Research Article
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Year 2026, Volume: 54 Issue: 2 , 109 - 121 , 31.03.2026
https://doi.org/10.15671/hjbc.1754147
https://izlik.org/JA74LK28UY

Abstract

References

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  • R.S. Blosser, K.M. Gray, Extraction of violacein from Chromobacterium violaceum provides a new quantitative bioassay for N-acyl homoserine lactone autoinducers, J. Microbiol. Methods., 40 (2000) 47-55.
  • C. Sánchez, A.F. Braña, C. Méndez, J.A. Salas, Reevaluation of the violacein biosynthetic pathway and its relationship to indolocarbazole biosynthesis, Chembiochem, 7 (2006) 1231-1240.
  • N. Durán, G.Z. Justo, C.V. Ferreira, P.S. Melo, L. Cordi, D. Martins, Violacein: properties and biological activities, Biotechnol. Appl. Biochem., 48 (2007) 127-133.
  • M. Durán, A.N. Ponezi, A. Faljoni-Alario, M. F. S. Teixeira, G. Z. Justo, N. Durán, Potential applications of violacein: a microbial pigment, Med. Chem. Res., 21 (2012) 1524-1532.
  • F. Pantanella, F. Berlutti, C. Passariello, S. Sarli, C. Morea, S. Schippa, Violacein and biofilm production in Janthinobacterium lividum, J. Appl. Microbiol., 102 (2007) 992-999.
  • S. J. Kim, S.C. Shin, S.G. Hong, Y.M. Lee, H. Lee, J. Lee, I.G. Choi, H. Park, Genome sequence of Janthinobacterium sp. strain PAMC 25724, isolated from alpine glacier cryoconite, J. Bacteriol., 194 (2012) 2096.
  • C. Matz, P. Deines, J. Boenigk, H. Arndt, L. Eberl, S Kjelleberg, K. Jürgens, Impact of violacein–producing bacteria on survival and feeding of bacterivorous nanoflagellates, Appl. Environ. Microbiol., 70 (2004) 1593-1599.
  • C. R. Andrighetti-Fröhner, R.V. Antonio, T.B. Creczynski-Pasa, C.R. Barardi, C.M. Simões, Cytotoxicity and potential antiviral evaluation of violacein produced by Chromobacterium violaceum, Mem. Inst. Oswaldo Cruz, 98 (2003) 843-848.
  • K. I. Bektas, A. Nalcaoglu, H. Kati, E. Ceylan, R. Nalcacioglu, A.O.B. Belduz, S. Canakci, Janthinobacterium kumbetense sp. nov., a violacein-producing bacterium isolated from spring water in Turkey, and investigation of antimicrobial activity of violacein, FEMS Microbiol. Lett., 370 (2023) fnac119.
  • A.S. Mendes, J.E. de Carvalho, M.C.T. Duarte, N. Dur´an, R.E. Bruns, Factorial design and response surface optimization of crude violacein for Chromobacterium violaceum production, Biotechnol. Lett., 23 (2001) 1963-1969.
  • J.G. Cappuccino, N. Sherman, Microbiology: A Laboratory Manual (10th ed.), Pearson Education, 2014.
  • R.C. Kasana, R. Salwan, H. Dhar, S. Dutt, A. Gulati, A rapid and easy method for the detection of microbial cellulases on agar plates using gram's iodine, Curr. Microbiol., 57 (2008) 503-507.
  • W.K. Roberts, C.P. Selitrennikoff, Plant and Bacterial Chitinases Differ in Antifungal Activity, J. Fish Biol., 24 (1988) 125-134.
  • A.L. Barry, C. Thornsberry. Susceptibility testing in Lennette EH, Balows A, Hausler WJ, Truant JP, Manual of Clinical Microbiology, Washington, District of Columbia, American Society for Microbiology, (1981) 561-574.
  • CLSI. Performance Standards for Antimicrobial Susceptibility Testing. 33rd ed. CLSI supplement M100. Clinical and Laboratory Standards Institute, 2023.
  • S. Yada, Y. Wang, Y. Zou, K. Nagasaki, K. Hosokawa, I. Osaka, R. Arakawa, K. Enomoto, Isolation and characterization of two groups of novel marine bacteria producing violacein, Mar. Biotechnol., 10 (2008) 128-132.
  • E. Tomé, P. Teixeira, P.A. Gibbs, Anti-listerial inhibitory lactic acid bacteria isolated from commercial cold smoked salmon, Food Microbiol., 23 (2006) 399-405.
  • K. Shimada, K. Fujikawa, K. Yahara, T. Nakamura, Antioxidative properties of xanthan on the autoxidation of soybean oil in cyclodextrin emulsion, J. Agric. Food Chem., 40 (1992) 945-948.
  • Y.H. Kuo, H.C. Hsu, Y.C. Chen, T.W. Liang, S.L. Wang, A novel compound with antioxidant activity produced by Serrati aureilytica tku013, J. Agric. Food Chem., 60 (2012) 9043-9047.
  • M.B. Arnao, A. Cano, M. Acosta, The hydrophilic and lipophilic contribution to total antioxidant activity, Food Chem., 73 (2001) 239-244.
  • R.G. Birjandi, B. Shahnavaz, M. Bahreini, M.M. Tehran, Optimization of amylase enzyme production by a psychrothrophic Janthinobacterium sp. ATR812 with Response Surface Methodology, Appl. Biol., 31 (2018) 271-286.
