Carević, Milica

Link to this page

Authority KeyName Variants
orcid::0000-0002-2788-2432
  • Carević, Milica (5)
  • Carević, Milica B. (1)
Projects

Author's Bibliography

Enzymatic lipophilization of vitamin C with linoleic acid: Determination of antioxidant and diffusion properties of L-ascorbyl linoleate

Ćorović, Marija; Milivojević, Ana; Carević, Milica B.; Banjanac, Katarina; Vujisić, Ljubodrag V.; Pjanović, Rada V.; Bezbradica, Dejan

(2018)

TY  - JOUR
AU  - Ćorović, Marija
AU  - Milivojević, Ana
AU  - Carević, Milica B.
AU  - Banjanac, Katarina
AU  - Vujisić, Ljubodrag V.
AU  - Pjanović, Rada V.
AU  - Bezbradica, Dejan
PY  - 2018
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/217
AB  - Lipophilic derivatives of vitamin C are additives with antioxidant properties, attractive for application in food, cosmetics and pharmaceutics. They could be synthesized in lipase-catalyzed processes by using various acyl donors. Hereby, we present application of linoleic acid, which is polyunsaturated fatty acid essential in human nutrition, for esterification of vitamin C catalyzed by immobilized enzyme preparation Novozym® 435 in acetone. Highest specific ester yield, 9.7 mmol/g of immobilized lipase, was accomplished with 0.15 M of vitamin C, 0.6 M of linoleic acid, 3 g/l of enzyme and 0.07% (v/v) of water, at 60°C. NMR analyses of purified product proved that synthesized molecule was identical to 6-O-ascorbyl linoleate. Capacity of ester for scavenging 2,2-diphenyl-1-picrylhydrazyl radicals was two times higher comparing to parent molecule, vitamin C. Its diffusion coefficient, determined using Franz cell and cellulose acetate membrane, was 40% higher than palmitate and 62% higher than oleate. Obtained results showed that L-ascorbyl linoleate could be successfully synthesized in biocatalyzed processes. Furthermore, it was demonstrated that it possess high potential for application in different lipophilic products due to its liposolubility, high antioxidant efficiency and good diffusion properties.
AB  - Lipofilni derivati vitamina C su aditivi sa antioksidativnim dejstvom pogodni za primenu u prehrambenim, kozmetičkim i farmaceutskim proizvodima. Mogu biti sintetisani u procesima katalizovanim lipazama korišćenjem različitih acil-donora. U ovom radu, opisana je primena linolne kiseline, polinezasićene masne kiseline esencijalne u ljudskoj ishrani, u esterifikaciji vitamina C katalizovanoj imobilisanim enzimskim preparatom Novozym® 435 u acetonu. Najviši specifični prinos estra od 9,7 mmol/g imobilisane lipaze, ostvaren je sa 0,15 M vitamina C, 0,6 M linolne kiseline, 3 g/l enzima i 0,07 zapr. % vode, na 60°C. NMR analize prečišćenog proizvoda dokazale su da je sintetisani molekul identičan 6-O-askorbil-linolatu. Kapacitet estra za vezivanje 2,2- difenil-1-pikrilhidrazil radikala bio je dva puta viši u odnosu na sam vitamin C. Njegov koeficijent difuzije, određen korišćenjem Franz-ove ćelije i celuloza-acetatne membrane, bio je za 40% viši u odnosu na palmitat i za 62% u odnosu na oleat. Ostvareni rezultati pokazali su da L-askorbil-linolat može uspešno biti sintetisan u biokatalizovanom procesu. Pored toga, dokazano je da ovaj estar poseduje značajan potencijal za primenu u različitim lipofilnim proizvodima zbog svoje liposolubilnosti, snažnog antioksidativnog dejstva i pogodnih difuzionih karakteristika.
T2  - Food and Feed Research
T1  - Enzymatic lipophilization of vitamin C with linoleic acid: Determination of antioxidant and diffusion properties of L-ascorbyl linoleate
T1  - enzimska lipofilizacija vitamina C linolnom kiselinom - određivanje antioksidativnih i difuzionih svojstava L-askorbil-linolata
VL  - 45
IS  - 1
SP  - 1
EP  - 10
DO  - 10.5937/FFR1801001C
ER  - 
@article{
author = "Ćorović, Marija and Milivojević, Ana and Carević, Milica B. and Banjanac, Katarina and Vujisić, Ljubodrag V. and Pjanović, Rada V. and Bezbradica, Dejan",
year = "2018",
