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Memórias do Instituto Oswaldo Cruz

Print version ISSN 0074-0276On-line version ISSN 1678-8060

Mem. Inst. Oswaldo Cruz vol.91 no.6 Rio de Janeiro Nov./Dec. 1996

http://dx.doi.org/10.1590/S0074-02761996000600020 

BIOCHEMISTRY

 

Detection of extracellular proteases from microorganisms on agar plates

 

 

Alane Beatriz VermelhoI, +; Maria Nazareth Leal MeirellesII; Andréa LopesI; Simone Dias Gonçalves PetinateI; André Adriano ChaiaI; Marta Helena BranquinhaI

IDepartamento de Microbiologia Geral, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, Cidade Universitária, Ilha do Fundão, 21944-970 Rio de Janeiro, RJ, Brasil
IILaboratório de Ultraestrutura e Biologia Celular, Instituto Oswaldo Cruz, Av. Brasil 4365, 21045-900 Rio de Janeiro, RJ, Brasil

 

 


ABSTRACT

We present herein an improved assay for detecting the presence of extracellular proteases from microorganisms on agar plates. Using different substrates (gelatin, BSA, hemoglobin) incorporated into the agar and varying the culture medium composition, we were able to detect proteolytic activities from Pseudomonas aeruginosa, Micrococcus luteus and Serratia marcescens as well as the influence that these components displayed in the expression of these enzymes. For all microorganisms tested we found that in agar-BHI or yeast extract medium containing gelatin the sensitivity of proteinase detection was considerably greater than in BSA-agar or hemoglobin-agar. However, when BSA or hemoglobin were added to the culture medium, there was an increase in growth along with a marked reduction in the amount of proteinase production. In the case of M. luteus the incorporation of glycerol in BHI or yeast extract gelatin-agar induced protease liberation. Our results indicate that the technique described here is of value for detecting extracellular proteases directly in the culture medium, by means of a qualitative assay, simple, inexpensive, straight forward method to assess the presence of the proteolytic activity of a given microorganism colony with great freedom in substrate selection.

Key words: protease - detection - microorganism


 

 

Proteases play a crucial role in numerous pathologic processes. Arthritis, tumor invasion and metastasis, infections and a number of degenerative diseases have been linked with the involvement of one or more proteolytic enzymes (Brown 1994). Microbial proteases have been proposed as virulence factors in a variety of diseases caused by microorganisms. The virulence of Pseudomonas aeruginosa is multifactorial, but it is partly determined by exoproducts such as alkaline protease and elastase, which are responsible for the damage of tissues by degrading elastin, collagen and proteoglycans. These enzymes have been also shown to degrade proteins that function in host defense in vivo (Sakata et al. 1993).

In bacteria, serine- and metalloproteases are the principal classes of proteases found in several species such as Bacillus subtilis, B. amyloliquefaciens, Pseudomonas sp., Lysobacter enzymogenes and Escherichia coli (Fujishige et al. 1992). Identification and characterization of microbial proteases are prerequisites for understanding their role in the pathogenesis of infectious diseases as well as to improve their application in biotechnology. For this aim, rapid and sensitive techniques for the detection and characterization of microbial proteases are highly desirable (Lantz & Ciborowski 1994).

Proteases are also one of the highest value commercial enzymes. They find application in the food, pharmaceutic and detergent industries and are important tools in studying the structure of proteins and polypeptides (Bhosale et al. 1995).

The present study describes a qualitative method for detection of extracellular proteases on agar plates and the proper culture medium for their production.

 

MATERIALS AND METHODS

Microorganisms - The microorganisms employed in this study - P. aeruginosa ATCC 19429, Serratia marcescens isolated from clinical material at Hospital Clementino Fraga Filho, UFRJ, RJ and Micrococcus luteus isolated from skin - were maintained either in 5% (w/v) brain heart agar (Merck) (medium A) or in 2% (w/v) sucrose (Merck), 0.5% (w/v) yeast extract (Biobrás), 2% (w/v) peptone (BBL), 2% (w/v) KCl (Reagen) and 1.5% (w/v) agar (Difco) (medium B).