  • S-ho. Park, S-ju. Park, Jong-il. Choi, Expression, Purification, and Characterization of a Cold-adapted Lipase from Janthinobacterium sp., Microbiol. Biotechnol. Lett., 46 (2018) 51-58.
  • H-do. Kim, J-il. Choi, Medium Optimization and Proteome Analysis of Protease Production by Janthinobacterium sp., Biotechnol. Bioprocess. Eng. 25 (2020) 787-794.
  • S-Gyui An, G.R. Ryu, Y-Su. Song, W-Jin. Jung, Properties of Chitinase-Producing Bacterium, Janthinobacterium agaricidamnosum AS-1 Isolated from Cryptotympana atrata, J. Chitin Chitosan Sci., 29 (2024) 122-128.
  • G.M. Rossolini, M.A. Condemi, F. Pantanella, J.D. Docquier, G. Amicosante, M.C. Thaller, Metallo-β-lactamase producers in environmental microbiota: New molecular class B enzyme in Janthinobacterium lividum, Antimicrob. Agents. Chemother., 45 (2001) 837-844.
  • Lu. Chernogor, K. Bakhvalova, A. Belikova, S. Belikov, Isolation and Properties of the Bacterial Strain Janthinobacterium sp. SLB01, Microorganisms, 10 (2022) 1071.
  • W.A. Ahmad, N.Z. Yusof, N. Nordin, Z.A. Zakaria, M.F. Rezali, Production and characterization of violacein by locally isolated Chromobacterium violaceum grown in agricultural wastes, Appl. Biochem. Biotechnol., 167 (2012) 1220-1234.
  • A. Baricz, A. Teban, C.M. Chiriac, E. Szekeres, A. Farkas, M. Nica, A. Dascălu, C. Oprișan, P. Lavin, C. Coman, Investigating the potential use of an antarctic variant of Janthinobacterium lividum for tackling antimicrobial resistance in a one health approach, Sci. Rep. 8 (2018) 1-12.
  • L.H. Yang, H. Xiong, O.O. Lee, S-H. Qi, P-Y. Qian, Effect of agitation on violacein production in Pseudoalteromonas luteoviolacea isolated from a marine sponge, Lett. Appl. Microbiol., 44 (2007) 625-630.
  • M. Kanelli, M. Mandic, M. Kalakona, S. Vasilakos, D. Kekos, J. Nikodinovic-Runic, E. Topakas, Microbial production of violacein and process optimization for dyeing polyamide fabrics with acquired antimicrobial properties, Front. Microbiol., 9 (2018) 1-12.
  • Y. Nakamura, C. Asada, T. Sawada. Production of antibacterial violet pigment by Psychrotropic bacterium RT102 strain, Biotechnol. Bioprocess Eng., 8 (2003) 37-40.
  • H. Wang, P. Jiang, Y. Lu, Z. Ruan, R. Jiang, X-H. Xing, K. Lou, D. Wei, Optimization of culture conditions for violacein production by a new strain of Duganella species B2, Biochem. Eng. J., 44 (2009) 119-124.
  • F. Khodaiyan, S.H. Razavi, Z. Emam-Djomeh, S.M.A. Mousavi, Optimization of canthaxanthin production by Dietzia natronolimnaea HS-1 using response surface methodology, Pak. J. Biol. Sci., 10 (2007) 2544-2552.
  • Y. Lu, L. Wang, Y. Xue, C. Zhang, X-H. Xing, K. Lou, Z. Zhang, Y. Li, G. Zhang, J. Bi, Z. Su, Production of violet pigment by a newly isolated psychrotrophic bacterium from a glacier in Xinjiang, China, Biochem. Eng. J., 43 (2009) 135-141.
  • J. Nomila Merlin, I.V.S. Nimal Christhudas, P. Praveen Kumar, P. Agastian, Optimization of growth and bioactive metabolite production: Fusarium solani, Asian J. Pharm. Clin. Res., 6 (2013) 98-103.
  • M.A. Palukurty, S.P. Pyla, S. Silarapu, S.R. Somalanka, Analyzing Alternative Nutrient Supplements and Optimization of Production Parameters for Violacein using Central Composite Design, Int. J. Eng., 7 (2016) 294-300.
  • S. Aranda, M. Montes-Borrego, B.B. Landa, Purple-pigmented violacein-producing Duganella spp. inhabits the rhizosphere of wild and cultivated olives in southern Spain, Microb. Ecol., 62 (2011) 446-459.
  • G. Sivarenjini, Production of violacein by a newly isolated bacterium Chromobacterium sp. JC1 (dissertation), Jawaharlal Nehru Technological University, 2011.
  • T.S. Vishnu, M. Palaniswamy, Impact of various fermentation conditions on the production of violacein by the novel isolate Chromobacterium vaccinii CV5, Int. J. Pharma Bio Sci., 8 (2017) 514-522.
  • M-Y. Fang, C. Zhang, S. Yang, J-Y. Cui, P-X. Jiang, K. Lou, M. Wachi, X-H. Xing, High crude violacein production from glucose by Escherichia coli engineered with interactive control of tryptophan pathway and violacein biosynthetic pathway, Microb. Cell Fact., 14 (2015) 1-13.
  • T.S. Vishnu, M. Palaniswamy, Systematic approach on evaluating the in vitro antioxidant activity of violacein; novel isolate Chromobacterium vaccinii CV5, Biomed. Pharmacol. J., 11 (2018) 703-709.
  • S. Nithiya, N. Karthik, J. Jayabharathi, In vitro antioxidant activity of hindered piperidone derivatives, Int. J. Pharm. Sci., 3 (2011) 254-256.

Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain

Year 2026, Volume: 54 Issue: 2 , 109 - 121 , 31.03.2026
https://doi.org/10.15671/hjbc.1754147
https://izlik.org/JA74LK28UY

Abstract

In this study, we aimed to screen for Janthinobacterium kumbetense GKT strain production of industrially important enzymes and to assess its antimicrobial resistance profile. Additionally, to enhance violacein production by GKT strain, we investigated the optimum cultivation conditions for this bacterium and the biological properties of crude violacein extract, including its antimicrobial and antioxidant activities. The GKT strain demonstrated proteolytic, lipolytic, and chitinolytic activities. Furthermore, the antibiotic susceptibility test showed that it was resistant to 5 out of the 15 antibiotics tested. Subsequently, the effects of different growth media, temperatures, pH levels, agitation rates, inoculum amounts, incubation times, carbon and nitrogen sources, and NaCl concentrations on violacein production by the GKT strain were examined. The maximum violacein yield of 28.7 μg/ml was achieved when the strain was incubated at 22°C for 72 hours under static conditions in nutrient broth with a pH of 6.4. Also, violacein yield increased with the addition of 1% pepton and 1% glucose as nitrogen and carbon sources, respectively. Violacein pigment, extracted using either methanol or ethanol, was found to inhibit the growth of S. aureus, S. epidermidis, B. cereus and E. faecalis. However, no-activity was seen on tested fungus strains. Additionally, violacein showed antioxidant activity against ABTS and DPPH radicals with IC50 values of 307 μg/ml and 261 μg/ml, respectively. Current research findings suggest that violacein pigment of GKT strain has potent antimicrobial and antioxidant activities and can be used in applications in the pharmaceutical industry.

Thanks

The authors gratefully acknowledge Prof. Dr. Berna Tunali (Department of Plant Protection, Faculty of Agriculture, Ondokuz Mayıs University) and Hatice Karadeniz (Giresun Food Control Laboratory) for providing the fungal isolates used in this study.