abstract = "Lipophilic derivatives of vitamin C are additives with antioxidant properties, attractive for application in food, cosmetics and pharmaceutics. They could be synthesized in lipase-catalyzed processes by using various acyl donors. Hereby, we present application of linoleic acid, which is polyunsaturated fatty acid essential in human nutrition, for esterification of vitamin C catalyzed by immobilized enzyme preparation Novozym® 435 in acetone. Highest specific ester yield, 9.7 mmol/g of immobilized lipase, was accomplished with 0.15 M of vitamin C, 0.6 M of linoleic acid, 3 g/l of enzyme and 0.07% (v/v) of water, at 60°C. NMR analyses of purified product proved that synthesized molecule was identical to 6-O-ascorbyl linoleate. Capacity of ester for scavenging 2,2-diphenyl-1-picrylhydrazyl radicals was two times higher comparing to parent molecule, vitamin C. Its diffusion coefficient, determined using Franz cell and cellulose acetate membrane, was 40% higher than palmitate and 62% higher than oleate. Obtained results showed that L-ascorbyl linoleate could be successfully synthesized in biocatalyzed processes. Furthermore, it was demonstrated that it possess high potential for application in different lipophilic products due to its liposolubility, high antioxidant efficiency and good diffusion properties., Lipofilni derivati vitamina C su aditivi sa antioksidativnim dejstvom pogodni za primenu u prehrambenim, kozmetičkim i farmaceutskim proizvodima. Mogu biti sintetisani u procesima katalizovanim lipazama korišćenjem različitih acil-donora. U ovom radu, opisana je primena linolne kiseline, polinezasićene masne kiseline esencijalne u ljudskoj ishrani, u esterifikaciji vitamina C katalizovanoj imobilisanim enzimskim preparatom Novozym® 435 u acetonu. Najviši specifični prinos estra od 9,7 mmol/g imobilisane lipaze, ostvaren je sa 0,15 M vitamina C, 0,6 M linolne kiseline, 3 g/l enzima i 0,07 zapr. % vode, na 60°C. NMR analize prečišćenog proizvoda dokazale su da je sintetisani molekul identičan 6-O-askorbil-linolatu. Kapacitet estra za vezivanje 2,2- difenil-1-pikrilhidrazil radikala bio je dva puta viši u odnosu na sam vitamin C. Njegov koeficijent difuzije, određen korišćenjem Franz-ove ćelije i celuloza-acetatne membrane, bio je za 40% viši u odnosu na palmitat i za 62% u odnosu na oleat. Ostvareni rezultati pokazali su da L-askorbil-linolat može uspešno biti sintetisan u biokatalizovanom procesu. Pored toga, dokazano je da ovaj estar poseduje značajan potencijal za primenu u različitim lipofilnim proizvodima zbog svoje liposolubilnosti, snažnog antioksidativnog dejstva i pogodnih difuzionih karakteristika.",
journal = "Food and Feed Research",
title = "Enzymatic lipophilization of vitamin C with linoleic acid: Determination of antioxidant and diffusion properties of L-ascorbyl linoleate, enzimska lipofilizacija vitamina C linolnom kiselinom - određivanje antioksidativnih i difuzionih svojstava L-askorbil-linolata",
volume = "45",
number = "1",
pages = "1-10",
doi = "10.5937/FFR1801001C"
}
Ćorović, M., Milivojević, A., Carević, M. B., Banjanac, K., Vujisić, L. V., Pjanović, R. V.,& Bezbradica, D.. (2018). Enzymatic lipophilization of vitamin C with linoleic acid: Determination of antioxidant and diffusion properties of L-ascorbyl linoleate. in Food and Feed Research, 45(1), 1-10.
https://doi.org/10.5937/FFR1801001C
Ćorović M, Milivojević A, Carević MB, Banjanac K, Vujisić LV, Pjanović RV, Bezbradica D. Enzymatic lipophilization of vitamin C with linoleic acid: Determination of antioxidant and diffusion properties of L-ascorbyl linoleate. in Food and Feed Research. 2018;45(1):1-10.
doi:10.5937/FFR1801001C .
Ćorović, Marija, Milivojević, Ana, Carević, Milica B., Banjanac, Katarina, Vujisić, Ljubodrag V., Pjanović, Rada V., Bezbradica, Dejan, "Enzymatic lipophilization of vitamin C with linoleic acid: Determination of antioxidant and diffusion properties of L-ascorbyl linoleate" in Food and Feed Research, 45, no. 1 (2018):1-10,
https://doi.org/10.5937/FFR1801001C . .
1
1

