Stanišić, Marija

Link to this page

Authority KeyName Variants
f216c01d-ebac-4b25-b73b-6065dafce08b
  • Stanišić, Marija (5)
  • Stanišić, Marija D. (2)
Projects

Author's Bibliography

Efficient enzyme@MOF composites for biocatalysis

Stanišić, Marija; Ristić, Predrag; Balaž, Ana Marija; Senćanski, Milan; Mitić, Dragana; Prodanović, Radivoje; Todorović, Tamara

(2022)


                                            

                                            
Stanišić, M., Ristić, P., Balaž, A. M., Senćanski, M., Mitić, D., Prodanović, R.,& Todorović, T.. (2022). Efficient enzyme@MOF composites for biocatalysis. in Book of abstracts - EUROBIOTECH 8th Central European Congress of Life Sciences, 20-22 June 2022, Krakow, Poland, 138-138.
https://hdl.handle.net/21.15107/rcub_cherry_5751
Stanišić M, Ristić P, Balaž AM, Senćanski M, Mitić D, Prodanović R, Todorović T. Efficient enzyme@MOF composites for biocatalysis. in Book of abstracts - EUROBIOTECH 8th Central European Congress of Life Sciences, 20-22 June 2022, Krakow, Poland. 2022;:138-138.
https://hdl.handle.net/21.15107/rcub_cherry_5751 .
Stanišić, Marija, Ristić, Predrag, Balaž, Ana Marija, Senćanski, Milan, Mitić, Dragana, Prodanović, Radivoje, Todorović, Tamara, "Efficient enzyme@MOF composites for biocatalysis" in Book of abstracts - EUROBIOTECH 8th Central European Congress of Life Sciences, 20-22 June 2022, Krakow, Poland (2022):138-138,
https://hdl.handle.net/21.15107/rcub_cherry_5751 .

The influence of isoenzymes composition and chemical modification on horseradish peroxidase@ZIF-8 bio-composite performance

Stanišić, Marija D.; Popović Kokar, Nikolina; Ristić, Predrag; Balaž, Ana Marija; Ognjanović, Miloš; Đokić, Veljko R.; Prodanović, Radivoje; Todorović, Tamara

(MDPI, 2022)

