extraction of tissues with a low-toxicity solvent. Anal. Biochem., 90(1), 420-6.
  • Christie, W.W. (1989). Gas chromatography and lipids. Glasgow: The Oily Press Ltd.
  • Tvrzická, E., Vecka, M., Staňková, B., & Žák, A. (2002). Analysis of fatty acids in plasma lipoproteins by gas chromatography–flame ionization detection: Quantitative aspects. Analytica Chimica Acta, 465, 337-350.
  • Katsanidis, E., & Addis, P.B. (1999). Novel HPLC analysis of tocopherols, tocotrienols, and cholesterol in tissue. Free Radic. Biol. Med., 27(11-12), 1137-40.
  • López-Cervantes, J., Sánchez-Machado, D.I., & Ríos-Vázquez, N.J. (2006). High-performance liquid chromatography method for the simultaneous quantification of retinol, alpha-tocopherol, and cholesterol in shrimp waste hydrolysate. J. Chromatogr. A., 1105(1-2), 135-9.
  • Braconi, D., Bernardini, G., Fiorani, M., Azzolini, C., Marzocchi, B., Proietti, F.,… & Santucci, A. (2010). Oxidative damage induced by herbicides is mediated by thiol oxidation and hydroperoxides production. Free. Radic. Res., 44(8), 891-906.
  • Luo, L., Wang, F., Zhang, Y., Zeng, M., Zhong, C., & Xiao, F. (2017). In vitro cytotoxicity assessment of roundup (glyphosate) in L-02 hepatocytes. J. Environ. Sci. Health B., 52(6), 410-417. doi: 10.1080/03601234.2017.1293449.
  • de Souza, J.S., Laureano-Melo, R., Herai, R.H., da Conceição, R.R., Oliveira, K.C., da Silva, I.D.C.G.,… & Giannocco, G. (2019). Maternal glyphosate-based herbicide exposure alters antioxidant-related genes in the brain and serum metabolites of male rat offspring. Neurotoxicology, 74, 121-131. doi: 10.1016/j.neuro.2019.06.004.
  • Gehin, A., Guyon, C., & Nicod, L. (2006). Glyphosate-induced antioxidant imbalance in HaCaT: The protective effect of vitamins C and E. Environ. Toxicol. Pharmacol., 22(1), 27-34. doi: 10.1016/j.etap.2005.11.003.
  • Kong, Z., Li, M., An, J., Chen, J., Bao, Y., Francis, F.,… & Dai, X. (2016). The fungicide triadimefon affects beer flavor and composition by influencing Saccharomyces cerevisiae metabolism. Sci. Rep., 6, 33552. doi: 10.1038/srep33552.
  • Peters, L.P., Carvalho, G., Martins, P.F., Dourado, M.N., Vilhena, M.B., Pileggi, M.,… & Azevedo, R.A. (2014). Differential responses of the antioxidant system of ametryn and clomazone tolerant bacteria. PLoS One, 9(11), e112271. doi: 10.1371/journal.pone.0112271.
  • Dianat, M., Radmanesh, E., Badavi, M., Mard, S.A., & Goudarzi, G. (2016). Disturbance effects of PM₁₀ on iNOS and eNOS mRNA expression levels and antioxidant activity induced by ischemia-reperfusion injury in isolated rat heart: protective role of vanillic acid. Environ. Sci. Pollut. Res. Int., 23(6), 5154-65. doi: 10.1007/s11356-015-5759-x.
  • Anbalagan, V., Raju, K., & Shanmugam, M. (2017). Assessment of lipid peroxidation and antioxidant status in vanillic acid treated 7,12-Dimethylbenz[a]anthracene induced hamster buccal pouch carcinogenesis. J. Clin. Diagn. Res., 11(3), BF01-BF04. doi: 10.7860/JCDR/2017/23537.9369.
  • Avdatek, F., Birdane, Y.O., Türkmen, R., & Demirel, H.H. (2018). Ameliorative effect of resveratrol on testicular oxidative stress, spermatological parameters and DNA damage in glyphosate-based herbicide-exposed rats. Andrologia, 50(7), e13036. doi: 10.1111/and.13036.