Detection media - The detection media were the same described above, supplemented and autoclaved with 1% (w/v) gelatin (Merck). The medium with 1% (w/v) bovine serum albumin (BSA - Sigma) was made from a stock solution containing 1g BSA made up to 5 ml with water. This solution was sterilized using 0.22 µm filter membranes and added to culture medium at 45°C. The medium with 1% hemoglobin (BBL) was made from a stock solution containing 1 g hemoglobin made up to 50 ml with water. This solution was autoclaved, cooled to approximately 50°C and an equal proportion to sterile medium A or B was added. Each medium was adjusted to pH 7.0.

Twenty ml of culture media A or B (supplemented with gelatin, BSA or hemoglobin) were then poured per plate and allowed to harden. A loopful of the culture growth was placed in the center of the agar plates. After inoculation, the plates were incubated at 37°C and observed daily for ten days. For BSA and gelatin, extracellular protease detection was done after staining with 0.1% amido black in methanol-acetic acid-water 30:10:60 (v/v/v) for 1 hr at 28°C. Coomassie blue (0.25%, w/v) in methanol-acetic acid-water 5:1:4 (v/v/v) could also be used, although destaining may require the use of methanol and acetic acid. Regions of enzyme activity were detected as clear areas, indicating that hydrolysis of the substrates had occurred. For hemoglobin, the extracellular protease detection was directly observed in agar plates as well as with amido black and/or Coomassie blue. The proteinase activity was scored as grade - when no visible halo was present, grade + when visible proteolysis was limited to 1-2 mm around the colony and grade ++ when the zone of proteolysis was more than 2 mm from the margin of the colony.

Influence of the medium composition (carbon source) on the expression of extracellular proteases by M. luteus - M. luteus was inoculated in four different culture media, using 1% (w/v) gelatin as substrate por proteolytic detection: medium A; medium B; medium C was the same as medium B with sucrose being replaced by 2% (w/v) glycerol; medium D with the following composition: 2% (w/v) glycerol (Reagen), 0.45% (w/v) peptone, 0.2% (w/v) K2HPO4, 0.03% (w/v) KCl, 0.05% (w/v) MgSO4 and 1.5% agar.

 

RESULTS

Effect of protein substrates and culture media in extracellular protease production - M. luteus, S. marcescens and P. aeruginosa were screened for extracellular proteinase production by inoculation onto BHI- or yeast extract-agar medium supplemented with gelatin, BSA or hemoglobin as substrate. Protease activity was detected 24 hr post-inoculation. Clear halos increased until the fifth day, and remained constant during ten days. All microorganisms tested hydrolysed preferentially gelatin incorporated in BHI or yeast extract. When the culture medium was supplemented with BSA or hemoglobin, the microorganisms caused proteolysis beyond the hinge of colonies or just a slight hydrolysis (Table).

M. luteus hydrolysed gelatin in BHI-agar, but exhibited no zones of clearing in yeast extract-agar (Fig. 1). This bacterium did not hydrolyse BSA in both culture media (Fig. 2), but utilize hemoglobin producing clear zones only around the colonies (Fig. 3).

P. aeruginosa showed great clear halos in gelatin-media (Fig. 1). However, when inoculated in BSA- and hemoglobin-agar in both media, a very low production of extracellular proteases was detected, although the growth of the colonies was increased (Figs 2, 3).

The microorganism S. marcescens also hydrolysed preferentially gelatin (Fig. 1) but did not produce detectable proteolytic enzymes in hemoglobin medium, which was the best medium for the growth of this bacterium (not shown). It also yields low proteolytic activity in BSA-containing media (Fig. 2).

Effect of the carbon source on the expression of extracellular proteases by M. luteus - Yeast extract supplemented with sucrose inhibited the protease secretion by M. luteus. Using the same culture medium but replacing sucrose by glycerol as carbon source a marked increase in protease production was observed. The same effect was observed when the glycerol-containing medium D was used (Fig. 3).

 

DISCUSSION

This study has shown that protein substrates can influence markedly the production of extracellular proteases by bacteria such as P. aeruginosa, S. marcescens and M. luteus. There was also evidence which indicated that the composition of the medium can modify the influence of a substrate on protease production.