TY  - JOUR
AU  - Stanišić, Marija D.
AU  - Popović Kokar, Nikolina
AU  - Ristić, Predrag
AU  - Balaž, Ana Marija
AU  - Ognjanović, Miloš
AU  - Đokić, Veljko R.
AU  - Prodanović, Radivoje
AU  - Todorović, Tamara
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5561
AB  - Many articles in the literature deal with horseradish peroxidase (HRP) biomineralization,but none pay attention to the isoenzyme composition of commercial HRP or the influence of thecarbohydrate component of the protein molecule on the biomineralization process. To study theimpact of these factors, we performed periodate oxidation of commercial HRP and a purified HRP-Cisoform for biomineralization within ZIF-8. With purified HRP, enzyme@ZIF-8 biocomposites withhigher activity were obtained, while periodate oxidation of the carbohydrate component of bothcommercial HRP and purified HRP-C yields biocomposites with very high activity in acetate bufferthat does not degrade the ZIF-8 structure. Using acetate instead of phosphate buffer can prevent thefalse high activity of HRP@ZIF-8 biocomposites caused by the degradation of ZIF-8 coating. At thesame time, purification and especially oxidation of the carbohydrate component of enzymes prior tobiomineralization lead to significantly improved activity of the biocomposites.
PB  - MDPI
T2  - Polymers
T1  - The influence of isoenzymes composition and chemical modification on horseradish peroxidase@ZIF-8 bio-composite performance
VL  - 14
IS  - 22
SP  - 4834
DO  - 10.3390/polym14224834
ER  - 
@article{
author = "Stanišić, Marija D. and Popović Kokar, Nikolina and Ristić, Predrag and Balaž, Ana Marija and Ognjanović, Miloš and Đokić, Veljko R. and Prodanović, Radivoje and Todorović, Tamara",
year = "2022",
abstract = "Many articles in the literature deal with horseradish peroxidase (HRP) biomineralization,but none pay attention to the isoenzyme composition of commercial HRP or the influence of thecarbohydrate component of the protein molecule on the biomineralization process. To study theimpact of these factors, we performed periodate oxidation of commercial HRP and a purified HRP-Cisoform for biomineralization within ZIF-8. With purified HRP, enzyme@ZIF-8 biocomposites withhigher activity were obtained, while periodate oxidation of the carbohydrate component of bothcommercial HRP and purified HRP-C yields biocomposites with very high activity in acetate bufferthat does not degrade the ZIF-8 structure. Using acetate instead of phosphate buffer can prevent thefalse high activity of HRP@ZIF-8 biocomposites caused by the degradation of ZIF-8 coating. At thesame time, purification and especially oxidation of the carbohydrate component of enzymes prior tobiomineralization lead to significantly improved activity of the biocomposites.",
publisher = "MDPI",
journal = "Polymers",
title = "The influence of isoenzymes composition and chemical modification on horseradish peroxidase@ZIF-8 bio-composite performance",
volume = "14",
number = "22",
pages = "4834",
doi = "10.3390/polym14224834"
}
Stanišić, M. D., Popović Kokar, N., Ristić, P., Balaž, A. M., Ognjanović, M., Đokić, V. R., Prodanović, R.,& Todorović, T.. (2022). The influence of isoenzymes composition and chemical modification on horseradish peroxidase@ZIF-8 bio-composite performance. in Polymers
MDPI., 14(22), 4834.
https://doi.org/10.3390/polym14224834
Stanišić MD, Popović Kokar N, Ristić P, Balaž AM, Ognjanović M, Đokić VR, Prodanović R, Todorović T. The influence of isoenzymes composition and chemical modification on horseradish peroxidase@ZIF-8 bio-composite performance. in Polymers. 2022;14(22):4834.
doi:10.3390/polym14224834 .
Stanišić, Marija D., Popović Kokar, Nikolina, Ristić, Predrag, Balaž, Ana Marija, Ognjanović, Miloš, Đokić, Veljko R., Prodanović, Radivoje, Todorović, Tamara, "The influence of isoenzymes composition and chemical modification on horseradish peroxidase@ZIF-8 bio-composite performance" in Polymers, 14, no. 22 (2022):4834,
https://doi.org/10.3390/polym14224834 . .
4
1

Periodate oxidized glucose oxidase@ZIF-8 nanocomposite

Ristić, Predrag; Stanišić, Marija; Đokić, Veljko; Balaž, Ana Marija; Mitić, Dragana; Prodanović, Radivoje; Todorović, Tamara

(2022)

