Araştırma Makalesi
BibTex RIS Kaynak Göster
Yıl 2019, Cilt: 15 Sayı: 1, 87 - 94, 22.03.2019
https://doi.org/10.18466/cbayarfbe.475456

Öz

Kaynakça

  • 1. Hoiby, N, Bjarnsholt, T, Givskov, M, Molin, S, Ciofu, O. 2010. Antibiotic resistance of bacterial biofilms. International Journal of Antimicrobial Agents; 35: 322-332.
  • 2. Wright, GD. 2005. Bacterial resistance to antibiotics: Enzymatic degradation and modification. Advanced Drug Delivery Reviews; 57: 1451-1470.
  • 3. Fisher, JF, Meroueh, SO, Mobashery, S. 2011. Bacterial resistance to β-lactam antibiotics: compelling opportunism compelling opportunity, Chemical Reviews; 105: 395−424.
  • 4. Kuete, V, Alibert-Franco, S, Eyong, KO, Ngameni, B, Folefoc, GN, Nguemeving, JR. 2011. Antibacterial activity of some natural products against bacteria expressing a multidrug resistant phenotype, International Journal of Antimicrobial Agents; 37: 156-161.
  • 5. Stavri, M, Piddock, LJV, Gibbons, S. 2007. Bacterial efflux pump inhibitors from natural resources. Journal of Antimicrobial Chemotheraphy. 59(6): 1247-1260.
  • 6. Sun, J, Yin, Y, Sheng, GH, Yang, ZB, Zhu, HL. 2013. Synthesis, molecular modelling and structural characterization of vanillin derivatives as antimicrobial agents. Journal of Molecular Structure; 1039: 214-218.
  • 7. Harini, ST, Kumar, HV, Rangaswamy, J, Naik, N. 2012. Synthesis, antioxidant and antimicrobial activity of novel vanillin derived piperidin-4-one oxime esters: Preponderant role of the phenyl ester substituents on the piperidin-4-one oxime core. Bioorganic & Medicinal Chemistry Letters; 22: 7588-7592.
  • 8. Kamat, JP, Ghosh, A, Devasagayam, TPA. 2000. Vanillin as an antioxidant in rat liver mitochondria: Inhibition of protein oxidation and lipid peroxidation induced by photosensitization, Molecular and Cellular Biochemistry; 209:47-53.
  • 9. Naz, H, Tarique, M, Khan, P, Luqman, S, Ahamad, S, Islam, A, Ahmad, F, Hassan, MI. 2018. Evidence of vanillin binding to CAMKIV explains the anti-cancer mechanism in human hepatic carcinoma and neuroblastoma cells. Molecular and Cellular Biochemistry; 438: 35-45.
  • 10. Jung, HJ, Song, YS, Kim, K, Lim, CJ, Park, EH. 2010. Assessment of the anti-angiogenic, anti-inflammatory and anti-nociceptive properties of ethyl vanillin. Archives of Pharmacal Research; 33:309-316.
  • 11. King, AA, Shaughnessy, DT, Mure, K. 2007. Antimutagenicity of cinnamaldehyde and vanillin in human cells: Global gene expression and possible role of DNA damage and repair. Mutation Research; 616: 60-69.
  • 12. Segura, JL, Mancheno, MJ, Zamora, F. 2016. Covalent organic frameworks based on Schiff-base chemistry: synthesis, properties and potential applications. Chemical Society Reviews; 45: 5635-5671.
  • 13. Vitago, PA, Tamburini, S. 2004. The challenge of cyclic and acyclic schiff bases and related derivatives. Coordination Chemistry Reviews; 248: 1717-2128.
  • 14. Guerriero, P, Vigato, PA, Fenton, DE, Hellier, PC. 1992. Synthesis and Application of Macrocyclic and Macroactclic Schiff bases. Acta Chemica Scandinavica; 46: 1025-1046.
  • 15. Zayed, EM, Zayed, MA. 2015. Synthesis of novel schiff’s bases of highly potential biological activities and their structure investigation. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy; 143: 81-90.
  • 16. Ceylan, S. 2016. Synthesis and biological evaluation of new Mannich and Schiff bases containing 1,2,3-triazole and 1,3,4-oxadiazole nucleus. Medicinal Chemistry Research; 25: 1958-1970.
  • 17. Maja, M, Milan, C, Zrinusic, Z. 2012. Synthesis and antioxidant evaluation of Schiff bases derived from 2,6-pyridinedicarboxylic acid, Letters in Organic Chemistry; 9: 401-410.
  • 18. Gomez, RC, Witter, SK, Hieke, M. 2014. Vanillin-derived antiproliferative compounds influence Plk1 activity, Bioorganic and Medicinal Chemistry Letters; 24: 5063-5069.
  • 19. Engeland, M, Luc, JW, Frans, CS, Chris, PM. 1998. Annexin V-Affinity Assay: A Review on an Apoptosis Detection System Based on Phosphatidylserine Exposure. Cytometry; 31: 1-9.
  • 20. Faria, NCG, Kim, JH, Goncalves, LAP. 2011. Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus. Letters in Applied Microbiology; 52: 5.

Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives

Yıl 2019, Cilt: 15 Sayı: 1, 87 - 94, 22.03.2019
https://doi.org/10.18466/cbayarfbe.475456

Öz

Eleven vanillin derivatives was synthesized, characterized successfully
and their antibacterial and anticandidal properties were investigated on seven
bacterial species and four candida species. These bacterial species are
Staphylococcus aureus, Enterococcus faecalis, Listeria monocytogenes, Klebsiella pneumoniae, Pseudomonas aeruginosa, Escherichia coli, and Bacillus subtilis and candidal species
are
Candida albicans, Candida glabrata,
Candida krusei
and Candida
parapsilosis
. Most of the synthesized compounds were showed good activity
against studied microorganisms compared with Chloramphenicol. Compounds 2c, 2d
and 2k were exhibited remarkable antibacterial activities especially on
Escherichia coli. In addition, Klebsiella pneumoniae, Pseudomonas aeruginosa and Bacillus subtilis were found to be the
most susceptible species amongst the investigated microorganisms

Kaynakça

  • 1. Hoiby, N, Bjarnsholt, T, Givskov, M, Molin, S, Ciofu, O. 2010. Antibiotic resistance of bacterial biofilms. International Journal of Antimicrobial Agents; 35: 322-332.
  • 2. Wright, GD. 2005. Bacterial resistance to antibiotics: Enzymatic degradation and modification. Advanced Drug Delivery Reviews; 57: 1451-1470.
  • 3. Fisher, JF, Meroueh, SO, Mobashery, S. 2011. Bacterial resistance to β-lactam antibiotics: compelling opportunism compelling opportunity, Chemical Reviews; 105: 395−424.
  • 4. Kuete, V, Alibert-Franco, S, Eyong, KO, Ngameni, B, Folefoc, GN, Nguemeving, JR. 2011. Antibacterial activity of some natural products against bacteria expressing a multidrug resistant phenotype, International Journal of Antimicrobial Agents; 37: 156-161.
  • 5. Stavri, M, Piddock, LJV, Gibbons, S. 2007. Bacterial efflux pump inhibitors from natural resources. Journal of Antimicrobial Chemotheraphy. 59(6): 1247-1260.
  • 6. Sun, J, Yin, Y, Sheng, GH, Yang, ZB, Zhu, HL. 2013. Synthesis, molecular modelling and structural characterization of vanillin derivatives as antimicrobial agents. Journal of Molecular Structure; 1039: 214-218.
  • 7. Harini, ST, Kumar, HV, Rangaswamy, J, Naik, N. 2012. Synthesis, antioxidant and antimicrobial activity of novel vanillin derived piperidin-4-one oxime esters: Preponderant role of the phenyl ester substituents on the piperidin-4-one oxime core. Bioorganic & Medicinal Chemistry Letters; 22: 7588-7592.
  • 8. Kamat, JP, Ghosh, A, Devasagayam, TPA. 2000. Vanillin as an antioxidant in rat liver mitochondria: Inhibition of protein oxidation and lipid peroxidation induced by photosensitization, Molecular and Cellular Biochemistry; 209:47-53.
  • 9. Naz, H, Tarique, M, Khan, P, Luqman, S, Ahamad, S, Islam, A, Ahmad, F, Hassan, MI. 2018. Evidence of vanillin binding to CAMKIV explains the anti-cancer mechanism in human hepatic carcinoma and neuroblastoma cells. Molecular and Cellular Biochemistry; 438: 35-45.
  • 10. Jung, HJ, Song, YS, Kim, K, Lim, CJ, Park, EH. 2010. Assessment of the anti-angiogenic, anti-inflammatory and anti-nociceptive properties of ethyl vanillin. Archives of Pharmacal Research; 33:309-316.
  • 11. King, AA, Shaughnessy, DT, Mure, K. 2007. Antimutagenicity of cinnamaldehyde and vanillin in human cells: Global gene expression and possible role of DNA damage and repair. Mutation Research; 616: 60-69.
  • 12. Segura, JL, Mancheno, MJ, Zamora, F. 2016. Covalent organic frameworks based on Schiff-base chemistry: synthesis, properties and potential applications. Chemical Society Reviews; 45: 5635-5671.
  • 13. Vitago, PA, Tamburini, S. 2004. The challenge of cyclic and acyclic schiff bases and related derivatives. Coordination Chemistry Reviews; 248: 1717-2128.
  • 14. Guerriero, P, Vigato, PA, Fenton, DE, Hellier, PC. 1992. Synthesis and Application of Macrocyclic and Macroactclic Schiff bases. Acta Chemica Scandinavica; 46: 1025-1046.
  • 15. Zayed, EM, Zayed, MA. 2015. Synthesis of novel schiff’s bases of highly potential biological activities and their structure investigation. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy; 143: 81-90.
  • 16. Ceylan, S. 2016. Synthesis and biological evaluation of new Mannich and Schiff bases containing 1,2,3-triazole and 1,3,4-oxadiazole nucleus. Medicinal Chemistry Research; 25: 1958-1970.
  • 17. Maja, M, Milan, C, Zrinusic, Z. 2012. Synthesis and antioxidant evaluation of Schiff bases derived from 2,6-pyridinedicarboxylic acid, Letters in Organic Chemistry; 9: 401-410.
  • 18. Gomez, RC, Witter, SK, Hieke, M. 2014. Vanillin-derived antiproliferative compounds influence Plk1 activity, Bioorganic and Medicinal Chemistry Letters; 24: 5063-5069.
  • 19. Engeland, M, Luc, JW, Frans, CS, Chris, PM. 1998. Annexin V-Affinity Assay: A Review on an Apoptosis Detection System Based on Phosphatidylserine Exposure. Cytometry; 31: 1-9.
  • 20. Faria, NCG, Kim, JH, Goncalves, LAP. 2011. Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus. Letters in Applied Microbiology; 52: 5.
Toplam 20 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Hakan Ünver 0000-0002-4858-4039