Supplementary data for article: Milivojević, A.; Ćorović, M.; Carevic, M.; Banjanac, K.; Vujisić, L. V.; Velickovic, D.; Bezbradica, D. Highly Efficient Enzymatic Acetylation of Flavonoids: Development of Solvent-Free Process and Kinetic Evaluation. Biochemical Engineering Journal 2017, 128, 106–115. https://doi.org/10.1016/j.bej.2017.09.018.

Milivojević, Ana; Ćorović, Marija; Carević, Milica; Banjanac, Katarina; Vujisić, Ljubodrag V.; Veličković, Dušan; Bezbradica, Dejan

(Elsevier Science Bv, Amsterdam, 2017)

TY  - DATA
AU  - Milivojević, Ana
AU  - Ćorović, Marija
AU  - Carević, Milica
AU  - Banjanac, Katarina
AU  - Vujisić, Ljubodrag V.
AU  - Veličković, Dušan
AU  - Bezbradica, Dejan
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2974
PB  - Elsevier Science Bv, Amsterdam
T2  - Biochemical Engineering Journal
T1  - Supplementary data for article: Milivojević, A.; Ćorović, M.; Carevic, M.; Banjanac, K.; Vujisić, L. V.; Velickovic, D.; Bezbradica, D. Highly Efficient Enzymatic Acetylation of Flavonoids: Development of Solvent-Free Process and Kinetic Evaluation. Biochemical Engineering Journal 2017, 128, 106–115. https://doi.org/10.1016/j.bej.2017.09.018.
UR  - https://hdl.handle.net/21.15107/rcub_cherry_2974
ER  - 
@misc{
author = "Milivojević, Ana and Ćorović, Marija and Carević, Milica and Banjanac, Katarina and Vujisić, Ljubodrag V. and Veličković, Dušan and Bezbradica, Dejan",
year = "2017",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Biochemical Engineering Journal",
title = "Supplementary data for article: Milivojević, A.; Ćorović, M.; Carevic, M.; Banjanac, K.; Vujisić, L. V.; Velickovic, D.; Bezbradica, D. Highly Efficient Enzymatic Acetylation of Flavonoids: Development of Solvent-Free Process and Kinetic Evaluation. Biochemical Engineering Journal 2017, 128, 106–115. https://doi.org/10.1016/j.bej.2017.09.018.",
url = "https://hdl.handle.net/21.15107/rcub_cherry_2974"
}
Milivojević, A., Ćorović, M., Carević, M., Banjanac, K., Vujisić, L. V., Veličković, D.,& Bezbradica, D.. (2017). Supplementary data for article: Milivojević, A.; Ćorović, M.; Carevic, M.; Banjanac, K.; Vujisić, L. V.; Velickovic, D.; Bezbradica, D. Highly Efficient Enzymatic Acetylation of Flavonoids: Development of Solvent-Free Process and Kinetic Evaluation. Biochemical Engineering Journal 2017, 128, 106–115. https://doi.org/10.1016/j.bej.2017.09.018.. in Biochemical Engineering Journal
Elsevier Science Bv, Amsterdam..
https://hdl.handle.net/21.15107/rcub_cherry_2974
Milivojević A, Ćorović M, Carević M, Banjanac K, Vujisić LV, Veličković D, Bezbradica D. Supplementary data for article: Milivojević, A.; Ćorović, M.; Carevic, M.; Banjanac, K.; Vujisić, L. V.; Velickovic, D.; Bezbradica, D. Highly Efficient Enzymatic Acetylation of Flavonoids: Development of Solvent-Free Process and Kinetic Evaluation. Biochemical Engineering Journal 2017, 128, 106–115. https://doi.org/10.1016/j.bej.2017.09.018.. in Biochemical Engineering Journal. 2017;.
https://hdl.handle.net/21.15107/rcub_cherry_2974 .
Milivojević, Ana, Ćorović, Marija, Carević, Milica, Banjanac, Katarina, Vujisić, Ljubodrag V., Veličković, Dušan, Bezbradica, Dejan, "Supplementary data for article: Milivojević, A.; Ćorović, M.; Carevic, M.; Banjanac, K.; Vujisić, L. V.; Velickovic, D.; Bezbradica, D. Highly Efficient Enzymatic Acetylation of Flavonoids: Development of Solvent-Free Process and Kinetic Evaluation. Biochemical Engineering Journal 2017, 128, 106–115. https://doi.org/10.1016/j.bej.2017.09.018." in Biochemical Engineering Journal (2017),
https://hdl.handle.net/21.15107/rcub_cherry_2974 .