TY  - CONF
AU  - Ristić, Predrag
AU  - Stanišić, Marija
AU  - Đokić, Veljko
AU  - Balaž, Ana Marija
AU  - Mitić, Dragana
AU  - Prodanović, Radivoje
AU  - Todorović, Tamara
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5563
AB  - The durability of enzymes in harsh conditions can be enhanced by immobilization within metal-organic frameworks(MOFs) via a process called biomimetic mineralisation. Zeolitic imidazolate framework-8 (ZIF-8) is widely used as aprotective coating to encapsulate proteins. The formation of nucleation centres and further biocomposite particlegrowth is entirely governed by the pure electrostatic interactions between the protein’s surface and positively chargedZn(II) metal ions. It was previously shown that enhancing these electrostatic interactions by a chemical modificationof surface amino acid residues can lead to a rapid biocomposite formation. However, a chemical modification ofcarbohydrate components by periodate oxidation for glycoproteins can serve as an alternative strategy. In the presentstudy, an industrially important enzyme glucose oxidase (GOx) was selected as a model system. Periodate oxidationof GOx by 2.5 mM sodium periodate increased negative charge on the enzyme molecule. Biomineralizationexperiments with oxidized GOx resulted in higher specific activity, effectiveness factor, and higher thermostability ofthe ZIF-8 biocomposites.
C3  - Book of abstracts - NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece
T1  - Periodate oxidized glucose oxidase@ZIF-8 nanocomposite
SP  - 138
EP  - 138
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5753
ER  - 
@conference{
author = "Ristić, Predrag and Stanišić, Marija and Đokić, Veljko and Balaž, Ana Marija and Mitić, Dragana and Prodanović, Radivoje and Todorović, Tamara",
year = "2022",
abstract = "The durability of enzymes in harsh conditions can be enhanced by immobilization within metal-organic frameworks(MOFs) via a process called biomimetic mineralisation. Zeolitic imidazolate framework-8 (ZIF-8) is widely used as aprotective coating to encapsulate proteins. The formation of nucleation centres and further biocomposite particlegrowth is entirely governed by the pure electrostatic interactions between the protein’s surface and positively chargedZn(II) metal ions. It was previously shown that enhancing these electrostatic interactions by a chemical modificationof surface amino acid residues can lead to a rapid biocomposite formation. However, a chemical modification ofcarbohydrate components by periodate oxidation for glycoproteins can serve as an alternative strategy. In the presentstudy, an industrially important enzyme glucose oxidase (GOx) was selected as a model system. Periodate oxidationof GOx by 2.5 mM sodium periodate increased negative charge on the enzyme molecule. Biomineralizationexperiments with oxidized GOx resulted in higher specific activity, effectiveness factor, and higher thermostability ofthe ZIF-8 biocomposites.",
journal = "Book of abstracts - NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece",
title = "Periodate oxidized glucose oxidase@ZIF-8 nanocomposite",
pages = "138-138",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5753"
}
Ristić, P., Stanišić, M., Đokić, V., Balaž, A. M., Mitić, D., Prodanović, R.,& Todorović, T.. (2022). Periodate oxidized glucose oxidase@ZIF-8 nanocomposite. in Book of abstracts - NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece, 138-138.
https://hdl.handle.net/21.15107/rcub_cherry_5753
Ristić P, Stanišić M, Đokić V, Balaž AM, Mitić D, Prodanović R, Todorović T. Periodate oxidized glucose oxidase@ZIF-8 nanocomposite. in Book of abstracts - NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece. 2022;:138-138.
https://hdl.handle.net/21.15107/rcub_cherry_5753 .
Ristić, Predrag, Stanišić, Marija, Đokić, Veljko, Balaž, Ana Marija, Mitić, Dragana, Prodanović, Radivoje, Todorović, Tamara, "Periodate oxidized glucose oxidase@ZIF-8 nanocomposite" in Book of abstracts - NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece (2022):138-138,
https://hdl.handle.net/21.15107/rcub_cherry_5753 .

Periodate oxidized horseradish peroxidase@ZIF-8 nanocomposite

Stanišić, Marija; Ristić, Predrag; Đokić, Veljko; Balaž, Ana Marija; Prodanović, Radivoje; Todorović, Tamara

(2022)