  • Hu, Z., He, B., Ma, L., Sun, Y., Niu, Y., & Zeng, B. (2017). Recent advances in ergosterol biosynthesis and regulation mechanisms in Saccharomyces cerevisiae. Indian J. Microbiol., 57(3), 270-277. doi: 10.1007/s12088-017-0657-1.
  • Kagan, I.A., Michel, A., Prause, A., Scheffler, B.E., Pace, P., & Duke, S.O. (2005). Gene transcription profiles of Saccharomyces cerevisiae after treatment with plant protection fungicides that inhibit ergosterol biosynthesis. Pesticide Biochemistry and Physiology, 82, 133–153. https://doi.org/10.1016/j.pestbp.2005.02.002
  • Bernat, P., Nykiel-Szymańska, J., Stolarek, P., Słaba, M., Szewczyk, R., & Różalska, S. (2018). 2,4-dichlorophenoxyacetic acid-induced oxidative stress: Metabolome and membrane modifications in Umbelopsis isabellina, a herbicide degrader. PLoS One, 13(6), e0199677. doi: 10.1371/journal.pone.0199677.
  • Viegas, C.A., Cabral, M.G., Teixeira, M.C., Neumann, G., Heipieper, H.J, & Sá-Correia, I. (2005). Yeast adaptation to 2,4-dichlorophenoxyacetic acid involves increased membrane fatty acid saturation degree and decreased OLE1 transcription. Biochem. Biophys. Res. Commun., 330(1), 271-8.
  • Tehlivets, O., Scheuringer, K., & Kohlwein, S.D. (2007). Fatty acid synthesis and elongation in yeast. Biochim. Biophys. Acta., 1771(3), 255-70.
  • Kieliszek, M., Błażejak, S., Bzducha-Wróbel, A., & Kot, A.M. (2019). Effect of selenium on lipid and amino acid metabolism in yeast cells. Biol. Trace Elem. Res., 187(1), 316-327. doi: 10.1007/s12011-018-1342-x.
  • Nakbi, A., Tayeb, W., Grissa, A., Issaoui, M., Dabbou, S., Chargui, I.,… & Hammami, M. (2010). Effects of olive oil and its fractions on oxidative stress and the liver's fatty acid composition in 2,4-Dichlorophenoxyacetic acid-treated rats. Nutr. Metab. (Lond.)., 7:80. doi: 10.1186/1743-7075-7-80.
  • Saxena, R., Garg, P., & Jain, D.K. (2011). In vitro anti-oxidant effect of vitamin e on oxidative stress induced due to pesticides in rat erythrocytes. Toxicol. Int., 18(1), 73-6. doi: 10.4103/0971-6580.75871.
  • Turkmen, R., Birdane, Y.O., Demirel, H.H., Kabu, M., & Ince, S. (2019). Protective effects of resveratrol on biomarkers of oxidative stress, biochemical and histopathological changes induced by sub-chronic oral glyphosate-based herbicide in rats. Toxicol. Res. (Camb.)., 8(2), 238-245. doi: 10.1039/c8tx00287h.
  • Okan, O.T., Varlıbaş, H., Öz, M., & Deniz, İ. (2013). Antioksidan analiz yöntemleri ve doğu Karadeniz bölgesinde antioksidan kaynağı olarak kullanılabilecek odun dışı bazı bitkisel ürünler. Kastamonu Üni., Orman Fakültesi Dergisi, 13(1), 48-59.
  • Kitiş, Y.E., Yazır, B., & Özkaya, H.Ö. (2016). The effects of some soil herbicides on root colonization and spore number of mycorrhizal fungi Glomus intraradice. Biological Diversity and Conservation, 9/2, 1-7.
  • Torretta, V., Katsoyiannis, I.A., Viotti, P., & Rada, E.C. (2018). Critical review of the effects of glyphosate exposure to the environment and humans through the food supply chain. Sustainability, 10, 950. doi:10.3390/su10040950.
  • Milić, M., Žunec, S., Micek, V., Kašuba, V., Mikolić, A., Lovaković B.T.,…& Želježić, D. (2018). Oxidative stress, cholinesterase activity, and DNA damage in the liver, whole blood, and plasma of Wistar rats following a 28-day exposure to glyphosate. Arh. Hig. Rada. Toksikol., 69, 154-168. doi: 10.2478/aiht-2018-69-3114

