Enhanced production of nattokinase from UV mutated Bacillus sp.
Abstract
In the recent years, nattokinase is one of the most-often employed among the several thrombolytic agents used clinically, particularly because of its lower cost comparing to other thrombolytic agents. In the present research work, Bacillus sp. was isolated from the heterogeneous microbial population present in the soil sample and screened for the production of nattokinase. The production of the enzyme was carried out using two different media (with and without shrimp shell substrate). Nattokinase activity (clot buster) was determined by using a modified Holmstorm method. The production strain SFN01 was improved by random mutagenesis (UV radiation) and the enzyme activity was checked with the enzyme produced by wild strain. The mutated strains had exhibited a higher clot lysis activity in which 1 unit of the enzyme completely lyses 1 mL of human blood when compared to the wild strain. Nattokinase produced by SFN showed a retention time of 10.6 min in RP-HPLC chromatogram.
Introduction
Myocardial infarction is the most common contributor of morbidity and mortality worldwide. Stroke is the third leading cause of death. According to World Health Organization, nearly 8 million people worldwide suffer from myocardial infarction and in India approximately 2.5 crores of people exist. In India, 31.7% of deaths occur due to MI. Incidence of cardiovascular disease was about 7% in 1970 and increased up to 32% in 2011 in India (Reddy, 2007). Enzyme therapies are becoming more prevalent in medicine today, with many manufacturers targeting their advantages in disease treatment. In the last 100 years, enzymes have been increasingly used to treat various cardiovascular diseases. Nature has designed a system the body uses to maintain and repair itself. When the vascular system is injured the body responds quickly to stop the bleeding and repair the damage. Circulating platelets are called into action to quickly seal the leak by forming a blood clot. Not all blood clot is desirable. Thrombosis is an abnormal blood clot inside a blood vessel. The blood clots can detach from the vascular wall and travel in the blood. These free floating thrombi (now called emboli) can lodge anywhere in the cardiovascular system, including the lungs or brain (as in a thrombotic stroke). It is fibrin that is implicated in many heart attacks, since cardiac arrest usually occurs after a plaque's cap fractures, causing a blood clot to form over the fracture and block blood flow. Nattokinase is an ideal treatment, therefore, for heart attack patients, ischemic stroke patients, and for those who are at risk of pulmonary embolism or deep vein thrombosis-in short, and for any patient with a clotting problem.
The major thrombolytic agents are classified into two types. The first one is the plasminogen activators, such as urokinase, and the second one is tissue type plasminogen activator (tPA), streptokinase, and both activate plasminogen to plasmin, and the plasmin like proteins, such as nattokinase and lumbrikinase, which can directly degrade the fibrin. The enzyme nattokinase offers a completely natural means of helping to prevent and dissolve blood clots. It closely resembles plasmin.
So far, many researchers have focused their efforts on the isolating and screening of microorganisms for enzyme production with high fibrinolytic activity (Chang et al., 2000), as well as on the purifying and characterizing of newly found enzyme (Kim et al., 1996). Evidences suggest that B. subtilis secrete nattokinase. NK is primarily found from a traditional fermented soybean food named as "Natto" in Japan (Sumi et al., 1987). It is a subtilisin-like serine protease with molecular weight of 27,000-42,000 Da (Chang et al., 2000; Fujita et al., 1993; Kim et al., 1996; Peng et al., 2003). Besides in vitro tests of fibrinolytic activity, many in vivo studies had been reported. (Fujita et al., 1995) treated dogs with nattokinase by oral administration, and the fibrinolytic activity in plasma increased and showed that subtilisin NAT could pass the rat intestinal tract and dissolve the chemically induced thrombosis. (Suzuki et al., 2003) found that dietary supplementation of Natto suppressed intimal thickening and modulated the lysis of mural thrombi after endothelial injury in rat femoral artery. Furthermore, NK can cleave active recombinant prokaryotic plasminogen activator inhibitor into low molecular weight fragments (Urano et al., 2001). Those researches imply that NK is useful as a promising thrombolytic agent (Sumi et al., 1990).
In this paper we report on the isolation and screening of nattokinase producing bacillus sp from soil. UV mutation was also carried out for isolated Bacillus sp. The nattokinase was extracted and precipitated for both normal and UV mutated Bacillus sp and the clot buster activity was studied.
Materials and Methods
Isolation and morphological characterization of Bacillus sp
Soil sample was collected from VIT garden and serially diluted to 10-6. Spread plate technique was performed on Nutrient Agar and incubated at 37°C for 24 hours. The bacterial colonies were selected based on the colony morphology. Pure culture was made and stored at 4°C. To determine the external morphology of the isolation, Grams reaction was performed.