TY  - CONF
AU  - Stanišić, Marija
AU  - Ristić, Predrag
AU  - Đokić, Veljko
AU  - Balaž, Ana Marija
AU  - Prodanović, Radivoje
AU  - Todorović, Tamara
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5562
AB  - Metal-organic frameworks (MOFs) are a class of materials well-known for their high degree of crystallinity andultrahigh porosity. Modular synthesis from organic linkers and metal nodes allows for precise control of structure,pore size and chemical functionality of MOFs. Recently, MOFs have been explored for their potential to form novelbiocomposites with proteins by a process termed biomimetic mineralization. These novel MOF biocomposites showgreat promise for application to industrial biocatalysis where strategies for enhancing enzyme stability are ofsignificant interest. The protective capacity and applications of biomimetically mineralized biomacromolecule zeoliticimidazolate framework (ZIF-8) composites are likely dependent on the charge of the biomolecule and the topologyof the mineralized ZIF-8 coating. Herein, we identify conditions to reliably yield the porous periodate oxidizedhorseradish peroxidase@ZIF-8 sodalite topology biocomposite in preference to other more dense phases.
C3  - NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece
T1  - Periodate oxidized horseradish peroxidase@ZIF-8 nanocomposite
SP  - 138
EP  - 138
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5752
ER  - 
@conference{
author = "Stanišić, Marija and Ristić, Predrag and Đokić, Veljko and Balaž, Ana Marija and Prodanović, Radivoje and Todorović, Tamara",
year = "2022",
abstract = "Metal-organic frameworks (MOFs) are a class of materials well-known for their high degree of crystallinity andultrahigh porosity. Modular synthesis from organic linkers and metal nodes allows for precise control of structure,pore size and chemical functionality of MOFs. Recently, MOFs have been explored for their potential to form novelbiocomposites with proteins by a process termed biomimetic mineralization. These novel MOF biocomposites showgreat promise for application to industrial biocatalysis where strategies for enhancing enzyme stability are ofsignificant interest. The protective capacity and applications of biomimetically mineralized biomacromolecule zeoliticimidazolate framework (ZIF-8) composites are likely dependent on the charge of the biomolecule and the topologyof the mineralized ZIF-8 coating. Herein, we identify conditions to reliably yield the porous periodate oxidizedhorseradish peroxidase@ZIF-8 sodalite topology biocomposite in preference to other more dense phases.",
journal = "NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece",
title = "Periodate oxidized horseradish peroxidase@ZIF-8 nanocomposite",
pages = "138-138",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5752"
}
Stanišić, M., Ristić, P., Đokić, V., Balaž, A. M., Prodanović, R.,& Todorović, T.. (2022). Periodate oxidized horseradish peroxidase@ZIF-8 nanocomposite. in NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece, 138-138.
https://hdl.handle.net/21.15107/rcub_cherry_5752
Stanišić M, Ristić P, Đokić V, Balaž AM, Prodanović R, Todorović T. Periodate oxidized horseradish peroxidase@ZIF-8 nanocomposite. in NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece. 2022;:138-138.
https://hdl.handle.net/21.15107/rcub_cherry_5752 .
Stanišić, Marija, Ristić, Predrag, Đokić, Veljko, Balaž, Ana Marija, Prodanović, Radivoje, Todorović, Tamara, "Periodate oxidized horseradish peroxidase@ZIF-8 nanocomposite" in NANOTEXNOLOGY NN22, 19th International Conference on Nanosciences & Nanotechnologies, 5-8 July 2022, Thessaloniki, Greece (2022):138-138,
https://hdl.handle.net/21.15107/rcub_cherry_5752 .

Chemical modification of glycoproteins’ carbohydrate moiety as a general strategy for the synthesis of efficient biocatalysts by biomimetic mineralization: The case of glucose oxidase

Stanišić, Marija D.; Popović Kokar, Nikolina; Ristić, Predrag; Balaž, Ana Marija; Senćanski, Milan; Ognanović, Miloš; Đokić, Veljko R.; Prodanović, Radivoje; Todorović, Tamara

(MDPI, 2021)