Glifosatın Saccharomyces cerevisiae’da indüklediği oksidatif strese karşı vanilik asidin etkisi

Year 2019, Volume: 12 Issue: 3, 34 - 43, 15.12.2019

Abstract

Glifosat, yaygın olarak kullanılan geniş spektrumlu bir herbisittir. Vanilik asit, pek çok bitkide doğal olarak bulunan fenolik asittir. Bu çalışmada, glifosatın Saccharomyces cerevisiae’da indüklediği oksidatif strese karşı vanilik asidin etkisi araştırılmıştır. S. cerevisiae YEDP besiyerinde çoğaltılmış ve geliştirilmiştir. Hem glifosat hem de vanilik asit Saccharomyces cerevisiae’nın gelişme ortamına litrede 200, 400 ve 800 mg olacak şekilde eklendi. Deney sonunda Saccharomyces cerevisiae örneklerinin analizleri (İndirgenmiş glutatyon (GSH), yükseltgenmiş glutatyon (GSSG), Malondialdehit (MDA), yağ asidi, E, D, K vitamin ve fitosterol) HPLC ve GC cihazlarında yapıldı. Ayrıca vanilik asidin antioksidan potansiyeli de tespit edildi. Bu çalışmada glifosatın S. cerevisiae’da oluşturduğu toksisite ve oksidatif strese karşı vanilik asidin etkisi ilk kez incelenmiştir. Glifosat uygulanan S. cerevisiae’da MDA, GSH, GSSG, protein, yağ asidi, E, D, K vitamin ve fitosterol düzeyinde istatistiksel olarak önemli değişikliklerin olduğu, fakat uygulanan vanilik asidin bu parametrelerde oluşan değişiklikleri istatistiksel olarak önemli ölçüde azalttığı tespit edildi. Gaz kromatografisi ile yapılan analiz sonucunda, maya hücresinde oktanoik asit (8:0), laurik asit (12:0), miristik asit (14:0), palmitik asit (16:0), palmitoleik asit (16:1 n-7), stearik asit (18:0), oleik asit (18:1 n-9) ve linoleik asit (18:2n-6) asitlerinin bulunduğu tespit edildi. D, E ve K vitamin miktarlarının analizi ise HPLC Cihazı ile yapıldı. Bu analiz sonucunda, K2, α-tokoferol, D2, D3, δ-tokoferol, ergosterol, K1, stigmasterol, β-sitosterol gibi moleküller tanımlandı. Biyokimyasal analizler sonucunda litrede 800 mg glifosat içeren kültür ortamındaki hücre yoğunluğunun azaldığı belirlendi. Glifosatın Saccharomyces cerevisiae'da oluşturduğu oksidatif strese karşı vanilik asidin faydalı etkiler gösterdiği tespit edildi.