Zerrin Cantürk

M. Güçlü Özarda Bu kişi benim

Yayımlanma Tarihi 22 Mart 2019
Yayımlandığı Sayı Yıl 2019 Cilt: 15 Sayı: 1

Kaynak Göster

APA Ünver, H., Cantürk, Z., & Özarda, M. G. (2019). Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives. Celal Bayar University Journal of Science, 15(1), 87-94. https://doi.org/10.18466/cbayarfbe.475456
AMA Ünver H, Cantürk Z, Özarda MG. Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives. CBUJOS. Mart 2019;15(1):87-94. doi:10.18466/cbayarfbe.475456
Chicago Ünver, Hakan, Zerrin Cantürk, ve M. Güçlü Özarda. “Evaluation of Antimicrobial Effect Against Some Microorganisms and Apoptotic Activity Against Candida Species of New Vanillin Derivatives”. Celal Bayar University Journal of Science 15, sy. 1 (Mart 2019): 87-94. https://doi.org/10.18466/cbayarfbe.475456.
EndNote Ünver H, Cantürk Z, Özarda MG (01 Mart 2019) Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives. Celal Bayar University Journal of Science 15 1 87–94.
IEEE H. Ünver, Z. Cantürk, ve M. G. Özarda, “Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives”, CBUJOS, c. 15, sy. 1, ss. 87–94, 2019, doi: 10.18466/cbayarfbe.475456.
ISNAD Ünver, Hakan vd. “Evaluation of Antimicrobial Effect Against Some Microorganisms and Apoptotic Activity Against Candida Species of New Vanillin Derivatives”. Celal Bayar University Journal of Science 15/1 (Mart 2019), 87-94. https://doi.org/10.18466/cbayarfbe.475456.
JAMA Ünver H, Cantürk Z, Özarda MG. Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives. CBUJOS. 2019;15:87–94.
MLA Ünver, Hakan vd. “Evaluation of Antimicrobial Effect Against Some Microorganisms and Apoptotic Activity Against Candida Species of New Vanillin Derivatives”. Celal Bayar University Journal of Science, c. 15, sy. 1, 2019, ss. 87-94, doi:10.18466/cbayarfbe.475456.
Vancouver Ünver H, Cantürk Z, Özarda MG. Evaluation of Antimicrobial Effect against Some Microorganisms and Apoptotic Activity against Candida Species of New Vanillin Derivatives. CBUJOS. 2019;15(1):87-94.