References

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  • R.S. Blosser, K.M. Gray, Extraction of violacein from Chromobacterium violaceum provides a new quantitative bioassay for N-acyl homoserine lactone autoinducers, J. Microbiol. Methods., 40 (2000) 47-55.
  • C. Sánchez, A.F. Braña, C. Méndez, J.A. Salas, Reevaluation of the violacein biosynthetic pathway and its relationship to indolocarbazole biosynthesis, Chembiochem, 7 (2006) 1231-1240.
  • N. Durán, G.Z. Justo, C.V. Ferreira, P.S. Melo, L. Cordi, D. Martins, Violacein: properties and biological activities, Biotechnol. Appl. Biochem., 48 (2007) 127-133.
  • M. Durán, A.N. Ponezi, A. Faljoni-Alario, M. F. S. Teixeira, G. Z. Justo, N. Durán, Potential applications of violacein: a microbial pigment, Med. Chem. Res., 21 (2012) 1524-1532.
  • F. Pantanella, F. Berlutti, C. Passariello, S. Sarli, C. Morea, S. Schippa, Violacein and biofilm production in Janthinobacterium lividum, J. Appl. Microbiol., 102 (2007) 992-999.
  • S. J. Kim, S.C. Shin, S.G. Hong, Y.M. Lee, H. Lee, J. Lee, I.G. Choi, H. Park, Genome sequence of Janthinobacterium sp. strain PAMC 25724, isolated from alpine glacier cryoconite, J. Bacteriol., 194 (2012) 2096.
  • C. Matz, P. Deines, J. Boenigk, H. Arndt, L. Eberl, S Kjelleberg, K. Jürgens, Impact of violacein–producing bacteria on survival and feeding of bacterivorous nanoflagellates, Appl. Environ. Microbiol., 70 (2004) 1593-1599.
  • C. R. Andrighetti-Fröhner, R.V. Antonio, T.B. Creczynski-Pasa, C.R. Barardi, C.M. Simões, Cytotoxicity and potential antiviral evaluation of violacein produced by Chromobacterium violaceum, Mem. Inst. Oswaldo Cruz, 98 (2003) 843-848.
  • K. I. Bektas, A. Nalcaoglu, H. Kati, E. Ceylan, R. Nalcacioglu, A.O.B. Belduz, S. Canakci, Janthinobacterium kumbetense sp. nov., a violacein-producing bacterium isolated from spring water in Turkey, and investigation of antimicrobial activity of violacein, FEMS Microbiol. Lett., 370 (2023) fnac119.
  • A.S. Mendes, J.E. de Carvalho, M.C.T. Duarte, N. Dur´an, R.E. Bruns, Factorial design and response surface optimization of crude violacein for Chromobacterium violaceum production, Biotechnol. Lett., 23 (2001) 1963-1969.
  • J.G. Cappuccino, N. Sherman, Microbiology: A Laboratory Manual (10th ed.), Pearson Education, 2014.
  • R.C. Kasana, R. Salwan, H. Dhar, S. Dutt, A. Gulati, A rapid and easy method for the detection of microbial cellulases on agar plates using gram's iodine, Curr. Microbiol., 57 (2008) 503-507.
  • W.K. Roberts, C.P. Selitrennikoff, Plant and Bacterial Chitinases Differ in Antifungal Activity, J. Fish Biol., 24 (1988) 125-134.
  • A.L. Barry, C. Thornsberry. Susceptibility testing in Lennette EH, Balows A, Hausler WJ, Truant JP, Manual of Clinical Microbiology, Washington, District of Columbia, American Society for Microbiology, (1981) 561-574.
  • CLSI. Performance Standards for Antimicrobial Susceptibility Testing. 33rd ed. CLSI supplement M100. Clinical and Laboratory Standards Institute, 2023.
  • S. Yada, Y. Wang, Y. Zou, K. Nagasaki, K. Hosokawa, I. Osaka, R. Arakawa, K. Enomoto, Isolation and characterization of two groups of novel marine bacteria producing violacein, Mar. Biotechnol., 10 (2008) 128-132.
  • E. Tomé, P. Teixeira, P.A. Gibbs, Anti-listerial inhibitory lactic acid bacteria isolated from commercial cold smoked salmon, Food Microbiol., 23 (2006) 399-405.
  • K. Shimada, K. Fujikawa, K. Yahara, T. Nakamura, Antioxidative properties of xanthan on the autoxidation of soybean oil in cyclodextrin emulsion, J. Agric. Food Chem., 40 (1992) 945-948.
  • Y.H. Kuo, H.C. Hsu, Y.C. Chen, T.W. Liang, S.L. Wang, A novel compound with antioxidant activity produced by Serrati aureilytica tku013, J. Agric. Food Chem., 60 (2012) 9043-9047.
  • M.B. Arnao, A. Cano, M. Acosta, The hydrophilic and lipophilic contribution to total antioxidant activity, Food Chem., 73 (2001) 239-244.
  • R.G. Birjandi, B. Shahnavaz, M. Bahreini, M.M. Tehran, Optimization of amylase enzyme production by a psychrothrophic Janthinobacterium sp. ATR812 with Response Surface Methodology, Appl. Biol., 31 (2018) 271-286.
  • S-ho. Park, S-ju. Park, Jong-il. Choi, Expression, Purification, and Characterization of a Cold-adapted Lipase from Janthinobacterium sp., Microbiol. Biotechnol. Lett., 46 (2018) 51-58.