References

  • Yılmaz, S., Aslım, B., & Beyatlı, Y. (1997). Glifosat herbisidinin bazı laktik asit bakterilerinin gelişimi ve asit üretimine etkisi. Tarım Bilimleri Dergisi, 3(3), 70-77.
  • Uren Webster, T.M., & Santos, E.M. (2015). Global transcriptomic profiling demonstrates induction of oxidative stress and of compensatory cellular stress responses in brown trout exposed to glyphosate and Roundup. BMC Genomics, 16:32. doi: 10.1186/s12864-015-1254-5.
  • Burella, P.M., Odetti, L.M., Simoniello, M.F., & Poletta, G.L. (2018). Oxidative damage and antioxidant defense in Caiman latirostris (Broad-snouted caiman) exposed in ovo to pesticide formulations. Ecotoxicol. Environ. Saf., 161, 437-443. doi: 10.1016/j.ecoenv.2018.06.006.
  • Gallegos, C.E., Baier, C.J., Bartos, M., Bras, C., Domínguez, S., Mónaco, N., … & Minetti, A. (2018). Perinatal glyphosate-based herbicide exposure in rats alters brain antioxidant status, glutamate and acetylcholine metabolism and affects recognition memory. Neurotox. Res., 34(3), 363-374. doi: 10.1007/s12640-018-9894-2.
  • Turkmen, R., Birdane, Y.O., Demirel, H.H., Yavuz, H., Kabu, M., & Ince, S. (2019). Antioxidant and cytoprotective effects of N-acetylcysteine against subchronic oral glyphosate-based herbicide-induced oxidative stress in rats. Environ. Sci. Pollut. Res. Int., 26(11),11427-11437. doi: 10.1007/s11356-019-04585-5.
  • Amin, F.U., Shah, S.A., & Kim, M.O. (2017). Vanillic acid attenuates Aβ1-42-induced oxidative stress and cognitive impairment in mice. Sci. Rep., 7, 40753. doi: 10.1038/srep40753.
  • Vinothiya, K., & Ashokkumar, N. (2017). Modulatory effect of vanillic acid on antioxidant status in high fat diet-induced changes in diabetic hypertensive rats. Biomed Pharmacother., 87, 640-652. doi: 10.1016/j.biopha.2016.12.134.
  • Brand-Williams, W., Cuvelier, M.E., & Berset, C. (1995). Use of a free radical method to evaluate antioxidant activity. LWT-Food Science and Technology, 28(1), 25-30.
  • Klejdus, B., Zehnálek, J., Adam, V., Petrek, J., Kizek, R., Vacek, J.,…& Kubán, V. (2004). Sub-picomole high-performance liquid chromatographic/mass spectrometric determination of glutathione in the maize (Zea mays L.) kernels exposed to cadmium. Analytica Chimica Acta, 520, 117-124. https://doi.org/10.1016/j.aca.2004.02.060
  • Yılmaz, O., Keser, S., Tuzcu, M., Güvenç, M., Çetintaş, B., Irtegun, S.,…& Şahin, K. (2009). A practical HPLC method to measure reduced (GSH) and oxidized (GSSG) glutathione concentrations in animal tissues. Journal of Animal Veterinary Advances, 8, 343-347.
  • Karatas, F., Karatepe, M., & Baysar, A. (2002). Determination of free malondialdehyde in human serum by high-performance liquid chromatography. Anal. Biochem., 311(1), 76-9.
  • Karatepe, M. (2004). Simultaneous determination of ascorbic acid and free malondialdehyde in human serum by HPLC/UV. LC-GC North America, 22(4), 362-365.
  • Hara, A., & Radin, N.S. (1978). Lipid extraction of tissues with a low-toxicity solvent. Anal. Biochem., 90(1), 420-6.
  • Christie, W.W. (1989). Gas chromatography and lipids. Glasgow: The Oily Press Ltd.
  • Tvrzická, E., Vecka, M., Staňková, B., & Žák, A. (2002). Analysis of fatty acids in plasma lipoproteins by gas chromatography–flame ionization detection: Quantitative aspects. Analytica Chimica Acta, 465, 337-350.
  • Katsanidis, E., & Addis, P.B. (1999). Novel HPLC analysis of tocopherols, tocotrienols, and cholesterol in tissue. Free Radic. Biol. Med., 27(11-12), 1137-40.
  • López-Cervantes, J., Sánchez-Machado, D.I., & Ríos-Vázquez, N.J. (2006). High-performance liquid chromatography method for the simultaneous quantification of retinol, alpha-tocopherol, and cholesterol in shrimp waste hydrolysate. J. Chromatogr. A., 1105(1-2), 135-9.
  • Braconi, D., Bernardini, G., Fiorani, M., Azzolini, C., Marzocchi, B., Proietti, F.,… & Santucci, A. (2010). Oxidative damage induced by herbicides is mediated by thiol oxidation and hydroperoxides production. Free. Radic. Res., 44(8), 891-906.
  • Luo, L., Wang, F., Zhang, Y., Zeng, M., Zhong, C., & Xiao, F. (2017). In vitro cytotoxicity assessment of roundup (glyphosate) in L-02 hepatocytes. J. Environ. Sci. Health B., 52(6), 410-417. doi: 10.1080/03601234.2017.1293449.
  • de Souza, J.S., Laureano-Melo, R., Herai, R.H., da Conceição, R.R., Oliveira, K.C., da Silva, I.D.C.G.,… & Giannocco, G. (2019). Maternal glyphosate-based herbicide exposure alters antioxidant-related genes in the brain and serum metabolites of male rat offspring. Neurotoxicology, 74, 121-131. doi: 10.1016/j.neuro.2019.06.004.
  • Gehin, A., Guyon, C., & Nicod, L. (2006). Glyphosate-induced antioxidant imbalance in HaCaT: The protective effect of vitamins C and E. Environ. Toxicol. Pharmacol., 22(1), 27-34. doi: 10.1016/j.etap.2005.11.003.