TY  - JOUR
AU  - Stanišić, Marija D.
AU  - Popović Kokar, Nikolina
AU  - Ristić, Predrag
AU  - Balaž, Ana Marija
AU  - Senćanski, Milan
AU  - Ognanović, Miloš
AU  - Đokić, Veljko R.
AU  - Prodanović, Radivoje
AU  - Todorović, Tamara
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4895
AB  - Zeolitic imidazolate framework-8 (ZIF-8) is widely used as a protective coating to en-capsulate proteins via biomimetic mineralization. The formation of nucleation centers and further biocomposite crystal growth is entirely governed by the pure electrostatic interactions between the protein’s surface and the positively charged Zn(II) metal ions. It was previously shown that enhancing these electrostatic interactions by a chemical modification of surface amino acid residues can lead to a rapid biocomposite crystal formation. However, a chemical modification of carbohydrate components by periodate oxidation for glycoproteins can serve as an alternative strategy. In the present study, an industrially important enzyme glucose oxidase (GOx) was selected as a model system. Periodate oxidation of GOx by 2.5 mM sodium periodate increased negative charge on the enzyme molecule, from −10.2 to −36.9 mV, as shown by zeta potential measurements and native PAGE electrophoresis. Biomineralization experiments with oxidized GOx resulted in higher specific activity, effectiveness factor, and higher thermostability of the ZIF-8 biocomposites. Periodate oxidation of carbohydrate components for glycoproteins can serve as a facile and general method for facilitating the biomimetic mineralization of other industrially relevant glycoproteins.
PB  - MDPI
T2  - Polymers
T1  - Chemical modification of glycoproteins’ carbohydrate moiety as a general strategy for the synthesis of efficient biocatalysts by biomimetic mineralization: The case of glucose oxidase
VL  - 13
IS  - 22
SP  - 2
EP  - 12
DO  - 10.3390/polym13223875
ER  - 
@article{
author = "Stanišić, Marija D. and Popović Kokar, Nikolina and Ristić, Predrag and Balaž, Ana Marija and Senćanski, Milan and Ognanović, Miloš and Đokić, Veljko R. and Prodanović, Radivoje and Todorović, Tamara",
year = "2021",
abstract = "Zeolitic imidazolate framework-8 (ZIF-8) is widely used as a protective coating to en-capsulate proteins via biomimetic mineralization. The formation of nucleation centers and further biocomposite crystal growth is entirely governed by the pure electrostatic interactions between the protein’s surface and the positively charged Zn(II) metal ions. It was previously shown that enhancing these electrostatic interactions by a chemical modification of surface amino acid residues can lead to a rapid biocomposite crystal formation. However, a chemical modification of carbohydrate components by periodate oxidation for glycoproteins can serve as an alternative strategy. In the present study, an industrially important enzyme glucose oxidase (GOx) was selected as a model system. Periodate oxidation of GOx by 2.5 mM sodium periodate increased negative charge on the enzyme molecule, from −10.2 to −36.9 mV, as shown by zeta potential measurements and native PAGE electrophoresis. Biomineralization experiments with oxidized GOx resulted in higher specific activity, effectiveness factor, and higher thermostability of the ZIF-8 biocomposites. Periodate oxidation of carbohydrate components for glycoproteins can serve as a facile and general method for facilitating the biomimetic mineralization of other industrially relevant glycoproteins.",
publisher = "MDPI",
journal = "Polymers",
title = "Chemical modification of glycoproteins’ carbohydrate moiety as a general strategy for the synthesis of efficient biocatalysts by biomimetic mineralization: The case of glucose oxidase",
volume = "13",
number = "22",
pages = "2-12",
doi = "10.3390/polym13223875"
}
Stanišić, M. D., Popović Kokar, N., Ristić, P., Balaž, A. M., Senćanski, M., Ognanović, M., Đokić, V. R., Prodanović, R.,& Todorović, T.. (2021). Chemical modification of glycoproteins’ carbohydrate moiety as a general strategy for the synthesis of efficient biocatalysts by biomimetic mineralization: The case of glucose oxidase. in Polymers
MDPI., 13(22), 2-12.
https://doi.org/10.3390/polym13223875
Stanišić MD, Popović Kokar N, Ristić P, Balaž AM, Senćanski M, Ognanović M, Đokić VR, Prodanović R, Todorović T. Chemical modification of glycoproteins’ carbohydrate moiety as a general strategy for the synthesis of efficient biocatalysts by biomimetic mineralization: The case of glucose oxidase. in Polymers. 2021;13(22):2-12.
doi:10.3390/polym13223875 .
Stanišić, Marija D., Popović Kokar, Nikolina, Ristić, Predrag, Balaž, Ana Marija, Senćanski, Milan, Ognanović, Miloš, Đokić, Veljko R., Prodanović, Radivoje, Todorović, Tamara, "Chemical modification of glycoproteins’ carbohydrate moiety as a general strategy for the synthesis of efficient biocatalysts by biomimetic mineralization: The case of glucose oxidase" in Polymers, 13, no. 22 (2021):2-12,
https://doi.org/10.3390/polym13223875 . .
1
3
2