  • H-do. Kim, J-il. Choi, Medium Optimization and Proteome Analysis of Protease Production by Janthinobacterium sp., Biotechnol. Bioprocess. Eng. 25 (2020) 787-794.
  • S-Gyui An, G.R. Ryu, Y-Su. Song, W-Jin. Jung, Properties of Chitinase-Producing Bacterium, Janthinobacterium agaricidamnosum AS-1 Isolated from Cryptotympana atrata, J. Chitin Chitosan Sci., 29 (2024) 122-128.
  • G.M. Rossolini, M.A. Condemi, F. Pantanella, J.D. Docquier, G. Amicosante, M.C. Thaller, Metallo-β-lactamase producers in environmental microbiota: New molecular class B enzyme in Janthinobacterium lividum, Antimicrob. Agents. Chemother., 45 (2001) 837-844.
  • Lu. Chernogor, K. Bakhvalova, A. Belikova, S. Belikov, Isolation and Properties of the Bacterial Strain Janthinobacterium sp. SLB01, Microorganisms, 10 (2022) 1071.
  • W.A. Ahmad, N.Z. Yusof, N. Nordin, Z.A. Zakaria, M.F. Rezali, Production and characterization of violacein by locally isolated Chromobacterium violaceum grown in agricultural wastes, Appl. Biochem. Biotechnol., 167 (2012) 1220-1234.
  • A. Baricz, A. Teban, C.M. Chiriac, E. Szekeres, A. Farkas, M. Nica, A. Dascălu, C. Oprișan, P. Lavin, C. Coman, Investigating the potential use of an antarctic variant of Janthinobacterium lividum for tackling antimicrobial resistance in a one health approach, Sci. Rep. 8 (2018) 1-12.
  • L.H. Yang, H. Xiong, O.O. Lee, S-H. Qi, P-Y. Qian, Effect of agitation on violacein production in Pseudoalteromonas luteoviolacea isolated from a marine sponge, Lett. Appl. Microbiol., 44 (2007) 625-630.
  • M. Kanelli, M. Mandic, M. Kalakona, S. Vasilakos, D. Kekos, J. Nikodinovic-Runic, E. Topakas, Microbial production of violacein and process optimization for dyeing polyamide fabrics with acquired antimicrobial properties, Front. Microbiol., 9 (2018) 1-12.
  • Y. Nakamura, C. Asada, T. Sawada. Production of antibacterial violet pigment by Psychrotropic bacterium RT102 strain, Biotechnol. Bioprocess Eng., 8 (2003) 37-40.
  • H. Wang, P. Jiang, Y. Lu, Z. Ruan, R. Jiang, X-H. Xing, K. Lou, D. Wei, Optimization of culture conditions for violacein production by a new strain of Duganella species B2, Biochem. Eng. J., 44 (2009) 119-124.
  • F. Khodaiyan, S.H. Razavi, Z. Emam-Djomeh, S.M.A. Mousavi, Optimization of canthaxanthin production by Dietzia natronolimnaea HS-1 using response surface methodology, Pak. J. Biol. Sci., 10 (2007) 2544-2552.
  • Y. Lu, L. Wang, Y. Xue, C. Zhang, X-H. Xing, K. Lou, Z. Zhang, Y. Li, G. Zhang, J. Bi, Z. Su, Production of violet pigment by a newly isolated psychrotrophic bacterium from a glacier in Xinjiang, China, Biochem. Eng. J., 43 (2009) 135-141.
  • J. Nomila Merlin, I.V.S. Nimal Christhudas, P. Praveen Kumar, P. Agastian, Optimization of growth and bioactive metabolite production: Fusarium solani, Asian J. Pharm. Clin. Res., 6 (2013) 98-103.
  • M.A. Palukurty, S.P. Pyla, S. Silarapu, S.R. Somalanka, Analyzing Alternative Nutrient Supplements and Optimization of Production Parameters for Violacein using Central Composite Design, Int. J. Eng., 7 (2016) 294-300.
  • S. Aranda, M. Montes-Borrego, B.B. Landa, Purple-pigmented violacein-producing Duganella spp. inhabits the rhizosphere of wild and cultivated olives in southern Spain, Microb. Ecol., 62 (2011) 446-459.
  • G. Sivarenjini, Production of violacein by a newly isolated bacterium Chromobacterium sp. JC1 (dissertation), Jawaharlal Nehru Technological University, 2011.
  • T.S. Vishnu, M. Palaniswamy, Impact of various fermentation conditions on the production of violacein by the novel isolate Chromobacterium vaccinii CV5, Int. J. Pharma Bio Sci., 8 (2017) 514-522.
  • M-Y. Fang, C. Zhang, S. Yang, J-Y. Cui, P-X. Jiang, K. Lou, M. Wachi, X-H. Xing, High crude violacein production from glucose by Escherichia coli engineered with interactive control of tryptophan pathway and violacein biosynthetic pathway, Microb. Cell Fact., 14 (2015) 1-13.
  • T.S. Vishnu, M. Palaniswamy, Systematic approach on evaluating the in vitro antioxidant activity of violacein; novel isolate Chromobacterium vaccinii CV5, Biomed. Pharmacol. J., 11 (2018) 703-709.
  • S. Nithiya, N. Karthik, J. Jayabharathi, In vitro antioxidant activity of hindered piperidone derivatives, Int. J. Pharm. Sci., 3 (2011) 254-256.
There are 43 citations in total.

