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Purification and characterisation of the extracellular cholesterol oxidase enzyme from Enterococcus hirae



Recently many efforts are being carried out to reduce cholesterol in foods. Out of the 50 selected isolates that were tested using the agar well diffusion method to assess their ability to decompose cholesterol, 24 bacterial isolates were screened based on their cholesterol-decomposition ability in liquid media.


The bacterial isolate that displayed the highest cholesterol oxidase activity was identified as Enterococcus hirae. The maximal growth and cholesterol decomposition were achieved with a 1-day incubation under static conditions at 37 °C in cholesterol basal medium adjusted to pH 7 supplemented with 1 g/l cholesterol as the substrate, no additional carbon or nitrogen sources and 0.5 % CaSO4. The cholesterol oxidase enzyme (ChoX) produced by E. hirae was extracted at an (NH4)2SO4 saturation level of 80 % and purified with 79 % yield, resulting in 2.3-fold purification. The molecular weight of (ChoX) was 60 kDa. The optimal conditions required for the maximal activity of the purified COD enzyme produced by E. hirae were 30 min, 40 °C, pH 7.8, substrate concentration of 1 g/l and 200 ppm of MgCl2. The enzyme maintained approximately 36 % and 58.5 % of its activity after 18 days of storage at 4–8 °C. Also, the enzyme loss its activity by gradual thermal treatment, but it maintained 58.5 % of its activity at 95 °C for 2 hr.


E. hirae Mil-31 isolated from milk had a great capacity to decompose cholesterol in basal medium supplemented with cholesterol under its optimal growth conditions. Decomposition process of cholesterol by this strain results from its production of cholesterol oxidase enzyme (ChoX). The highest specific enzyme activity and highest purification fold of purified enzyme were achieved after using Sephadex G-100.


Cholesterol is a waxy, fat-like substance that is found in all cells of the body. Cholesterol enters the human body mainly through food [1], and the majority of the cholesterol in the body originates from the liver [2]. Cholesterol is required for the formation of sex hormones [3], Cholesterol can also be converted to bile acids in the liver and vitamin D in the skin and kidney [4] and the formation of bile acids that help the body to digest fat [5]. Many studies have reported the ability of different bacteria to reduce the cholesterol levels in aqueous systems, such as liquid media [6] and the blood serum [7].

Some bacteria not only utilize cholesterol as a sole carbon source [8] but also decompose cholesterol via the cholesterol oxidase enzyme (ChoX) and produce different intermediate compounds [9]. Enterococcus faecium CX and Lactobacillus acidophilus N5, which colonise the intestinal tract and survive under gastric conditions, assimilate cholesterol and reduce its level in serum [10]. Pereira and Gibson (2002) [11] found that Lactobacillus fermentum strains F53 and KC5b, Bifidobacterium infantis ATCC 15697, Enterococcus durans DSM 20633, Enterococcus gallinarum, and Enterococcus faecalis have in vitro cholesterol-reducing abilities [11].

A variety of ChoX enzyme producing microorganisms have been isolated by [12], most of them produce cell-bound ChoX enzyme, but some Actinomycetes are able to produce high levels of extracellular ChoX enzyme, which is generally easier for isolation and purification than intracellular enzymes [12]. Streptomyces sp. produce COD enzyme extracellularly [13] and the corresponding structure gene for COD enzyme has been cloned and sequenced from different Streptomyces as Streptomyces fradiae [14], Streptomyces natalensis [15]. Gamma-proteobacterium Y-134 [16], Burkholderia cepacia [17], Cellulomonas [18], Brevibacterium sterolicum [19], Brevibacterium sp. [20], also produce extracellular COD enzyme.

Cholesterol degrading bacteria from cow’s milk and about 11 bacterial isolates exhibited cholesterol degrading activity with cholesterol lowering potentials ranging from 42.88 –97.20 % [21]. The ChoX enzyme from Burkholderia cepacia strain ST-200 produces 6-beta-hydroperoxycholest-4-en-3-one from cholesterol [22]. The oxidation of cholesterol produces the intermediate 3-ketosteroid as the final product [23]. Cholesta-4, 6-dien-3-ol, cholesta-4, 6-dien-3-one, and cholesta-3, 5-dien-7-one are produced from the oxidation of cholesterol [9]. Doukyu and Aono (2001) [22] reported that the ChoX enzyme from Burkholderia cepacia strain ST-200 produces 6-beta-hydroperoxycholest-4-en-3-one from cholesterol. The oxidation of cholesterol produces the intermediate 3-ketosteroid as the final product [23]. Liu and Shan (2006) [9] reported that cholesta-4,6-dien-3-ol, cholesta-4,6-dien-3-one, and cholesta-3,5-dien-7-one are produced through the oxidation of cholesterol. Numerous factors affecting the activity of the cholesterol oxidase enzyme have been studied by many different research groups [24, 25].

The optimisation of culture conditions is an important consideration when studying cholesterol oxidase enzymes in bacteria. In particular, the culture conditions influence the properties of the enzyme [25, 26].

Purification and characterisation of several microbial cholesterol oxidase enzymes were conducted by [14, 24]. Niwas et al. (2014) [27] suggested that calcium alginate entrapment is a promising method for the immobilisation of Streptomyces sp. and also suggested that the immobilized cells may produce ChoX at higher quantities after three consecutive fermentation cycles compared with free cells. The results obtained can be exploited for commercial purposes. Lashkarian et al. (2010) [28], were instructed a recombinant plasmid containing ChoX gene from Rhodococcus sp. strain 50, cloned into cloning vector (STV28) and transformed into E. coli strain DH5α to produce a significant levels of extracellular ChoX in an optimized medium for a short period.