Highly efficient enzymatic acetylation of flavonoids: Development of solvent-free process and kinetic evaluation

Milivojević, Ana; Ćorović, Marija; Carević, Milica; Banjanac, Katarina; Vujisić, Ljubodrag V.; Veličković, Dušan; Bezbradica, Dejan

(Elsevier Science Bv, Amsterdam, 2017)

TY  - JOUR
AU  - Milivojević, Ana
AU  - Ćorović, Marija
AU  - Carević, Milica
AU  - Banjanac, Katarina
AU  - Vujisić, Ljubodrag V.
AU  - Veličković, Dušan
AU  - Bezbradica, Dejan
PY  - 2017
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2558
AB  - Solubility and stability of flavonoid glycosides, valuable natural constituents of cosmetics and pharmaceuticals, could be improved by lipase-catalyzed acylation. Focus of this study was on development of eco-friendly process for the production of flavonoid acetates. By using phloridzin as model compound and triacetin as acetyl donor and solvent, 100% conversion and high productivity (23.32 gl(-1) day(-1)) were accomplished. Complete conversions of two other glycosylated flavonoids, naringin and esculin, in solvent-free system were achieved, as well. Comprehensive kinetic mechanism based on two con-secutive mono-substrate reactions was established where first one represents formation of flavonoid monoacetate and within second reaction diacetate is being produced from monoacetate. Both steps were regarded as reversible Michaelis-Menten reactions without inhibition. Apparent kinetic parameters for two consecutive reactions (V-m constants for substrates and products and Km constants for forward and reverse reactions) were estimated for three examined acetyl acceptors and excellent fitting of experimental data (R-2 gt 0.97) was achieved. Obtained results showed that derived kinetic model could be applicable for solvent-free esterifications of different flavonoid glycosides. It was valid for entire transesterification course (72 h of reaction) which, combined with complete conversions and green character of synthesis, represents firm basis for further process development. (C) 2017 Elsevier B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Biochemical Engineering Journal
T1  - Highly efficient enzymatic acetylation of flavonoids: Development of solvent-free process and kinetic evaluation
VL  - 128
SP  - 106
EP  - 115
DO  - 10.1016/j.bej.2017.09.018
ER  - 
@article{
author = "Milivojević, Ana and Ćorović, Marija and Carević, Milica and Banjanac, Katarina and Vujisić, Ljubodrag V. and Veličković, Dušan and Bezbradica, Dejan",
year = "2017",
