Optimization of Crude Protease Production from Bacillus thuringiensis HSFI-12 and Thrombolytic Activity Its Enzyme Dialysate
DOI:
https://doi.org/10.48048/tis.2022.1952Keywords:
Bacillus thuringiensis, Cardiovascular disease, Thrombolytic agent, Protease activity, Molecular identificationAbstract
Cardiovascular disease (CVD) is among the leading causes of death in the world caused by thrombosis. Thrombosis is the formation of excessive blood clots on the walls of blood vessels called thrombus. This could lead to fatal blockage of the heart muscle or brain. Thrombosis can be treated using enzyme-type drugs such as thrombolytic proteases. There have been many studies of bacteria producing thrombolytic enzymes isolated from fermented foodstuffs. However, commercial production of bacterial enzymes to fulfill the need of thrombolytic agents is still limited, causing high price of CVD therapy. Bacillus sp. HSFI-12 (Holothuria scabra Fermented Intestine-12) isolated from the fermented intestine of sea cucumber Holothuria scabra had been reported to have a competitive thrombolytic activity to the commercial Nattokinase. This study aimed to determine bacterial optimum incubation time based on enzyme activity after bacterium molecular identification was done. It also aimed to obtain the dialysate of bacterial crude protease and then determine the thrombolytic activity of the obtained dialysate. Thrombolytic activity was tested on 4 different types of blood (A, B, AB and O). Results of molecular identification showed that strain HSFI-12 shared similarity level of 99.80 %, with Bacillus thuringiensis. Activity of crude protease from the incubated cultures peaked at 48 h of incubation with activity of 191.5 U/mL The activity of concentrated protease after precipitation and dialysis process (dialysate) was 2-times higher by 355,7 U/mL. The percentage of lysis of blood clots produced by crude blood groups A, B, AB and O showed a range of values of 66.423 - 67.656 % while those that produce dialysate are 77.564 - 78.861 %. As conclusion, the best (optimized) incubation time to produce crude enzyme from B. thuringiensis HSFI-12 with the highest activity was 48 h. The process of concentrating the crude thrombolytic protease of B. thuringiensis HSFI-12 increases both activity and thrombolytic ability of the bacterial enzyme.
HIGHLIGHTS
- The most optimum incubation time for protease production from Bacillus thuringiensis is 48 h
- Partial purification on bacterial crude protease through resulted in 86 % increased activity
- Partial purification on bacterial crude protease resulted in 17 % increased blood clot lysis ability
- Clot lysis ability of both crude and dialysate proteases are higher than that of Nattokinase (NK)
GRAPHICAL ABSTRACT 
Downloads
References
L Aryan, D Younessi, M Zargari, S Banerjee, J Agopian, S Rahman, R Borna, G Ruffenach, S Umar and M Eghbali. The role of estrogen receptors in cardiovascular disease. Int. J. Mol. Sci. 2020; 21, 4314.
World Health Organization. Cardiovascular diseases, Available at: https://www.who.int/en/news-room/fact-sheets/detail/cardiovascular-diseases-(cvds), accessed January 2022.
Riskesdas (Riset Kesehatan Dasar, Basic Health Research), Available at: https://kesmas.kemkes.go. id/assets/upload/dir_519d41d8cd98f00/files/Hasil-riskesdas-2018_1274.pdf, accessed January 2022.
V Kartal, Z Zara, S Yilmaz, A Ayhan, A Yoruk and C Timur. A thrombosis story and PRES. North. Clin. Istanb. 2014; 1, 49-52.
SJ Martina, LAP Ramar, MRI Silaban, M Luthfi and PAP Govin. Antiplatelet effectivity between aspirin with honey on cardiovascular disease based on bleeding time taken on mice. Open Access Maced J. Med. Sci. 2019; 7, 3416-20.
M Kumar, K Seema, A Prasad, AK Sharma and BL Sherwal. Molecular confirmation of the circulating Bacillus anthracis during outbreak of anthrax in different villages of Simdega District, Jharkhand. Indian J. Med. Microbiol. 2019; 37, 116-9.
T Akhtar, M Hoq and A Mazid. Bacterial proteases as thrombolytics and fibrinolytics. Dhaka Univ. J. Pharm. Sci. 2017; 16, 255-69.
C Sharma, GEM Salem, N Sharma, P Gautam and R Singh. Thrombolytic potential of novel thiol-dependent fibrinolytic protease from Bacillus cereus RSA1. Biomolecules 2019; 10, 3.