The importance of the ChoX enzyme is derived from the biotechnological purposes for which the enzyme is applied. This enzyme is industrially important for the production of pharmaceutical steroids [29], determination of cholesterol in food by coupling with peroxides [30], determination of the total cholesterol in several real food samples such as eggs and meat [31], and in agriculture for insecticides [32]. This ChoX enzyme is widely used for bioconversions for the clinical determination of blood serum cholesterol [30].

The objectives of this study are the enumeration and isolation of cholesterol-decomposing bacteria from different sources, the screening of isolates based on their ability to decompose cholesterol in liquid media, the optimisation of some growth conditions for maximal cholesterol decomposition, and the production, purification and characterisation of the ChoX enzyme produced by the most active isolates.


Enumeration and isolation of cholesterol decomposing bacteria

Different food samples (n =100) from many sources were collected from local markets located in Zagazig city located in Egypt. 20 samples of each product were collected (cheese, yogurt, raw milk, whey and milk). The spread plate technique [33] and basal medium [34] were used. The Medium was prepared as follows (g/l): NH4Cl, 0.5; NaCl, 0.5; KH2PO4, 0.4; K2HPO4, 0.3; MgSO4, 0.2; yeast extract, 0.1; agar 20 g; and distilled water up to 1000 ml, pH 7 ± 0.2. Cholesterol was added at a concentration of 1 g/l [35]. The media did not contain a carbon source (cholesterol), but it was sterilised separately. Cholesterol was emulsified according to method described by Imshenetskii et al. (1968) [36], where 1 g of cholesterol was dissolved in 35 ml of boiling acetone. Then added to 200 ml of distilled water heated to 90–95 °C drop-by-drop. Then it was filtered, condensed under vacuum to remove the acetone. The resulting cholesterol emulsion was sterilized at 0.5 atm. for 30 min [37] then the solution was stored in a refrigerator. The ability of bacteria to decompose cholesterol was estimated by the appearance of clear zones of translucency around colonies on agar medium after incubation at 37 °C for 24 h [37]. The numbers of cholesterol decomposing bacteria were determined.

Screening of bacterial isolates for cholesterol decomposition

  1. a)

    Well diffusion agar method:

    • All bacterial isolates were purified and maintained in the basal media and tested for cholesterol decomposition using the well diffusion agar method as described [38].

  2. b)

    In liquid medium:

    • The experiment was carried out to select the most potent bacterial isolates that have the high percent of cholesterol decomposition added in their liquid medium. Cholesterol was quantitatively measured using a colourimetric method (Liebrman-Burchard reaction [39]. The residual cholesterol was calculated according to the equation of [17] as follows:

    • Residual cholesterol (mg/dl) = Absorption of standard/Absorption of standard × Conc. of standard.

    • The amount of decomposed cholesterol (mg/dl) = Amount of cholesterol in control – Amount of residual cholesterol of sample.

    • The % of cholesterol decomposition = Amount of decomposed cholesterol/Amount of cholesterol in control × 100.

Identification of the most abundant producer bacterial isolates

The most active ChoX enzyme producer isolate was identified using a Biolog Microlog 34.20 system at the Unit of Identification of Microorganisms and the Biological Control Unit of the Agriculture Research Centre, Giza, Egypt.

Some factors affecting the growth and decomposition of cholesterol by the tested bacteria in liquid media

For studying the factors affecting the growth of bacterial strain and decomposition of cholesterol, constant condition was used throughout the study as follows: conical flasks (250 ml in volume) containing 100 ml of fermentation broth basal medium [34] and contained 0.1 g cholesterol were inoculated with one ml of standard inoculum of the bacterial strain cultures and incubated at 37 °C for 24 h. Some growth factors affecting cholesterol decomposition were studied, such as different incubation temperatures (20 to 50 °C) and incubation periods (1 to 3 days); different pH values using acetate buffer (pH 3.6 up to 5.6) and phosphate buffer (pH 6 up to 8) to adjust the pH; static and shaking conditions at different speeds (80 to 140 rpm); different concentrations of cholesterol such as 0.5 to 2 (g/l); different carbon sources (glucose, fructose, sucrose, maltose, lactose, galactose and glycerol) at a final concentration of the carbon source 1 % w/v [40]; organic nitrogen sources (peptone, yeast extract and beef extract) at a final concentration of medium 0.5 %, w/v [40]. Inorganic nitrogen sources (potassium nitrate, sodium nitrate and ammonium sulphate) at a final concentration equimolecular to that in 3 g of NaNO3, different concentrations of metals (BaCl2, MnCl2, CaSO4, Na2HpO4, K2HpO4 and MgSO4) and different growth media (nutrient, yeast and basal medium) were also studied. The bacterial strain was grown at different parameters then cholesterol decomposition assay was performed.

ChoX enzyme assay

The activity of the extracellular enzyme was determined according to the method described by Inouye et al. (1982) [41], as follows: to 0.4 ml of 125 mM Tris-HCl buffer pH 7.5, 0.1 ml of cell free extract was added, and the mixture was incubated in water bath at 37 °C. After 3 min. 25 μl of 12 mM of cholesterol in isopropanol solution were added to the mixture, then after 30 min., 2.5 ml of absolute ethanol were added to the reaction medium and the amount of 4-cholesten-3-one was determined by measurement of the absorbance at 240 nm. Reaction blanks were prepared by replacing 25 μl of cholesterol solution for 25 μl of isopropanol. Then ChoX activity (U/ml) and ChoX specific activity (U/mg. protein) were calculated.

One unit of cholesterol oxidase activity (U): was defined as that which brings about the formation of 1 μmol of 4-cholesten-3-one in 30 minutes at 37 °C.

Protein estimation

Protein was estimated by the method of Lowry et al. (1951) [42], using bovine serum albumin (10 – 100 μg/ml) as a standard measured at 750 nm.