  • Kong, Z., Li, M., An, J., Chen, J., Bao, Y., Francis, F.,… & Dai, X. (2016). The fungicide triadimefon affects beer flavor and composition by influencing Saccharomyces cerevisiae metabolism. Sci. Rep., 6, 33552. doi: 10.1038/srep33552.
  • Peters, L.P., Carvalho, G., Martins, P.F., Dourado, M.N., Vilhena, M.B., Pileggi, M.,… & Azevedo, R.A. (2014). Differential responses of the antioxidant system of ametryn and clomazone tolerant bacteria. PLoS One, 9(11), e112271. doi: 10.1371/journal.pone.0112271.
  • Dianat, M., Radmanesh, E., Badavi, M., Mard, S.A., & Goudarzi, G. (2016). Disturbance effects of PM₁₀ on iNOS and eNOS mRNA expression levels and antioxidant activity induced by ischemia-reperfusion injury in isolated rat heart: protective role of vanillic acid. Environ. Sci. Pollut. Res. Int., 23(6), 5154-65. doi: 10.1007/s11356-015-5759-x.
  • Anbalagan, V., Raju, K., & Shanmugam, M. (2017). Assessment of lipid peroxidation and antioxidant status in vanillic acid treated 7,12-Dimethylbenz[a]anthracene induced hamster buccal pouch carcinogenesis. J. Clin. Diagn. Res., 11(3), BF01-BF04. doi: 10.7860/JCDR/2017/23537.9369.
  • Avdatek, F., Birdane, Y.O., Türkmen, R., & Demirel, H.H. (2018). Ameliorative effect of resveratrol on testicular oxidative stress, spermatological parameters and DNA damage in glyphosate-based herbicide-exposed rats. Andrologia, 50(7), e13036. doi: 10.1111/and.13036.
  • Hu, Z., He, B., Ma, L., Sun, Y., Niu, Y., & Zeng, B. (2017). Recent advances in ergosterol biosynthesis and regulation mechanisms in Saccharomyces cerevisiae. Indian J. Microbiol., 57(3), 270-277. doi: 10.1007/s12088-017-0657-1.
  • Kagan, I.A., Michel, A., Prause, A., Scheffler, B.E., Pace, P., & Duke, S.O. (2005). Gene transcription profiles of Saccharomyces cerevisiae after treatment with plant protection fungicides that inhibit ergosterol biosynthesis. Pesticide Biochemistry and Physiology, 82, 133–153. https://doi.org/10.1016/j.pestbp.2005.02.002
  • Bernat, P., Nykiel-Szymańska, J., Stolarek, P., Słaba, M., Szewczyk, R., & Różalska, S. (2018). 2,4-dichlorophenoxyacetic acid-induced oxidative stress: Metabolome and membrane modifications in Umbelopsis isabellina, a herbicide degrader. PLoS One, 13(6), e0199677. doi: 10.1371/journal.pone.0199677.
  • Viegas, C.A., Cabral, M.G., Teixeira, M.C., Neumann, G., Heipieper, H.J, & Sá-Correia, I. (2005). Yeast adaptation to 2,4-dichlorophenoxyacetic acid involves increased membrane fatty acid saturation degree and decreased OLE1 transcription. Biochem. Biophys. Res. Commun., 330(1), 271-8.
  • Tehlivets, O., Scheuringer, K., & Kohlwein, S.D. (2007). Fatty acid synthesis and elongation in yeast. Biochim. Biophys. Acta., 1771(3), 255-70.
  • Kieliszek, M., Błażejak, S., Bzducha-Wróbel, A., & Kot, A.M. (2019). Effect of selenium on lipid and amino acid metabolism in yeast cells. Biol. Trace Elem. Res., 187(1), 316-327. doi: 10.1007/s12011-018-1342-x.
  • Nakbi, A., Tayeb, W., Grissa, A., Issaoui, M., Dabbou, S., Chargui, I.,… & Hammami, M. (2010). Effects of olive oil and its fractions on oxidative stress and the liver's fatty acid composition in 2,4-Dichlorophenoxyacetic acid-treated rats. Nutr. Metab. (Lond.)., 7:80. doi: 10.1186/1743-7075-7-80.
  • Saxena, R., Garg, P., & Jain, D.K. (2011). In vitro anti-oxidant effect of vitamin e on oxidative stress induced due to pesticides in rat erythrocytes. Toxicol. Int., 18(1), 73-6. doi: 10.4103/0971-6580.75871.
  • Turkmen, R., Birdane, Y.O., Demirel, H.H., Kabu, M., & Ince, S. (2019). Protective effects of resveratrol on biomarkers of oxidative stress, biochemical and histopathological changes induced by sub-chronic oral glyphosate-based herbicide in rats. Toxicol. Res. (Camb.)., 8(2), 238-245. doi: 10.1039/c8tx00287h.
  • Okan, O.T., Varlıbaş, H., Öz, M., & Deniz, İ. (2013). Antioksidan analiz yöntemleri ve doğu Karadeniz bölgesinde antioksidan kaynağı olarak kullanılabilecek odun dışı bazı bitkisel ürünler. Kastamonu Üni., Orman Fakültesi Dergisi, 13(1), 48-59.
  • Kitiş, Y.E., Yazır, B., & Özkaya, H.Ö. (2016). The effects of some soil herbicides on root colonization and spore number of mycorrhizal fungi Glomus intraradice. Biological Diversity and Conservation, 9/2, 1-7.
  • Torretta, V., Katsoyiannis, I.A., Viotti, P., & Rada, E.C. (2018). Critical review of the effects of glyphosate exposure to the environment and humans through the food supply chain. Sustainability, 10, 950. doi:10.3390/su10040950.
  • Milić, M., Žunec, S., Micek, V., Kašuba, V., Mikolić, A., Lovaković B.T.,…& Želježić, D. (2018). Oxidative stress, cholinesterase activity, and DNA damage in the liver, whole blood, and plasma of Wistar rats following a 28-day exposure to glyphosate. Arh. Hig. Rada. Toksikol., 69, 154-168. doi: 10.2478/aiht-2018-69-3114
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Details