Radial caseinolytic assay
Screening for nattokinase was done using nutrient media supplemented with 2%casein. Culture supernatants were obtained by centrifuging the production media. Wells were made on the solidified casein media using a sterile cork borer (each with one test and one control). 100 µL of the culture supernatants were added and the plates were refrigerated for 4 hours to allow the radial diffusion of the compounds contained in the supernatant prior to incubation for 24 hours at 37°C .
Production of nattokinase (Dubey et al., 2011)
For nattokinase production, two different types of production media were prepared for comparative studies. Production media supplemented with shrimp shells was prepared and 1%inoculum from nutrient broth was transferred to it. It was then incubated in the shaker at 37°C for 2 days. Simultaneously production media without shrimp shell substrate was also prepared and inoculated with 1% inoculum from nutrient broth. It was incubated in the shaker at 37°C for 7 days.
Enzyme separation and precipitation
For the separation of enzyme, the production media was centrifuged at 8,000 rpm for 20 min in a cooling centrifuge at 4°C. Supernatant was collected, which served as the crude enzyme, and used for the enzyme assays and precipitation.
The crude supernatant was subjected to ammonium sulfate precipitation. 30 and 80% of ammonium sulfate was added to each sample with constant stirring for 15 min in magnetic stirrer followed by centrifugation at 10,000 rpm for 30 min. Supernatant was collected and dissolved in 1x phosphate buffer saline. Both the crude and the precipitated enzymes were used to determine the plasmolytic and thrombolytic activity.
Enzyme assay
Plasmolytic activity of the extracted enzyme was determined by the Heated Plasma Agar assay. Nutrient agar was prepared, human blood was freshly collected and an anticoagulant (heparin) was added to it. It was then centrifuged at 10,000 rpm for 10 min. Blood plasma (supernatant) was drawn out and kept in the water bath for 20 min at 56°C. The heated plasma was then cooled to optimum temperature and added to nutrient agar and mixed well by shaking. The resulting media was poured into sterile petriplates. Wells were made on the solidified media using a sterile cork borer (each with one test and one control). 100 µL of the culture supernatants were added and the plates were refrigerated for 4 hours to allow the radial diffusion of the compounds contained in the supernatant prior to incubation for 24 hours at 37ºC.
Determination of enzyme activity
Modified Holmstorm method (Holmstorm, 1965) was used to determine the enzyme activity. Human blood was freshly collected and poured into 1.5 mL eppendorf tubes (each tube containing 1 mL blood). When the blood clotted completely, crude as well as precipitated enzyme solutions were added in increasing concentrations, i.e, 10, 20, 30 µL and so on up to 100 µL separately. After incubating it for 18 hours at 37°C, the tubes were inverted to check the extent of lysis, and the clot lysis activity was determined.
Strain improvement technique
Since, we observed better lysis of the clots by the strain grown in shrimp shell supplemented media and proceeded to carry out strain improvement of the same.
Isolated colonies of Bacillus sp SFN were suspended in 1X PBS and exposed to UV for 2.5, 5, 7.5 and 10 min (Thaer et al., 2005). These plates were kept 20 cm away from the UV lamp (at a wavelength of 254 nm). After the exposure, the suspension was stored overnight in the dark to avoid photo reactivation. Mutated samples were inoculated into the shrimp shell supplemented media and incubated for 2 days at 37°C. Ammonium sulphate precipitation was carried with the culture supernatants using 30, 70 and 80% ammonium sulfate. Samples were then used to perform Holmstorm method to determine the clot lysis activity. A lower concentration of the enzyme (1 to 10 µL) was used this time to compare the efficiency of the enzyme produced by the mutated strains. Extent of lysis was checked after incubating it for 18 hours at 37°C.
High performance liquid chromatography
The precipitated sample of Bacillus sp SFN was subjected to RP-HPLC. The chromatographic conditions used are as follows: Chromatographic column: C18. Mobile phase: 0.2 mol/L of NaH2PO4-CH3OH (95:5). Flow rate: 1 mL/min. Detection wavelength: 220 nm. Total run time: 20 min. Elution peaks were collected and the enzyme purity was determined (Wang et al., 2009) .
Result and Discussion
Our continuous search for Bacillus sp. from soil led to the isolation of one strain of Bacillus which was named as SFN (Search for nattokinase). The Bacillus culture was maintained as pure culture in nutrient agar for further studies. The colony morphology of SFN was creamish, almost circular, flat opaque colonies. The Gram reaction of the SFN colony was found to be gram positive, rod shaped and in pairs.