Purification of ChoX enzyme

Ammonium sulphate was added to the culture filtrate up to 80 % saturation for the partial purification of the enzyme. The precipitate was dissolved in 10 mM 0.2 M Tris-HCl buffer, pH 8. The precipitate was then dialysed against the same buffer. This preparation was applied to a Sephadex G-100 gel chromatography column. Fifty fractions (each containing 5 ml) were collected at 1 ml/min. Both enzyme activity and protein content were determined for each separate fraction. The molecular weight of the purified cholesterol oxidase enzyme produced by E. hirae was determined by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS–PAGE), which was performed according to the method [43], as modified [44] at the Agriculture Genetic Engineering Research Institute (AGERI), Giza, Egypt.

Factors affecting the activity of purified ChoX enzyme

The effect of different concentrations of enzyme (0.1 to 0.7 mg/ml) at different incubation periods (10 to 90 min); different incubation temperatures (20 to 55 °C); different pH values (7.2 to 9.0) by adjusting pH with 0.2 M Tris-HCl buffer); different cholesterol concentrations (0.25 to 1.75 (g/l)); different metal ions (EDTA, cadmium chloride, manganese chloride, potassium chloride and cobalt chloride) at different concentrations (100 to 300 PPM); and different storage periods (2 to 18 days) were estimated (1 ml of cholesterol emulsion (1 g/l) added to different concentrations of enzyme (0.29 to 1.45 mg protein/ml) were incubated for 30 min at 37 °C. The enzyme activity at each concentration was determined as previously mentioned). Additionally, the thermal stability of purified ChoX was studied at 45 to 95 °C for 2 h.

The obtained data were statistically analysed to determine the standard deviation, and differences between means were assessed as described [45]. Bivariate correlation matrix analysis of the obtained data was performed using SPSS software program (Version 8) as described [46].

Results and discussion

Cholesterol decomposing bacteria were enumerated and isolated from different food samples (n = 20 for each) namely yogurt, whey, milk, cheese and raw milk using basal cholesterol medium and dilution method. It was obvious from the obtained results in Table 1, that there were no noticeable differences in the counts of these microorganisms in the tested samples. Also it was found that the highest bacterial count was found in yogurt (Log N = 6.4), followed by raw milk and milk (values of 6.38 and 6.37, respectively) while the lowest bacterial count was represented in cheese and whey (6.35 and 6.28 respectively. Fifty bacterial isolates were screened for cholesterol decomposition on basal cholesterol agar medium using the well diffusion agar method. Out of 50 cholesterol decomposing isolates, only 24 bacterial isolates were selected for further screening due to their decomposition of cholesterol added to their liquid media. The highest percentages of cholesterol decomposition (75.3, 69.8, 60.08 and 54.8 %) were recorded for bacterial isolates M-31, Ch-14, Y-28 and W-42, respectively. The mean percent cover value for the five foods were analysed by Duncan’s multiple range test. This test revealed that mean within the column was not significantly different due to the difference among bacterial.

Table 1 Screening of bacterial isolates for cholesterol (100 mg/dl) decomposition in liquid medium and total viable count on solid medium (Log N)

The highly active cholesterol-decomposing isolate M-31 was selected and identified as Enterococcus hirae using a Biolog Microlog 34.20 System at the Unit of Microorganisms, Identification of Microorganisms and Biological Control Unit of the Agriculture Research Center, Giza, Egypt. In this study, different factors affecting the growth and cholesterol decomposition by E. hirae were studied. The results shown in Fig. 1a , demonstrate that the maximal cholesterol decomposition (75.1 %) in liquid medium was achieved after one day. The results presented in Fig. 1b show that the maximal percentage of cholesterol decomposition (74.2 %) in liquid medium by E. hirae was obtained at 37 °C. Above and below this particular incubation time there was a reduction in the ability of tested bacteria to cholesterol decomposition. Food is considered a good source of cholesterol decomposing microorganisms. Pathogenic mycobacteria are able to take up, modify, and accumulate cholesterol from liquid growth media and form a zone of clearance aound a colony when plated on solid media containing cholesterol [47]. The reduction of cholesterol levels in vitro or in vivo by microorganisms may take place via non-enzymatic [12] or enzymatic processes [8]. The latter bacteria may decompose cholesterol due to their production of extracellular cholesterol oxidase (ChoX) enzyme. These results are in agreement with [48], who reported that some intestinal bacteria such as Bifidobacterium, Eubacterium, Lactobacillus, Enterobacteriaceae, Clostridium and Enterococcus decompose cholesterol via the ChoX enzyme to cholest-4-en-3-one. Additionally [13], reported that cholesterol might be completely oxidised by microbial ChoX to generate carbon dioxide and water. Moreover, Cellulomonas [18], Brevibacterium sterolicum [28], Streptomyces natalensis [15] and Brevibacterium sp. [20] are ChoX -producing bacteria.

Fig. 1
figure 1

(a, b, c and d) Effect of different Incubation periods, temperatures, pH value, static and shaking conditions on the biomass and cholesterol decomposition by E. hirae respectively. Difference between values is statistically significance level of 0.05

Environmental and nutritional factors are known to influence the growth and decomposition of cholesterol by microorganisms. The optimisation of these culture conditions was achieved by Chang and Chou (2002) [49] and Kim et al. (2003) [25]. The optimum temperature for the decomposition of cholesterol in liquid medium by Brevibacterium sp. was 37 °C [13]. In contrast, several studies have reported other optimal incubation temperatures, such as 34 °C for Streptomyces fradiae [14], 29 °C for Rhodococcus erythropolis ATCC 25544 [24] and 30 °C for Bacillus subtilis SFF34 [28].