F Paciullo, L Bury, P Noris, E Falcinelli, F Melazzini, S Orsini, C Zaninetti, R Abdul-Kadir, D Screwdriver-Tuudah, PG Heller, AC Glembotsky, F Fabris, J Rivera, ML Lozano, N Butta, R Favier, AR Cid, M Fouassier, GM Podda, C Santoro, E Grandone, Y Henskens, P Nurden, B Zieger, A Cuker, K Devreese, A Tosetto, E De Candia, A Dupuis, K Miyazaki, M Othman and P Gresele. Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT Study. Haematologica 2020; 105, 1948-56.
D Swan, N Loughran, M Makris and J Thachil. Management of bleeding and procedures in patients on antiplatelet therapy. Blood Rev. 2020; 39, 100619.
Y Devaraj, SK Rajender and PM Halami. Purification and characterization of fibrinolytic protease from Bacillus amyloliquefaciens MCC2606 and analysis of fibrin degradation product by MS/MS. Prep. Biochem. Biotechnol. 2018; 48, 172-80.
D Dhamodharan, SN Jemimah, KS Merlyn and DC Subathra. Novel fibrinolytic protease producing Streptomyces radiopugnans VITSD8 from marine sponges. Mar. Drugs 2019; 17, 164.
N Hidayati, H Fuad, H Munandar, DS Zilda, N Nurrahman, M Fattah, O Oedjijono, A Samiasih and SN Ethica. Proteolytic and clot lysis activity screening of crude proteases extracted from tissues and bacterial isolates of Holothuria Scabra. IOP Conf. Ser.: Earth Environ. Sci. 2021; 755, 012016.
S Mohamadi, M Mehrabi and S Sajadimajd. Purification and characterization of an extracellular alkaline solvent-stable metalloprotease secreted from newly isolated Bacillus sp. DEM05: Optimization of protease production. Iran. J. Biotechnol. 2021; 19, e2866.
N Niederstebruch and D Sixt. Standard nutrient agar 1 as a substitute for blood-supplemented Müller-Hinton agar for antibiograms in developing countries. Eur. J. Clin. Microbiol. Infect. Dis. 2013; 32, 237-41.
N Hidayati, N Nurrahman, H Fuad, H Munandar, DS Zilda, AR Ernanto, A Samiasih, O Oedjijono and SN Ethica. Bacillus tequilensis isolated from fermented intestine of Holothuria scabra produces fibrinolytic protease with thrombolysis activity. IOP Conf. Ser. Earth Environ. Sci. 2021; 707, 012008.
DA Lestari, SI Muchlissin, AH Mukaromah, S Darmawati and SN Ethica. Isolation of protease-producing bacteria Bacillus megaterium IROD3 from red oncom after 72 h fermentation (in Indonesian). In: Proceedings of the Seminar Nasional Pendidikan Sains dan Teknologi, Semarang, Indonesia. 2018, p. 31-9.
B Gao, X Shang, L Li, W Di and R Zeng. Phylogenetically diverse, acetaldehyde-degrading bacterial community in the deep-sea water of the West Pacific Ocean. Acta Oceanol. Sin. 2018; 37, 54-64.
C Delbès, L Ali-Mandjee and MC Montel. Monitoring bacterial communities in raw milk and cheese by culture-dependent and-independent 16S rRNA gene-based analyses. Appl. Environ. Microbiol. 2007; 73, 1882-91.
HA Azali, V Maillot, N Cassam, T Chesneau, J Soulezelle, S Scussel, ALA Karime, B Hostachy, B Reynaud, M Roux-Cuvelier and I Robène. Occurrence of cassava brown streak disease and associated Cassava brown streak virus and Ugandan cassava brown streak virus in the Comoros Islands. New Dis. Rep. 2017; 36, 19.
T Madden. The BLAST sequence analysis tool. In: The NCBI handbook. National Center for Biotechnology Information, Bethesda, Maryland, 2013, p. 425-36.
AU Iskandar, SN Ethica, A Sukeksi, AH Mukaromah, AR Sulistyaningtyas and S Darmawati. Molecular systematic and phylogenetic analysis of indigenous bacterial isolates with potential as bioremediation agent based on 16S rRNA gene analysis. In: Proceedings of the 11th International Conference on Global Resource Conservation, East Java, Indonesia. 2021, p. 012010.
H Fuad, N Hidayati, S Darmawati, H Munandar, AR Sulistyaningtyas, N Nurrahman, AR Ernanto, DS Zilda, W Widjanarka and NE Stalis. Prospects of fibrinolytic proteases of bacteria from sea cucumber fermentation products as antithrombotic agent. In: Proceedings of the 3rd International Conference on Bioinformatics, Biotechnology, and Biomedical Engineering, Yogyakarta, Indonesia. 2020.