abstract = "Solubility and stability of flavonoid glycosides, valuable natural constituents of cosmetics and pharmaceuticals, could be improved by lipase-catalyzed acylation. Focus of this study was on development of eco-friendly process for the production of flavonoid acetates. By using phloridzin as model compound and triacetin as acetyl donor and solvent, 100% conversion and high productivity (23.32 gl(-1) day(-1)) were accomplished. Complete conversions of two other glycosylated flavonoids, naringin and esculin, in solvent-free system were achieved, as well. Comprehensive kinetic mechanism based on two con-secutive mono-substrate reactions was established where first one represents formation of flavonoid monoacetate and within second reaction diacetate is being produced from monoacetate. Both steps were regarded as reversible Michaelis-Menten reactions without inhibition. Apparent kinetic parameters for two consecutive reactions (V-m constants for substrates and products and Km constants for forward and reverse reactions) were estimated for three examined acetyl acceptors and excellent fitting of experimental data (R-2 gt 0.97) was achieved. Obtained results showed that derived kinetic model could be applicable for solvent-free esterifications of different flavonoid glycosides. It was valid for entire transesterification course (72 h of reaction) which, combined with complete conversions and green character of synthesis, represents firm basis for further process development. (C) 2017 Elsevier B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Biochemical Engineering Journal",
title = "Highly efficient enzymatic acetylation of flavonoids: Development of solvent-free process and kinetic evaluation",
volume = "128",
pages = "106-115",
doi = "10.1016/j.bej.2017.09.018"
}
Milivojević, A., Ćorović, M., Carević, M., Banjanac, K., Vujisić, L. V., Veličković, D.,& Bezbradica, D.. (2017). Highly efficient enzymatic acetylation of flavonoids: Development of solvent-free process and kinetic evaluation. in Biochemical Engineering Journal
Elsevier Science Bv, Amsterdam., 128, 106-115.
https://doi.org/10.1016/j.bej.2017.09.018
Milivojević A, Ćorović M, Carević M, Banjanac K, Vujisić LV, Veličković D, Bezbradica D. Highly efficient enzymatic acetylation of flavonoids: Development of solvent-free process and kinetic evaluation. in Biochemical Engineering Journal. 2017;128:106-115.
doi:10.1016/j.bej.2017.09.018 .
Milivojević, Ana, Ćorović, Marija, Carević, Milica, Banjanac, Katarina, Vujisić, Ljubodrag V., Veličković, Dušan, Bezbradica, Dejan, "Highly efficient enzymatic acetylation of flavonoids: Development of solvent-free process and kinetic evaluation" in Biochemical Engineering Journal, 128 (2017):106-115,
https://doi.org/10.1016/j.bej.2017.09.018 . .
17
7
15
13

Immobilization of maltase from Saccharomyces cerevisiae on thiosulfonate supports

Mihailović, Mladen; Trbojević-Ivić, Jovana; Banjanac, Katarina; Milosavić, Nenad; Veličković, Dušan; Carević, Milica; Bezbradica, Dejan

(Serbian Chemical Soc, Belgrade, 2016)