Moreover, the results in Fig. 1c, show that pH 7.0 was the optimum pH value for cholesterol decomposition (80.2 %) in liquid medium by E. hirae. It was found that, optimal pH value required for attaining maximum growth and decomposition of cholesterol by E. hirae was pH 7.0 using 0.2 M acetate buffer and 0.2 M phosphate buffer.

In contrast, the pH value of the culture medium plays a critical role in the optimal physiological performance of the cells and the transport of various nutrient components across the cell membrane, and the decomposition of cholesterol is affected by a change in the pH value of the media. It was previously reported that the optimal pH values for cholesterol decomposition are 7.2 for Streptomyces fradiae [14] and 6.75 for Rhodococcus erythropolis ATCC 25544 [24].

The results in Fig. 1d, show that static conditions were better than shaking conditions for the decomposition of cholesterol by the tested strain in the liquid media. Additionally, the results indicate that the highest percentage of cholesterol decomposition by E. hirae was (80.1 %). E. hirae favored static condition for growth and decomposition of cholesterol than shaking conditions. Although shaking conditions are generally better than static conditions for the optimal cholesterol decomposition of aerobic bacteria [14, 50], this doesn’t apply for the facultative anaerobic bacteria [51]. Sabry (1994) [50] reported that a shaking speed of 120 rpm is optimal for Pseudonocardia compacta S-39, whereas a shaking speed of 150 rpm is optimal for Streptomyces fradiae [14].

The results in Fig. 2a, show that the maximum percentage of cholesterol decomposition (80.2 %) by the E. hirae strain was achieved at 1 g/l cholesterol added (control sample). The present investigation detected that, the growth and decomposition of cholesterol by the tested bacterial isolates were greatly affected by cholesterol concentration in the cultural medium, whereas maximal cholesterol decomposition by Streptomyces fradiae (Yazdi et al., 2001) [14] and Rhodococcus erythropolis ATCC 25544 (Sojo et al., 2002) [24] was obtained with 2 gm/l.

Fig. 2
figure 2

(a, b, c and d): Effect of different concentration of cholesterol, carbon sources, nitrogen sources and different metal ions on the biomass and cholesterol decomposition by E. hirae respectively. Difference between values is statistically significance level of 0.05

The results in Fig. 2b and c show that the maximum cholesterol decomposition (75.3 %) by E. hirae was obtained when the growth medium lacked any additional carbon or nitrogen source (control sample). The inhibitory effect of different carbohydrates on ChoX enzyme production may be due to the decrease in bacterial ability to metabolite these carbohydrates, suggesting that, the enzyme play an important role in bacterial metabolism These results agree with those presented by [8] who reported that the Lactobacillus, Streptococcus, Enterococcus and Leuconostoc genera use cholesterol as a source of carbon. Sabry (1994) [50] observed that glycerol and xylose are the best carbon sources for the decomposition of cholesterol and glucose, and the use of starch as a carbon source resulted in a lower percentage of cholesterol decomposition by Pseudonocardia compacta S-39. This researcher also reported that sodium nitrate, ammonium sulphate and ammonium nitrate are the best nitrogen sources for cholesterol decomposition by Pseudonocardia compacta S-39.

The results in Fig. 2d, show the percentages of cholesterol decomposition achieved by each tested strain in the presence of metal ions. The results showed that highest percentage of cholesterol decomposition of 82.5 % was achieved with liquid media supplemented with 0.5 % CaSO4. Metal ions affecting on the growth and decomposition of cholesterol in liquid medium by E. hirae. In addition, the results shown in Figs. 1 and 2 show that increasing or decreasing the growth (dry weight) of E. hirae led to a corresponding increase or decrease in the percent of cholesterol decomposition.

The maximum percentage of cholesterol decomposition (80.4 %) by E. hirae was achieved using the basal medium. This result may be because the basal medium is suitable for enzyme production and activity because it contains minerals that act as a prosthetic group for the enzyme. Leland (1976) [52] recorded that the inactivation of enzyme by metals may be due to the binding of metal to the prosthetic groups of enzymes (oligodynamic effect). Sabry (1994) [50] observed that 0.04-0.1 % (w/v) of MgSO4 and 0.01-0.02 % (w/v) of K2HpO4 were most favourable for cholesterase production by Pseudonocardia compacta S-39. Gruber et al., (1979) [53] found that it is possible to increase the cholesterol oxidase content of the said microorganisms several fold and at the same time to double the dry bacterial mass per liter of culture solution. The activity of cholesterol oxidase is directly and sensitively dependent on the physical properties of the membrane into the active site in which its substrate is bound [54].

A summary of the purification data of ChoX enzyme produced by E. hirae is presented in Table 2 and Figs. 3 and 4. Our results showed that the partial purification of the enzyme increased the enzyme’s specific activity from 53.30 ± 0.02 to 124.87 ± 0.02 (U/mg protein), which corresponds to 2.3-fold purification and 79 % yield at the Sephadex G-100 purification step. It was shown that subsequent steps of purification program for E. hirae which have been carried out, the resultant precipitate was dissolved in a least amount of 10mMTris HCl buffer pH 8.0, and then it was dialysed against distilled water to exclude the sulphate ions. Furthermore it was concentrated by dialysis against sucrose crystals and consequently applied to Sephadex G-100 column chromatography. Active fractions of the sharp peak of fractional purification curve were collected and concentrated by dialysis against the same buffer for having a concentrated preparation of the purified cholesterol oxidase enzyme.