Biomimetic mineralisation of periodate oxidized glucose oxidase

Stanišić, Marija; Popović, Nikolina; Ristić, Predrag; Balaž, Ana Marija; Senćanski, Milan; Prodanović, Radivoje; Todorović, Tamara

(Beograd : Biohemijsko društvo Srbije, 2021)

TY  - CONF
AU  - Stanišić, Marija
AU  - Popović, Nikolina
AU  - Ristić, Predrag
AU  - Balaž, Ana Marija
AU  - Senćanski, Milan
AU  - Prodanović, Radivoje
AU  - Todorović, Tamara
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5564
AB  - Glucose oxidase (GOx) is an enzyme that belongs to a group of oxidoreductases. This enzyme catalyzes the oxidation of glucose to gluconic acid using molecular oxygen as an electron acceptor. Glucose oxidase contains carbohydrates in its structure, most often mannose and glucose (11-13%) 1. Durability of GOx in harsh conditions can be enhanced by encapsulation within metal–organic frameworks via a process called biomimetic mineralisation. We demonstrate that chemical modification of carbohydrate parts on the protein surface by periodate oxidation is an effective method for control of biomimetic mineralisation by zeolitic imidazolate framework-8 (ZIF-8). Obtained GOx-ZIF-8 biocomposite had the higher half-life at 65oC, and higher specific activity than native GOx.
PB  - Beograd : Biohemijsko društvo Srbije
C3  - Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac, Book of Abstracts
T1  - Biomimetic mineralisation of periodate oxidized glucose oxidase
SP  - 148
EP  - 148
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5748
ER  - 
@conference{
author = "Stanišić, Marija and Popović, Nikolina and Ristić, Predrag and Balaž, Ana Marija and Senćanski, Milan and Prodanović, Radivoje and Todorović, Tamara",
year = "2021",
abstract = "Glucose oxidase (GOx) is an enzyme that belongs to a group of oxidoreductases. This enzyme catalyzes the oxidation of glucose to gluconic acid using molecular oxygen as an electron acceptor. Glucose oxidase contains carbohydrates in its structure, most often mannose and glucose (11-13%) 1. Durability of GOx in harsh conditions can be enhanced by encapsulation within metal–organic frameworks via a process called biomimetic mineralisation. We demonstrate that chemical modification of carbohydrate parts on the protein surface by periodate oxidation is an effective method for control of biomimetic mineralisation by zeolitic imidazolate framework-8 (ZIF-8). Obtained GOx-ZIF-8 biocomposite had the higher half-life at 65oC, and higher specific activity than native GOx.",
publisher = "Beograd : Biohemijsko društvo Srbije",
journal = "Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac, Book of Abstracts",
title = "Biomimetic mineralisation of periodate oxidized glucose oxidase",
pages = "148-148",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5748"
}
Stanišić, M., Popović, N., Ristić, P., Balaž, A. M., Senćanski, M., Prodanović, R.,& Todorović, T.. (2021). Biomimetic mineralisation of periodate oxidized glucose oxidase. in Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac, Book of Abstracts
Beograd : Biohemijsko društvo Srbije., 148-148.
https://hdl.handle.net/21.15107/rcub_cherry_5748
Stanišić M, Popović N, Ristić P, Balaž AM, Senćanski M, Prodanović R, Todorović T. Biomimetic mineralisation of periodate oxidized glucose oxidase. in Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac, Book of Abstracts. 2021;:148-148.
https://hdl.handle.net/21.15107/rcub_cherry_5748 .
Stanišić, Marija, Popović, Nikolina, Ristić, Predrag, Balaž, Ana Marija, Senćanski, Milan, Prodanović, Radivoje, Todorović, Tamara, "Biomimetic mineralisation of periodate oxidized glucose oxidase" in Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac, Book of Abstracts (2021):148-148,
https://hdl.handle.net/21.15107/rcub_cherry_5748 .