The screening of nattokinase production was determined by performing the caseinolytic assay. Bacillus sp SFN showed caseinolytic activity on nutrient agar supplemented with 2% casein since the proteolytic enzyme produced by Bacillus sp SFN utilized the casein present in the media. SFN grown in shrimp shell production media showed better activity than Bacillus sp SFN grown on production media without shrimp shell showed comparatively less activity (Figure 1).
Figure 1: Caseinolytic activity of SFN on production media (A) with shrimp shell or (B) without shrimp shell
The plasmolytic activity was checked by the heated plasma agar assay. The enzyme produced by Bacillus sp SFN showed plasmolytic activity on nutrient agar supplemented with blood plasma. Bacillus sp SFN grown in shrimp shell production media showed better activity than the Bacillus sp SFN grown on production media without shrimp shell showed comparatively less activity (Figure 2).
Figure 2: The plate shows zone of clearance where 1 represents Bacillus sp SFN crude in production media without shrimp shell, 2 and 3 represent Bacillus sp SFN crude in production media with shrimp shell and 4 as control
In the holmstorm method, the extent of lysis was checked after the coagulation of blood , in order to determine the enzyme activity. One unit of enzyme activity was defined as the minimum amount of enzyme at which the blood clot lyses completely.
Both the samples Bacillus sp SFN produced in shrimp shell media showed lysis of blood starting from 10 to 100 units. But the Bacillus sp SFN produced in production media showed lysis starting from 20 to 100 units. The following Figure 3 and Figure 4 show lysis after incubation at 37°C for 18 hours.
Figure 3: Holmstorm method for Bacillus sp SFN crude supernatant in production media without shrimp shell (10 to 100 µL)
Figure 4: Holmstorm method for Bacillus sp SFN crude supernatant in production media with shrimp shell (10 to 100 µL)
Therefore, enzyme produced by Bacillus sp SFN in shrimp shell media showed better clot lysis activity, than the production media without shrimp shell.
The samples produced in media without shrimp shell and shrimp shell supplemented media were subjected to ammonium sulfate precipitation and with the 70 and 80% precipitates this Holm storm method was carried out.
The 70 and 80% precipitates of the enzyme produced by Bacillus sp SFN in production media which was added in concentrations of 5, 10, 15 and 20 units showed complete lysis after an incubation period of 18 hours shown in Figure 5.
Figure 5: Holmstorm method for Bacillus sp SFN precipitates in production media without shrimp shell (5, 10, 15, 20 µL)
Similarly the 70 and 80% precipitated enzymes produced by Bacillus sp SFN in shrimp shell media gave complete lysis in all four concentrations (Figure 6).
Figure 6: Holmstorm Method for Bacillus sp SFN precipitates in production media with shrimp shell (5, 10, 15, 20 µL)
The Bacillus sp. SFN grown in shrimp shell showed good result in all the assays. Thus, the Bacillus sp. SFN was mutated by UV-radiation and Holmstorm method was performed.
Clot lysis activity was observed in both 5 and 10 min when exposed to UV radiation. Thus, 5 min of UV exposure was better for the clot lysis by Bacillus sp SFN (Figure 7, Figure 8).
Figure 7: Holmstorm Method for Bacillus sp SFN mutated (5 min) precipitates in production media with shrimp shell (1 to 10 µL)
Figure 8: Holmstorm Method for Bacillus sp SFN mutated (10 min) precipitates in production media with shrimp shell (1 to 10 µL)
Thereby, it can be concluded from the result that 5 and 10 min of exposure time to the mutagen was the most effective in producing favorable mutation that produced nattokinase with a higher activity than the wild strain.
The concentrations of nattokinase obtained from the standard graph are as follows: a) Non mutated Bacillus sp SFN precipitates (grown in shrimp shell supplemented medium) was 570 µg/min; b) Mutated (5 min) Bacillus sp SFN precipitates (grown in shrimp shell supplemented medium) was 460 µg/mL; c) Mutated (5 min) Bacillus sp SFN crude (grown in shrimp shell substituted medium) was 490 µg/mL.
Chromatogram obtained for nattokinase produced by Bacillus sp SFN was compared with standard. The retention time of the nattokinase was found to be 10.6 min.
Conclusion
UV irradiation is an effective mutagenic agent for strain improvement of Bacillus sp. and its enhanced nattokinase activity. One unit of the enzyme from the mutated strain has been found to lyse the clot completely. This could hold great value for the future which would enable one to obtain high yielding mutant strains of these isolations for large scale production of nattokinase.
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