Table 2 Summary of purification steps
Fig. 3
figure 3

Fractional precipitation of crude cholesterol oxidase enzyme by ammonium sulphate saturation levels. The difference between values is statistically significance level of 0.05

Fig. 4
figure 4

Fractional purification pattern of the dialysed cholesterol oxidase enzyme by Sephadex G-100 column chromatography

The present study was extended for the purification and characterisation of ChoX enzyme produced by E. hirae. Our results are in agreement with that of [12], who recorded an optimum pH of 6.8 to 8.0 for the purified ChoX produced by Pseudomonas sp. However, [13] reported that the optimum pH value for purified ChoX activity for Brevibacterium sp. ranged from 5.0 to 7.5 when using 10.0 mM phosphate buffer, while 50 mM Tris–HCl buffer increased the optimum pH value to 8.0 to 8.8. In addition, the maximal production occurred at pH 6.5 for Brevibacterium sterolicum nov. sp. ATCC21387 [29].

Table 3 shows the maximum enzyme activity (90.2 U/ml( of the purified enzyme was achieved at 30 min. The enzyme activity was enhanced by increasing the incubation temperature up to 40 °C at which the optimum enzyme activity (84.1 U/ml) was found. The maximum cholesterol oxidase activity (89.8 U/ml) was obtained at pH 7.8 using 0.2 M Tris-HCl buffer, incubated at 40 °C for 30 min. The optimum cholesterol concentration for maximum enzyme activity (90.1 U/ml) was achieved at 1 g/l cholesterol. The maximum enzyme activity of the purified enzyme found in our study agreed with that reported by [14] for Streptomyces fradiae, whereas [28] noted that 1 min was optimal for Bacillus subtilis SFF34. The enzyme activity was enhanced by increasing the incubation temperature. However, other authors reported that the temperature of 53 °C was optimal for cholesterol oxidase activity from Brevibacterium sp. [13], while [14, 29] reported optimum temperatures of 70 and 55 °C for the ChoX enzyme purified from Streptomyces fradiae and Brevibacterium sterolicum nov. sp. ATCC21387, respectively. The optimum cholesterol concentration for maximum enzyme activity was in agreement with [55]. Tietz (1994) [55] reported that the rate of enzymatic reaction is generally proportional to the concentration of the enzyme. In addition to the incubation period of the enzyme and substrate, the storage time of the purified enzyme also affects ChoX enzyme activity.

Table 3 Effect of different incubation temperatures, pH values, substrate (cholesterol) concentrations on the cholesterol oxidase activity produced by E. hirae Mil−31
Table 4 Effect of different activators and inhibitors on the cholesterol oxidase activity of the enzyme produced by E. hirae

We also found that the molecular weight of the purified cholesterol oxidase enzyme produced by E. hirae is 60 kDa, in comparison with the standard protein markers. as shown in Fig. 5. Moreover, different factors that affect the purified cholesterol oxidase enzyme produced by E. hirae were studied and indicated that the continuous increase in cholesterol oxidase activity is due to the corresponding linear increase in the enzyme concentration. The same molecular weight of ChoX enzyme purified from Streptomyces fradia and Rhodococcus erythropolis ATCC 25544 [1424]. However, the molecular weights of ChoX enzyme purified from Burkholderia cepacia [17], Streptomyces sp. SA-COO [56] and Gamma-proteobacterium Y-134 [16] were 58.7, 55 and 58 kDa, respectively. This finding is in agreement with [50], who reported that the rate of an enzymatic reaction is generally proportional to the enzyme concentration. Praveen et al. (2011) [57] purified the extracellular cholesterol oxidase (cho) enzyme from Streptomyces parvus as a new source, and 18-fold purification was achieved by ion-exchange and gel filtration chromatography. The specific activity of the purified enzyme was found to be 20 U/mg with a 55 kDa molecular mass.

Fig. 5
figure 5

The molecular weight of the purified cholesterol oxidase enzyme produced by Enterococcus hirae on SDS- PAGE (15 % acrylamide) and stained with coomassie brilliant blue dye

Regarding to thermal stability of the purified ChoX enzyme produced by E. hirae, the results presented in Fig. 6 show that 45–55 °C was the optimal temperature range for activity of the purified ChoX enzyme (82.4 and 82.1 U/ml(. In addition, although increasing the temperature reduced the enzyme activity, approximately 58.5 % of the COD enzyme activity was maintained at the high temperature of 95 °C. Enzyme inactivation may be due to protein denaturation at the high temperature and consequently affected the reaction rate. Salva et al. (1999) [13] found that the thermal stability for Brevibacterium sp. was 40 °C. Yazdi et al. (2001) [14] reported that the thermal stability of ChoX produced by Streptomyces fradiae was very high. ChoX had full activity at 50 °C after 90 min in 0.1 M phosphate buffer at pH 7.0. They also added that the enzyme was stable at 60 °C for 20 min. Metal ions were also observed to influence the activity of ChoX purified from E. hirae. Calcium alginate entrapment is a promising method for the immobilisation of Streptomyces sp. and also suggested that the immobilised cells could be used for three consecutive fermentation cycles for ChoX production in higher quantities compared with free cells [27]. The results obtained can be exploited for commercial purposes. In contrast, the enzyme was stable for one week when stored at 2–8 °C [50]. The enzyme activity was reduced after two weeks and continued to decrease gradually until it was completely lost at the end of 14 weeks. However, Salva et al. (1999) [13] reported that for Brevibacterium sp., the maximum enzyme activity was stable up to 15 days of storage and activity was lost at 30 days. Inactivation of the enzyme may be due to protein denaturation resulting from the high temperature, which consequently affected the rate of reaction.

