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Serratia marcescens on MacConkey agar.

Serratia marcescens on MacConkey agar.

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In order to induce rapid division of the bacterial cells and to stimulate the specific metabolic products of these cells, the researcher prefers to use natural culture medium as an alternative to the synthetic medium. This study aimed to stimulate the production of the prodigiosin (red pigment) in the bacterium Serratia marcescens that was grown on...

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Context 1
... cultural characteristics of S. marcescens colonies were red on nutrient agar and late lactose fermenter on MacConkey agar ( fig. 1). Then were carried out the staining technique under a microscope. The definitive identification of Serratia marcescens was done using the VITEK® 2 GN ID ...
Context 2
... of starch molecules with the proteolytic enzymes; because of the containment the legumes to carbohydrates and proteins According to Basam et al. (2019), Yang et al. (2012), Kamble and Hiwarale (2012). While the color of prodigiosin that produced from Isolates Serratia marcescens of water samples was orange on the solid medium of legumes mixture (fig. ...
Context 3
... oil, palm oil & olive oil as well as using the sunflower or castor seeds because it's considered as an essential source of carbon and nitrogen that bacteria need to stimulate prodigiosin (Pankaj et al., 2015;Chidambaram and Perumalsamy, 2009). But in this study, we proved it is possible to stimulate the pigment by a non-fatty or oily substrates ( fig. ...
Context 4
... cultural characteristics of S. marcescens colonies were red on nutrient agar and late lactose fermenter on MacConkey agar ( fig. 1). Then were carried out the staining technique under a microscope. The definitive identification of Serratia marcescens was done using the VITEK® 2 GN ID ...
Context 5
... of starch molecules with the proteolytic enzymes; because of the containment the legumes to carbohydrates and proteins According to Basam et al. (2019), Yang et al. (2012), Kamble and Hiwarale (2012). While the color of prodigiosin that produced from Isolates Serratia marcescens of water samples was orange on the solid medium of legumes mixture (fig. ...
Context 6
... oil, palm oil & olive oil as well as using the sunflower or castor seeds because it's considered as an essential source of carbon and nitrogen that bacteria need to stimulate prodigiosin (Pankaj et al., 2015;Chidambaram and Perumalsamy, 2009). But in this study, we proved it is possible to stimulate the pigment by a non-fatty or oily substrates ( fig. ...

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Citations

... This finding suggests that these products may be utilised to generate enzymes, significantly lowering the cost of culture media. Combinations of legumes were utilised by Mohammed et al. (2020) to create a media that encouraged Serratia marcescens to produce prodigiosin pigments. White beans, fava beans, mung beans, peas, chickpeas, black beans, and lentil powders were used to make the medium. ...
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... Legumes have also been manipulated for the development of new media (Ravimannan et al., 2014;Uthayasooriyan et al., 2016;Shareef, 2019;Mohammed et al., 2020). Legumes are food crops belonging to the Leguminosae family. ...
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... Serratia marcescens which is additionally known as "Chromobacterium Prodigiosum" is a gramnegative rod shape bacterium belongs to the family of Enterobacteriaceae (Hejazi & Falkiner, 1997). It is an opportunistic, motile, non-spore forming, prodigiosin (red pigment) producing bacteria which grows on both aerobic and anaerobic conditions (Mohammed et al., 2020) at room temperature and at 37 0 C. In the late 1960s, Serratia marcescens was isolated from the intestine of silk worm called Bombyx mori L. (Devi et al., 2013). ...
Thesis
Proteolytic enzymes are capable of hydrolyzing the peptide bonds amid amino acid residues of the protein. Serratia marcescens is a gram-negative bacterium belonging to the family of Enterobacteriaceae. Serratia peptidase is a well-known proteolytic enzyme produced by Serratia marcescens (Strain E-15). The objectives of this study were to extract, purify and characterize the bacterial peptidase produced by Serratia marcescens. The isolate was identified by morphological and biochemical characteristics. Screening of protease was conducted by using skim milk and gelatin agar. Protease assay, Bradford assay, and ammonium sulfate precipitation were also carried out. Characterization was implemented with different concentrations of enzyme, EDTA as an inhibitor, different temperatures, and pH. The enzyme was purified by gel filtration chromatography and the molecular weight was analyzed by SDS-PAGE. Protease assay showed the activity of crude enzyme as 1.572 U/ml and 0.46 U/ml of precipitated proteins. Bradford assay exhibited the total protein concentration as 0.0853 mg/ml. Characterization indicates that the enzyme activity was increased up to 100 μl with 1.03 U/ml, and the enzyme was inhibited by 83% by using EDTA with an optimum temperature of 45°C and pH of 8.0. The molecular weight of the enzyme was found to be approximately 50 kDa by SDS-PAGE. It was concluded that the purified enzyme is serratia peptidase. Keywords: Proteolytic enzymes, Serratia marcescens, Serratia peptidase.
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