Horseradish peroxidase C1A wild type gene and its variants expressed in Pichia pastoris KM71H strain

Balaž, Ana Marija; Crnoglavac Popović, Milica; Stanišić, Marija; Ristić, Predrag; Senćanski, Milan; Todorović, Tamara; Prodanović, Radivoje

(2021)

TY  - CONF
AU  - Balaž, Ana Marija
AU  - Crnoglavac Popović, Milica
AU  - Stanišić, Marija
AU  - Ristić, Predrag
AU  - Senćanski, Milan
AU  - Todorović, Tamara
AU  - Prodanović, Radivoje
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5566
AB  - Enzyme immobilization enables maintenance of enzyme activity and structural stability even in adverse conditions 1. Structural changes in enzymes that can occur due to the action of organic solvents, inhibitors or increased temperature can be prevented by immobilization of the enzymes in metal–organic frameworks (MOFs). It is reported that several enzymes, such as cytochrome c and horseradish peroxidase (HRP) have been successfully incorporated into MOFs 2. The aim of this work is to produce wild type horseradish peroxidase, isoform C1A, and several mutants specially designed to increase the activity and stability of HRP while immobilized within selected MOFs. Wild type and its variants were produced in metalotrophic yeast, Pichia pastoris KM71H strain, their activity and basic kinetic parameters were determined and compared prior imobilization.
C3  - Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac
T1  - Horseradish peroxidase C1A wild type gene and its variants expressed in Pichia pastoris KM71H strain
SP  - 49
EP  - 49
UR  - https://hdl.handle.net/21.15107/rcub_cherry_5747
ER  - 
@conference{
author = "Balaž, Ana Marija and Crnoglavac Popović, Milica and Stanišić, Marija and Ristić, Predrag and Senćanski, Milan and Todorović, Tamara and Prodanović, Radivoje",
year = "2021",
abstract = "Enzyme immobilization enables maintenance of enzyme activity and structural stability even in adverse conditions 1. Structural changes in enzymes that can occur due to the action of organic solvents, inhibitors or increased temperature can be prevented by immobilization of the enzymes in metal–organic frameworks (MOFs). It is reported that several enzymes, such as cytochrome c and horseradish peroxidase (HRP) have been successfully incorporated into MOFs 2. The aim of this work is to produce wild type horseradish peroxidase, isoform C1A, and several mutants specially designed to increase the activity and stability of HRP while immobilized within selected MOFs. Wild type and its variants were produced in metalotrophic yeast, Pichia pastoris KM71H strain, their activity and basic kinetic parameters were determined and compared prior imobilization.",
journal = "Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac",
title = "Horseradish peroxidase C1A wild type gene and its variants expressed in Pichia pastoris KM71H strain",
pages = "49-49",
url = "https://hdl.handle.net/21.15107/rcub_cherry_5747"
}
Balaž, A. M., Crnoglavac Popović, M., Stanišić, M., Ristić, P., Senćanski, M., Todorović, T.,& Prodanović, R.. (2021). Horseradish peroxidase C1A wild type gene and its variants expressed in Pichia pastoris KM71H strain. in Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac, 49-49.
https://hdl.handle.net/21.15107/rcub_cherry_5747
Balaž AM, Crnoglavac Popović M, Stanišić M, Ristić P, Senćanski M, Todorović T, Prodanović R. Horseradish peroxidase C1A wild type gene and its variants expressed in Pichia pastoris KM71H strain. in Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac. 2021;:49-49.
https://hdl.handle.net/21.15107/rcub_cherry_5747 .
Balaž, Ana Marija, Crnoglavac Popović, Milica, Stanišić, Marija, Ristić, Predrag, Senćanski, Milan, Todorović, Tamara, Prodanović, Radivoje, "Horseradish peroxidase C1A wild type gene and its variants expressed in Pichia pastoris KM71H strain" in Tenth Conference of Serbian Biochemical Society, 24 September 2021, Kragujevac (2021):49-49,
https://hdl.handle.net/21.15107/rcub_cherry_5747 .