Fig. 6
figure 6

Effect of different temperature stability of the activity of the cholesterol oxidase produced by E. hirae. The differences between values are statistically significant ± LSD at a probability of 0.05

Through this research the relation effect of different activators and inhibitors on the activity of the purified ChoX enzyme produced by E. hirae was studied. The results shown in Table 4, indicate that MgCl2 (200 PPM) and KCl (100 PPM) induced the maximum enzyme activity to 94.4 and 91.2 U/ml, respectively. However, EDTA, COCl2 and CdCl2 had an inhibitory effect. Leland (1976) [52] reported that the stimulatory effect of metals on enzyme activity might be related to the fact that metals act as a binding link between the enzyme and substrate or they may act as a coenzyme. Alternatively, the inhibitory effect may be related to binding of the metal to prosthetic groups of the enzyme. This finding is in agreement with [58], who observed that Mg++ is the best inducer for exo-enzymes at 250 μg/ml and for endo-enzymes at 100 μg/ml, while Cd++, Co++, Ba++, and Ca++ ions were endo-enzyme inhibitors. On the other hand, Sabry (1994) [50] observed that 100 μg MgSO4 was the most stimulatory of the metal ions, followed by 50 μg ZnSO4 for the exo-enzyme produced by Pseudonocardia compact S-. It can be concluded that E. hirae produced ChoX enzyme and that the percent of cholesterol decomposition varied according to enzyme production conditions. Additionally, the purification and characterisation of ChoX enzyme enhanced cholesterol decomposition under certain conditions.


Some species of genus Enterococcus which colonize the intestinal tract and reduce cholesterol level in serum. E. hirae Mil-31 isolated from milk had a great capacity to decompose cholesterol in basal medium supplemented with cholesterol under its optimal growth conditions (one day incubation at 37 °C, pH 7 under static condition and 1 g/l cholesterol). Decomposition process of cholesterol by this strain results from its production of cholesterol oxidase enzyme (ChoX). The highest specific enzyme activity and highest purification fold of purified enzyme were achieved after using Sephadex G-100. Also, purification and characterization of ChoX enzyme enhanced the cholesterol decomposition under certain conditions (1.45 mg.protein/ml of enzyme was incubated for 30 min at 40 °C; pH 7.8; 1 (g/l) of substrate and 200 PPM of MgCl2).


  1. Paniangvait P, King AJ, Jones AD, German BG. Cholesterol oxidase in foods of animal origin. J Food Sci. 1995;60:1159–74.

    Article  CAS  Google Scholar 

  2. Fletouris DJ, Botsoglou NA, Psomas E, Mantis AI. Rapid determination of cholesterol in milk and milk products by direct Saponification and capillary gas chromatography. J Dairy Sci. 1998;81:2833–40.

    Article  CAS  PubMed  Google Scholar 

  3. Young DS. Effects of diseases on Clinical lab. Tests. 4th ed. Washington, D.C: AACC press; 2001.

    Google Scholar 

  4. Rigotti A, Miettinen HE, Krieger M. The role of the high-density lipoprotein receptor sr-bi in the lipid metabolism of endocrine and other tissues. Endocr Rev. 2003;24(3):357–87.

    Article  CAS  PubMed  Google Scholar 

  5. Russell DW. The enzymes, regulation and genetics of bile acids synthesis. Annu Rev Biochem. 2003;72:137–74.

    Article  CAS  PubMed  Google Scholar 

  6. Saavedra L, Taranto MP, Sesma F, de Valadez GF. Homemade traditional cheeses for the isolation of probiotic Enterococcus faecium strains. J Food Microbiol. 2004;97(2):231.

    Article  CAS  Google Scholar 

  7. Hlivak P, Odraska J, Ferencik M, Ebringer L, Jahnova E, Mikes Z. One-year application of probiotic strain Enterococcus faecium M-74 decreases serum cholesterol levels. J Bratisl Lek Listy. 2005;106(2):67–72.

    CAS  Google Scholar 

  8. Kovalenko NK, Kasumova SA, Muchnik FV. Screening of the strains of Lactic acid bacteria possessing hypocholesterinemic activity and their practical use. J Mikrobiol Z. 2004;66(3):33–42.

    CAS  Google Scholar 

  9. Liu ZQ, Shan HY. Cholesterol, not polyunsaturated fatty acids, is target molecule in oxidation induced by reactive oxygen species in membrane of human erythrocytes. J Cell Biochem Biophys. 2006;45(2):185–93.

    Article  CAS  Google Scholar 

  10. Zacconi C, Bottazzi V, Rebecchi A, Bosi E, Sarra PG, Tagliaferri L. Serum cholesterol levels in axenic mice colonized with Enterococcus facium and Lactobacillus acidophilus. Microbiologia. 1992;15(4):413–7.

    CAS  Google Scholar 

  11. Pereira DI, Gibson GR. Cholesterol assimilation by Lactic acid bacteria and Bifidobacteria isolated from the human gut. J Appl Environ Microbiol. 2002;68(9):4689–93.

    Article  CAS  Google Scholar 

  12. Doukyu N, Aono R. Purification of extracellular cholesterol oxidase with high activity in the presence of organic solvents from Pseudomonas sp. Strain St-200. Appl Environ Microbiol. 1998;64:1929–32.

  13. Salva TJG, Liserre AM, Moretto AL, Zullo MAT, Ventrucci G, Menezes TJB. Some enzymatic properties of cholesterol oxidase produced by Brevibacterium sp. ISSN 0001-3714. Rev Microbiol. 1999;30:315–23.

    Article  CAS  Google Scholar 

  14. Yazdi MT, Zahraei M, Aghaepour K, Kamranpour N. Purification and partial characterization of a cholesterol oxidase from Streptomyces fradiae. Enzy Microb Tech. 2001;28:410–4.

    Article  CAS  Google Scholar 

  15. Mendes MV, Recio E, Anton N, Guerra SM, Santos-Aberturas J, Martin JF, et al. Cholesterol oxidases act as signaling proteins for the biosynthesis of the polyene macrolide pimaricin. J Chem Biol. 2007;14(3):238–41.