TY  - JOUR
AU  - Mihailović, Mladen
AU  - Trbojević-Ivić, Jovana
AU  - Banjanac, Katarina
AU  - Milosavić, Nenad
AU  - Veličković, Dušan
AU  - Carević, Milica
AU  - Bezbradica, Dejan
PY  - 2016
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2391
AB  - In this study, two commercial supports (Eupergit (R) C and Purolite (R) A109) were chemically modified in order to introduce thiosulfonate groups, which could subsequently exclusively react with the cysteine residues on the surface of enzymes. Thereafter, the maltase from Saccharomyces cerevisiae was immobilized onto the obtained thiosulfonate-activated supports, resulting in high expressed enzymatic activities (around 50 %), while on the other hand, immobilization on unmodified supports yielded expressed activities less than 5 %. Moreover, protein loadings up to 12.3 mg g(-1) and immobilized activities up to 3580 IU g(-1) were achieved by employment of these thiosulfonate supports. Desorption experiments, performed on samples taken during immobilization, proved that immobilization on the thiosulfonate supports was the first step of fast adsorption onto the supports and the formation of covalent bonds between the thiosulfonate groups and the thiol groups of cysteine represented a second slower step. More importantly, although enzyme coupling occurred via covalent bond formation, the performed immobilization proved to be reversible, since it was shown that 95 % of the immobilized activity could be detached from the support after treatment with a thiol reagent (beta-mercaptoethanol). Thus, the support could be reused after enzyme inactivation.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Immobilization of maltase from Saccharomyces cerevisiae on thiosulfonate supports
VL  - 81
IS  - 12
SP  - 1371
EP  - 1382
DO  - 10.2298/JSC160730099M
ER  - 
@article{
author = "Mihailović, Mladen and Trbojević-Ivić, Jovana and Banjanac, Katarina and Milosavić, Nenad and Veličković, Dušan and Carević, Milica and Bezbradica, Dejan",
year = "2016",
abstract = "In this study, two commercial supports (Eupergit (R) C and Purolite (R) A109) were chemically modified in order to introduce thiosulfonate groups, which could subsequently exclusively react with the cysteine residues on the surface of enzymes. Thereafter, the maltase from Saccharomyces cerevisiae was immobilized onto the obtained thiosulfonate-activated supports, resulting in high expressed enzymatic activities (around 50 %), while on the other hand, immobilization on unmodified supports yielded expressed activities less than 5 %. Moreover, protein loadings up to 12.3 mg g(-1) and immobilized activities up to 3580 IU g(-1) were achieved by employment of these thiosulfonate supports. Desorption experiments, performed on samples taken during immobilization, proved that immobilization on the thiosulfonate supports was the first step of fast adsorption onto the supports and the formation of covalent bonds between the thiosulfonate groups and the thiol groups of cysteine represented a second slower step. More importantly, although enzyme coupling occurred via covalent bond formation, the performed immobilization proved to be reversible, since it was shown that 95 % of the immobilized activity could be detached from the support after treatment with a thiol reagent (beta-mercaptoethanol). Thus, the support could be reused after enzyme inactivation.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Immobilization of maltase from Saccharomyces cerevisiae on thiosulfonate supports",
volume = "81",
number = "12",
pages = "1371-1382",
doi = "10.2298/JSC160730099M"
}
Mihailović, M., Trbojević-Ivić, J., Banjanac, K., Milosavić, N., Veličković, D., Carević, M.,& Bezbradica, D.. (2016). Immobilization of maltase from Saccharomyces cerevisiae on thiosulfonate supports. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 81(12), 1371-1382.
https://doi.org/10.2298/JSC160730099M
Mihailović M, Trbojević-Ivić J, Banjanac K, Milosavić N, Veličković D, Carević M, Bezbradica D. Immobilization of maltase from Saccharomyces cerevisiae on thiosulfonate supports. in Journal of the Serbian Chemical Society. 2016;81(12):1371-1382.
doi:10.2298/JSC160730099M .
Mihailović, Mladen, Trbojević-Ivić, Jovana, Banjanac, Katarina, Milosavić, Nenad, Veličković, Dušan, Carević, Milica, Bezbradica, Dejan, "Immobilization of maltase from Saccharomyces cerevisiae on thiosulfonate supports" in Journal of the Serbian Chemical Society, 81, no. 12 (2016):1371-1382,
https://doi.org/10.2298/JSC160730099M . .
2
4
2

Proizvodnja sirovog ćelijskog ekstrakta beta-galaktozidaze pomoću bakterija mlečne kiseline

Carević, Milica; Stojanović, Marija; Jakovetić, Sonja; Mihailović, Mladen; Dimitrijević, Aleksandra; Trbojević, Jovana; Veličković, Dušan

(Beograd : Srpsko hemijsko društvo, 2012)