Primary Language Turkish
Subjects Conservation and Biodiversity
Journal Section Research Articles
Authors

Gözde Özcan This is me

Ersin Demir

Prof. Dr. Ökkeş Yılmaz

Figen Erdem Erişir This is me

Hatayi Zengin This is me

Publication Date December 15, 2019
Submission Date September 25, 2019
Acceptance Date December 15, 2019
Published in Issue Year 2019 Volume: 12 Issue: 3

Cite

APA Özcan, G., Demir, E., Yılmaz, P. D. . Ö., Erdem Erişir, F., et al. (2019). Glifosatın Saccharomyces cerevisiae’da indüklediği oksidatif strese karşı vanilik asidin etkisi. Biological Diversity and Conservation, 12(3), 34-43.

❖  Abstracted-Indexed in
Web of Science {Zoological Records Indexed] Clavariate Analytic, Medical Reads (RRS), CrossRef;10.46309/biodicon.

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Aberystwyth University; All libraries; Bath University; Birmingham University; Cardiff University; City University London; CONSER (Not UK Holdings); Edinburgh University; Essex University; Exeter University; Eskişehir Technical University Library; EZB Electronic Journals Library; Feng Chia University Library; GAZİ Gazi University Library; Glasgow University; HEC-National Digital Library; Hull University; Imperial College London; Kaohsinug Medical University Library; ANKOS; Anadolu University Library; Lancaster University; Libros PDF; Liverpool University; London Metropolitan University; London School of Economics and Political Science; Manchester University; National Cheng Kung University Library; National ILAN University Library; Nottingham University; Open University; Oxford University; Queen Mary,University of London;Robert Gordon University; Royal Botanic Gardens, Kew; Sheffield Hallam University; Sheffield University; Shih Hsin University Library; Smithsonian Institution Libraries; Southampton University; Stirling University; Strathclyde University; Sussex University; The National Agricultural Library (NAL); The Ohio Library and Information NetWork; Trinity College Dublin; University of Washington Libraries; Vaughan Memorial Library; York University..

❖ The article processing is free.

❖ Web of Science-Clarivate Analytics, Zoological Record
❖ This journal is a CrossRef;10.46309/biodicon. member

❖ Please visit ” http:// www.biodicon.com“ ; "https://dergipark.org.tr/en/pub/biodicon"   for instructions about articles and all of the details about journal


❖  Correspondance Adres: Prof. Ersin YÜCEL, Sazova Mahallesi, Ziraat Caddesi, No.277 F Blok, 26005 Tepebaşı-Eskişehir/Türkiye
E-posta / E-mail: biodicon@gmail.com;
Web Address: http://www.biodicon.com;   https://dergipark.org.tr/en/pub/biodicon
❖ Biological Diversity and Conservation/ Biyolojik Çeşitlilik ve Koruma
❖ ISSN 1308-5301 Print; ISSN 1308-8084 Online
❖ Start Date Published 2008
© Copyright by Biological Diversity and Conservation/Biyolojik Çeşitlilik ve Koruma-Available online at www.biodicon.com/All rights reserved
Publisher : ERSİN YÜCEL (https://www.ersinyucel.com.tr/)
❖ This journal is published three numbers in a year. Printed in Eskişehir/Türkiye.
❖ All sorts of responsibilities of the articles published in this journal are belonging to the authors
Editör / Editor-In-Chief : Prof.Dr. Ersin YÜCEL, https://orcid.org/0000-0001-8274-7578