    Article  Google Scholar 

  16. Isobe K, Mori N, Wakao N. The second cholesterol oxidase produced by Gamma-proteobacterium Y-134. J Biosci Bioeng. 2003;96(3):257–61.

    Article  CAS  PubMed  Google Scholar 

  17. Aunpad R, Muench SP, Baker PJ, Sedelnikova S, Panbangred W, Doukyu N, et al. Crystallization and preliminary X-ray crystallographic studies on the class II cholesterol oxidase from Burkholderia cepacia containing bound flavin. Krebs Institute for Biomolecular Research, Department of Molecular Biology and Biotechnology. The University of Sheffield, England. 2002;58(12):2182–3.

    Google Scholar 

  18. Srisawasdi P, Jearanaikoon P, Kroll MH, Lolekha PH. Performance characteristics of cholesterol oxidase for kinetic determination of total cholesterol. J Clin Lab Anal. 2005;19(6):247–52.

    Article  CAS  PubMed  Google Scholar 

  19. Lim L, Molla G, Guinn N, Ghisla S, Pollegioni L, Vrielink A. Structural and kinetic analyses of the H121A mutant of cholesterol oxidase. J Biochem. 2006;400(1):13–22.

    Article  CAS  Google Scholar 

  20. Wang L, Wang W. Coenzyme precursor-assisted expression of a cholesterol oxidase from Brevibacterium sp. in Escherichia coli. Biotechnol Lett. 2007;29(5):761–6.

    Article  CAS  PubMed  Google Scholar 

  21. Kulkarni NS, Lokhande AP, Pachori RR, Agrawal PN, Dalal JM. Screening of the Cholesterol Degrading Bacteria from Cow’s Milk. Curr Res Microbiol Biotechnol. 2013;1(3):92–4.

    Google Scholar 

  22. Doukyu N, Aono R. Cloning, sequence analysis and expression of a gene encoding an organic solvent- and detergent-tolerant cholesterol oxidase of Burkholderia cepacia strain ST-200. J Appl Microbiol Biotechnol. 2001;57(1-2):146–52.

    Article  CAS  Google Scholar 

  23. Motteran L, Pilone MS, Molla G, Ghisla S, Pollegioni L. Cholesterol oxidase from Brevibacterium sterolicum. The relationship between covalent flavinylation and redox properties. J Biol Chem. 2001;276(21):18024–30.

    Article  CAS  PubMed  Google Scholar 

  24. Sojo MM, Bru RR, Garcia FF. Rhodococcus erythropolis ATCC 25544 as a suitable source of cholesterol oxidase: cell-linked and extracellular enzyme synthesis, purification and concentration. BMC Biotechnol. 2002;2:3. 1-9.

    Article  PubMed Central  PubMed  Google Scholar 

  25. Kim KP, Rhee CH, Park HD. Degradation of cholesterol by Bacillus subtilus SFF34 isolated from Korean traditional fermented flatfish. Lett Appl Microbiol. 2003;5:468–72.

    Google Scholar 

  26. Fujishiro K, Uchida H, Shimokawa K, Nakano M, Sano F, Ohta T, et al. Purification and properties of a new Brevibacterium sterolicum cholesterol oxidase produced by E. coli MM294/pnH10. J Microbiol. 2002;215(2):243–8.

    CAS  Google Scholar 

  27. Niwas R, Singh V, Singh R, Pant G, Mitra K, Tripathi CK. Cholesterol oxidase production from entrapped cells of Streptomyces sp. J Basic Microbiol. 2014;54:1233–9.

    Article  CAS  PubMed  Google Scholar 

  28. Lashkarian H, Raheb J, Shahzamani K, Hossein S, Shamsara M. Extracellular Cholesterol Oxidase from Rhodococcus sp. Isolation and Molecular Characterization. Iran Biomed J. 2010;4(1 & 2):49–57.

  29. Lee CY, Liu WH. Production of androsta-1, 4-dien-3, 1, 7-dione from cholesterol using immobilized growing cells of Mycobacterium sp. NRRLB-3683 adsorbed on solid carries. Appl Microbiol Biotechnol. 1992;36:598–603.

    CAS  PubMed  Google Scholar 

  30. Srisawasdi P, Jearanaikoon P, Wetprasit N, Sriwanthana B, Kroll MH, Lolekha PH. Application of Streptomyces and Brevibacterium cholesterol oxidase for total serum cholesterol assay by the enzymatic kinetic method. Division of Clinical chemistry, Department of Pathology, Mahidol University, Thailand. 2006;372(1-2):103–11.

    CAS  Google Scholar 

  31. Basu AK, Chattopadhyay P, Roychoudhuri U, Chakraborty R. Development of cholesterol biosensor based on immobilized cholesterol esterase and cholesterol oxidase on oxygen electrode for the determination of total cholesterol in food samples. J Bioelectrochem. 2007;70(2):375–9.

    Article  CAS  Google Scholar 

  32. Santos RC, Monnerate RG, de SA MdFG, Cordeiro CMT, Gomes AC, Gander ES. Cholesterol oxidase interference on the emergence and viability of cotton boll weevil larva. Pesq agropec bras Brasília. 2002;7(11):1525–30.

    Article  Google Scholar 

  33. Wollum AG. Cultural methods for soil microorganisms. In: Methods of Soil Analysis, Part 2.Chemical and Microbiological Properties-Agronomy Monograph no.9. 2nd ed. Segoe RD., Madison, WI 53711, USA: ASA-SSSA,677S; 1982.

    Google Scholar 

  34. Kumer CG, Joo H, Koo Y, Paik SR, Chang C. Thermostable alkaline protease from a novel marine haloalkalophilic Bacillus clausii. W J Microbiol Biotechnology. 2004;20:351–7.