TY  - CONF
AU  - Carević, Milica
AU  - Stojanović, Marija
AU  - Jakovetić, Sonja
AU  - Mihailović, Mladen
AU  - Dimitrijević, Aleksandra
AU  - Trbojević, Jovana
AU  - Veličković, Dušan
PY  - 2012
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5330
PB  - Beograd : Srpsko hemijsko društvo
PB  - Belgrade : Serbian Chemical Society
C3  - Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.
T1  - Proizvodnja sirovog ćelijskog ekstrakta beta-galaktozidaze pomoću bakterija mlečne kiseline
SP  - 74
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5330
ER  - 
@conference{
author = "Carević, Milica and Stojanović, Marija and Jakovetić, Sonja and Mihailović, Mladen and Dimitrijević, Aleksandra and Trbojević, Jovana and Veličković, Dušan",
year = "2012",
publisher = "Beograd : Srpsko hemijsko društvo, Belgrade : Serbian Chemical Society",
journal = "Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.",
title = "Proizvodnja sirovog ćelijskog ekstrakta beta-galaktozidaze pomoću bakterija mlečne kiseline",
pages = "74",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5330"
}
Carević, M., Stojanović, M., Jakovetić, S., Mihailović, M., Dimitrijević, A., Trbojević, J.,& Veličković, D.. (2012). Proizvodnja sirovog ćelijskog ekstrakta beta-galaktozidaze pomoću bakterija mlečne kiseline. in Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.
Beograd : Srpsko hemijsko društvo., 74.
https://hdl.handle.net/21.15107/rcub_cherry_5330
Carević M, Stojanović M, Jakovetić S, Mihailović M, Dimitrijević A, Trbojević J, Veličković D. Proizvodnja sirovog ćelijskog ekstrakta beta-galaktozidaze pomoću bakterija mlečne kiseline. in Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.. 2012;:74.
https://hdl.handle.net/21.15107/rcub_cherry_5330 .
Carević, Milica, Stojanović, Marija, Jakovetić, Sonja, Mihailović, Mladen, Dimitrijević, Aleksandra, Trbojević, Jovana, Veličković, Dušan, "Proizvodnja sirovog ćelijskog ekstrakta beta-galaktozidaze pomoću bakterija mlečne kiseline" in Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012. (2012):74,
https://hdl.handle.net/21.15107/rcub_cherry_5330 .

Enzymatic synthesis of L-ascorbyl linoleate

Stojanović, Marija; Carević, Milica; Jakovetić, Sonja; Dimitrijević, Aleksandra; Trbojević, Jovana; Mihailović, Mladen; Veličković, Dušan

(2012)

TY  - CONF
AU  - Stojanović, Marija
AU  - Carević, Milica
AU  - Jakovetić, Sonja
AU  - Dimitrijević, Aleksandra
AU  - Trbojević, Jovana
AU  - Mihailović, Mladen
AU  - Veličković, Dušan
PY  - 2012
UR  - http://cherry.chem.bg.ac.rs/handle/123456789/5306
C3  - Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.
T1  - Enzymatic synthesis of L-ascorbyl linoleate
SP  - 64
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5306
ER  - 
@conference{
author = "Stojanović, Marija and Carević, Milica and Jakovetić, Sonja and Dimitrijević, Aleksandra and Trbojević, Jovana and Mihailović, Mladen and Veličković, Dušan",
year = "2012",
journal = "Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.",
title = "Enzymatic synthesis of L-ascorbyl linoleate",
pages = "64",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5306"
}
Stojanović, M., Carević, M., Jakovetić, S., Dimitrijević, A., Trbojević, J., Mihailović, M.,& Veličković, D.. (2012). Enzymatic synthesis of L-ascorbyl linoleate. in Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012., 64.
https://hdl.handle.net/21.15107/rcub_cherry_5306
Stojanović M, Carević M, Jakovetić S, Dimitrijević A, Trbojević J, Mihailović M, Veličković D. Enzymatic synthesis of L-ascorbyl linoleate. in Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012.. 2012;:64.
https://hdl.handle.net/21.15107/rcub_cherry_5306 .
Stojanović, Marija, Carević, Milica, Jakovetić, Sonja, Dimitrijević, Aleksandra, Trbojević, Jovana, Mihailović, Mladen, Veličković, Dušan, "Enzymatic synthesis of L-ascorbyl linoleate" in Prva konferencija mladih hemičara Srbije - Kratki izvodi radova, Beograd, 19. i 20. oktobar, 2012. (2012):64,
https://hdl.handle.net/21.15107/rcub_cherry_5306 .