Details

Primary Language English
Subjects Biochemistry and Cell Biology (Other)
Journal Section Research Article
Authors

Burak Karaca 0000-0003-2426-2622

Remziye Nalcacioglu 0000-0003-0527-9541

Hatice Katı 0000-0002-2053-3168

Submission Date July 31, 2025
Acceptance Date February 9, 2026
Publication Date March 31, 2026
DOI https://doi.org/10.15671/hjbc.1754147
IZ https://izlik.org/JA74LK28UY
Published in Issue Year 2026 Volume: 54 Issue: 2

Cite

APA Karaca, B., Nalcacioglu, R., & Katı, H. (2026). Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain. Hacettepe Journal of Biology and Chemistry, 54(2), 109-121. https://doi.org/10.15671/hjbc.1754147
AMA 1.Karaca B, Nalcacioglu R, Katı H. Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain. HJBC. 2026;54(2):109-121. doi:10.15671/hjbc.1754147
Chicago Karaca, Burak, Remziye Nalcacioglu, and Hatice Katı. 2026. “Biological Properties of Janthinobacterium Kumbetense Sp. Nov. (GKT) Strain and the Violacein Pigment Produced by This Locally Isolated Strain”. Hacettepe Journal of Biology and Chemistry 54 (2): 109-21. https://doi.org/10.15671/hjbc.1754147.
EndNote Karaca B, Nalcacioglu R, Katı H (March 1, 2026) Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain. Hacettepe Journal of Biology and Chemistry 54 2 109–121.
IEEE [1]B. Karaca, R. Nalcacioglu, and H. Katı, “Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain”, HJBC, vol. 54, no. 2, pp. 109–121, Mar. 2026, doi: 10.15671/hjbc.1754147.
ISNAD Karaca, Burak - Nalcacioglu, Remziye - Katı, Hatice. “Biological Properties of Janthinobacterium Kumbetense Sp. Nov. (GKT) Strain and the Violacein Pigment Produced by This Locally Isolated Strain”. Hacettepe Journal of Biology and Chemistry 54/2 (March 1, 2026): 109-121. https://doi.org/10.15671/hjbc.1754147.
JAMA 1.Karaca B, Nalcacioglu R, Katı H. Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain. HJBC. 2026;54:109–121.
MLA Karaca, Burak, et al. “Biological Properties of Janthinobacterium Kumbetense Sp. Nov. (GKT) Strain and the Violacein Pigment Produced by This Locally Isolated Strain”. Hacettepe Journal of Biology and Chemistry, vol. 54, no. 2, Mar. 2026, pp. 109-21, doi:10.15671/hjbc.1754147.
Vancouver 1.Burak Karaca, Remziye Nalcacioglu, Hatice Katı. Biological properties of Janthinobacterium kumbetense sp. nov. (GKT) strain and the violacein pigment produced by this locally isolated strain. HJBC. 2026 Mar. 1;54(2):109-21. doi:10.15671/hjbc.1754147

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