    Article  Google Scholar 

  35. Turfitt GE. Microbiological genetics in the degradation of steroid .II-Steroid. Utilization by the microflora of soils. J Bact. 1947;54:557.

    PubMed Central  CAS  Google Scholar 

  36. Imshenetskii AA, Efimochkina EF, Zanin VA, Nikitin LE. Decomposition of cholesterol by Mycobacteria. Mikrobiologia. 1968;37:31.

    CAS  Google Scholar 

  37. Zanin VA. Decomposition of cholesterol by Actinomycetes. Microbiologiya. 1968;37(6):1024–9.

    CAS  Google Scholar 

  38. Tomas MJE, Simon-Pujol MV, Congregado F, Suarez-Fermandez G. Methods II a thesis antagonism of soil microorganisms toward fungal spore germination. J Soil Biology and Biochemistry. 1980;12:197–8.

    Article  Google Scholar 

  39. Tietz NW. Fundamentals of clinical chemistry. Philadelphia: W.B. Saunders Company; 1987. p. 563.

    Google Scholar 

  40. Kaur S, Vohra RM, Kapoor M, Khalial Q, Hoondal GS. Enhanced production and characterization of a highly thermostable alkaline protease from Bacillus sp. P-2. W. J Microbial Biotechnol. 2001;17:125–9.

  41. Inouye Y, Taguchi K, Fuji A, Ishimaru K, Nakamura S, Nomi R. Purification and characterization of extracellular 3ß-hydroxysteroid oxidase produced by Streptoverticillium cholesterolicum. Chem Pharm Bull. 1982;30:951–8.

    Article  CAS  Google Scholar 

  42. Lowry OH, Rosebrough NT, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem. 1951;139:265–75.

    Google Scholar 

  43. Laemmli VK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970;227:680–5.

    Article  CAS  PubMed  Google Scholar 

  44. Studier FW. Analysis of bacteriophage T7 early RNAs and proteins of stabgels. J Mol Biol. 1973;79:237–48.

    Article  CAS  PubMed  Google Scholar 

  45. Duncan DB. Multiple range and multiple (F) test. Biometrics. 1955;11:1–45.

    Article  Google Scholar 

  46. Dytham C. Choosing and statistics: Abiologists guide. London, UK: Blackwell science Ltd.; 1999. p. 147.

    Google Scholar 

  47. Gay AV, Sobouti R. Cholesterol is accumulated by mycobacteria but its degradation is limited to non-pathogenic fast-growing mycobacteria. J Microbiol. 2000;46(9):826–31.

    Google Scholar 

  48. Suzuki K, Bruce WR, Baptista J, Furrer R, Vaughan DJ, Krepinsky JJ. Formation of cholest-4-en-3-one by intestinal bacteria and its biological effect. Cancer Lett. 1986;33:307.

    Article  CAS  PubMed  Google Scholar 

  49. Chang YC, Chou CC. Growth and production of cholesterol oxidase by alginate-immobilized cells of Rhodococcus equi No. 23. J Biotechnol and Appl Biochem. 2002;35(2):69–74.

    Article  CAS  Google Scholar 

  50. Sabry AA. Decomposition of cholesterol by some organisms isolated from certain Egyption soils. Cairo, Egypt: M.Sc. Thesis. Bot. and Microbiol. Dept. Al-Azhar University; 1994.

    Google Scholar 

  51. Murray PR, Baron EJ, Pfaller MA, Tenover FC, Yolken RH. Manual of clinical microbiology. sixthth ed. Washington, D .C: ASM press; 1995. p. 308–14. ISBN 1-55581-086-1.

    Google Scholar 

  52. Leland AU. Microbial enzymes. In: Industrial Microbiology. 7th ed. USA: Mc Graw-Hill Bool Company; 1976. p. 128–64.

    Google Scholar 

  53. Gruber W, Bergmeyer HU, Nelbock- Hochstetter M, Beaucamp K, Holz G, Gramsall J. Patent US4144129 - Cultures, solvent extraction, 1979,

  54. Ahn KW, Sampson NS. Cholesterol oxidase senses changes in lipid bilayer structure. Department of Chemistry, State University of New York, USA. J Biochemistry. 2004;43(3):827–36.

    Article  CAS  Google Scholar 

  55. Tietz NW. Fundamentals of clinical chemistry. Company: Philadelphia W. B. Saunders; 1994. p. 1067–8.

    Google Scholar 

  56. Lario PI, Vrielink A. Atomic resolution density maps reveal secondary structure dependent differences in electronic distribution. Department of Molecular Cellular and Developmental Biology, University of California, USA. 2003;125(42):12787–94.

    CAS  Google Scholar 

  57. Praveen V, Srivastava A, Tripathi CKM. Purification and characterization of the enzyme cholesterol oxidase from a new isolate of Streptomyces sp. J Basic Microbiol. 2011;165(5-6):1414–26.

    CAS  Google Scholar 

  58. Ammar MS, Lashin IF, Abdullah HE. Cholesterol decomposing microorganisms isolated from some human skin microflora. Egypt J Microbiol. 1990;25(1):9–17.

    Google Scholar 

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The authors would like to extend their sincere appreciation to the Deanship of Scientific Research at King Saud University for funding this research through Research Group Project No. RG-1435- 016.

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Correspondence to Hany M. Yehia, Wesam A. Hassanein or Shimaa M. Ibraheim.

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WAH and SMI designed the experiments, analyzed the data, and drafted the manuscript. HMY and SMI carried out the experiments. All authors read and approved the final manuscript.

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Yehia, H.M., Hassanein, W.A. & Ibraheim, S.M. Purification and characterisation of the extracellular cholesterol oxidase enzyme from Enterococcus hirae . BMC Microbiol 15, 178 (2015).

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