The most proeminent proteolytic activity was found in P. aeruginosa, which hydrolysed gelatin, BSA and hemoglobin. It is known that P. aeruginosa secrete two metalloendopeptidases: the elastase, now called pseudolysin (EC 3.4.24.26) and an alkaline protease (Morihara 1995). S. marcescens hydrolysed preferentially gelatin and did not utilize hemoglobin as protein substrate. This microorganism produces two metalloproteinases with Mr of 56 kDa and 60 kDa, being the 56 kDa the proeminent enzyme and a 73 kDa thiol-dependent proteinase (Maeda & Morihara 1995). The bacterium M. luteus did not use BSA as substrate on agar plates and produced a weak proteolytic activity when hemoglobin was incorporated in the nutrient agar plates. The best substrate for protease production for M. luteus was gelatin. Preliminary studies of our laboratory showed that it produces a high-molecular weight serine-protease (Petinate et al. 1995).

Differences in the ability to utilize gelatin, hemoglobin and BSA may be due to differences in the substrate specificities of the enzyme produced (de Giorgi et al. 1985, Ponsare et al. 1985) or may be the consequence of parameters known to affect extracellular proteinase production, such as pH, medium composition and temperature. Gelatin, a type 1 collagen, was the most effective protease-inducing substrate, followed by hemoglobin. It is possible that gelatin, as a high molecular weight protein, induces an increase in the protease production to degrade the substrate to an available form for the microorganism.

It has been described that addition of glucose to various media increase the growth of P. aeruginosa but there was a marked reduction in the amount of proteinase production. These results suggest that protease production by P. aeruginosa was subject to catabolite repression by glucose when peptones were the source of nitrogen (Juffs 1976). The composition of the two culture media used in our study (BHI or yeast extract) did not modify the degradation of the substrates, except by M. luteus, in which no protease was detected in yeast extract-gelatin and a strong activity was found in BHI-gelatin. Our results showed that M. luteus did not produce protease when sucrose was used as carbon source. The enzyme production is induced when glycerol was used as carbon source (culture media C and D). These results suggest the possibility that sucrose could exert the same effect in catabolite repression than glucose in P. aeruginosa.

It has been described methods to assay proteolytic activity involving colorimetric analysis (Rinderknecht et al. 1968), the use of fluorogenic substrate (Rust et al. 1994), zymographic techniques (Lantz & Ciborowski 1994) and incorporation of different substrates in nutrient agar plates, such as skim milk (Sacherer et al. 1994), BSA (Rüchel et al. 1982), casein (Ahearn et al. 1968) and elastin (Rust et al. 1994).

In this work, gelatin, BSA and hemoglobin have been used as enzyme substrate. A wide range of methods are available for detecting proteases using gelatin as substrate (Grubb 1994). These methods as with other protease assays are based on the hydrolysis of substrate for detection of gelatinase-like proteases and have been used in several methods for biochemical studies (Branquinha et al. 1996) and in clinical laboratory for identification of bacteria (MacFaddin 1980). BSA, a smaller molecule, is also frequently used incorporated in SDS-PAGE (Kelleher & Juliano 1984) or in radial diffusion in agar gel (Wikström et al. 1981). Denatured hemoglobin is routinely used in assay systems for detecting proteolytic activity (Anson 1939) and also incorporated in SDS-PAGE (Andary & Dabich 1974).

The technique we describe is of value for detecting extracellular proteases directly in the culture medium. The use of gelatin in the culture medium provided us a qualitative assay, a simple, inexpensive, straight forward method to assess the presence of proteolytic activity of a given colony. In addition, the method allows greater freedom in substrate selection since low-(BSA, hemoglobin) or high-molecular weight (gelatin) proteins could be used. This method, for instance, allows to verify in an initial screening whether the bacteria secrete extracellular proteases and the best culture medium composition to detect this production. In summary, the simplicity of this method is its greatest advantage, although it cannot be used to quantitate degradation.

 

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Received 31 October 1995
Accepted 25 July 1996
This work was supported by CNPq (PADCT/RHAE), CEPG/UFRJ, FINEP, FUJB and FIOCRUZ.

 

 

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