DS Zilda, E Harmayani, J Widada, W Asmara, HE Irianto, G Patantis and YN Fawzya. Screening of thermostable protease producing microorganisms isolated from Indonesian hotspring. Squalen Bull. Mar. Fish. Postharvest Biotech. 2012; 7, 105-14.
DS Zilda, YN Fawzya and AR Uria. Identification of protease-producing bacteria isolated from Banyuwedang, Bali, and characterization of its protease. Squalen Bull. Mar. Fish. Postharvest Biotech. 2018; 13, 101-8.
S Farooq, R Nazir, SA Ganai and BA Ganai. Isolation and characterization of a new cold-active protease from psychrotrophic bacteria of Western Himalayan glacial soil. Sci. Rep. 2021; 11, 12768.
HU Bergmeyer. Methods of enzymatic analysis: Metabolites 1: Carbohydrates. Verlag Chemie, 1984, p. 649.
AK Wardani and LO Nindita. Purification and characterization of proteases from bacteria produced isolation from Whey tofu. J. Agric. Technol. 2012; 13, 149-56.
S Prasad, RS Kashyap, JY Deopujari, HJ Purohit, GM Taori and HF Daginawala. Development of an in vitro model to study clot lysis activity of thrombolytic drugs. Thromb. J. 2006; 4, 14.
R Rusyiana, IA Lestarini, CD Hamdin and H Muliasari. Anticoagulant activity of mangrove (Avicennia alba) leaves extract in vitro. Indones. J. Mar. Sci. 2021; 26, 110-6.
RA Tangkery, DS Paransa and A Rumengan. Anticoagulant activity test of mangrove Aegiceras corniculatum extract. J. Coast. Trop. Oceans 2013; 1, 7-14.
SN Ethica and TJ Raharjo. 2014, Detection of genes involved in glycerol metabolism of Alcaligenes sp. JG3. Ph.D. Thesis, Universitas Gadjah Mada, Yogyakarta, Indonesia.
J Sambrook, ER Fritsch and T Maniatis. Molecular cloning: A laboratory manual. Cold Spring Harbor Laboratory Press, New York, 1989.
MR Green and J Sambrook. Cloning and transformation with plasmid vectors. Cold Spring Harbor Protoc. 2021. https://doi.org/10.1101/pdb.top101170
SN Ethica and A Sabdono. Phylogenetic analysis and screening of hydrolytic bacteria with hydrolase enzyme activity from hospital wastewater of Semarang, Central Java, Indonesia. Ecol. Eng. Environ. Technol. 2021; 22, 81-6.
R Perwendha, A Oetari and W Sjamsuridzal. Skimmed milk-degrading ability of Rhizopus azygosporus UICC 539 at various temperatures. AIP Conf. Proc. 2020; 2242, 050006.
S Raut, SK Sen, NA Kabir, S Satpathy and S Raut. Isolation and characterization of protease producing bacteria from upper respiratory tract of wild chicken. Bioinformation 2012; 8, 326-30.
A Baehaki and A Budiman. Isolation and characterization of proteases from bacteria from the Indralaya swamp soil, South Sumatra (in Indonesian). J. Food Technol. Ind. 2011; 22, 37-42.
RR Burgess. Protein precipitation techniques. Meth. Enzymol. 2009; 463, 331-42.
PB Sridhara, C Dharmashekara, C Srinivasa, C Shivamallu, SP Kollur, SM Gopinath, A Syed, SS Patil, A Prasad and DE Salamun. Isolation, characterization, and optimization of protease producing bacterium Bacillus thuringiensis from paddy field soil. Pharmacogn. Res. 2021; 13, 89-95.
SL Harer, MS Bhatia and NM Bhatia. Isolation, purification and partial characterization of thermostable serine alkaline protease from a newly isolated Bacillus thuringinsis-SH-II-1A. Afr. J. Biotechnol. 2018; 17, 178-88.
R Hadjidj, A Badis, S Mechri, K Eddouaouda, L Khelouia, R Annane, ME Hattab and B Jaouadi. Purification, biochemical, and molecular characterization of novel protease from Bacillus licheniformis strain K7A. Int. J. Biol. Macromol. 2018; 114, 1033-48.
JY Jang, TS Kim, J Cai, J Kim, Y Kim, K Shin, KS Kim, SK Park, SP Lee, EK Choi, MH Rhee and YB Kim. Nattokinase improves blood flow by inhibiting platelet aggregation and thrombus formation. Lab. Anim. Res. 2013; 29, 221-5.
Downloads
Published
Issue
Section
License
Copyright (c) 2022 Walailak University

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.



