Mini Review - (2022) Volume 4, Issue 2
Pseudomonas aeruginosa in Industries
Nida Tabassum Khan*
*Correspondence:
Nida Tabassum Khan, Department of Biotechnology, Faculty of Life Sciences & Informatics, Baluchistan University of Infor, Engineering and Management Sciences, Takatu Campus, Airport Road, Quetta, Baluchistan,
Pakistan,
Email:
Author info »
Abstract
Pseudomonas aeruginosa is a Gram-negative is a bacterium of the Pseudomonadaceae family (an individual from the Gamma proteobacteria). It is ordinarily isolated from soil and water as well as in plants and humans. Pseudomonas microscopic organisms are accepted to be a very rare example of genuine microbes for plants. Critically, Pseudomonas aeruginosa are known as opportunistic human pathogens however numerous industrial products including Rhamnolipids, Vanillin etc. are also synthesize by these species.
Keywords
Rhamnolipids • Vanillin • Bioremediation • Opportunistic • Monoflagellated
Introduction
A monoflagellated gram-negative rod-shaped bacterium that is known to human as an opportunistic pathogen [1]. Pseudomonas aeruginosa is of great clinical significance since it is a multidrug resistant microbe perceived for its presence in any sort of environment [2]. Pseudomonas aeruginosa rhamnolipids, glycolipidic surface-dynamic molecules which have potential biotechnological applications [3, 4]. Rhamnolipids are produced by Pseudomonas aeruginosa in biosynthetic pathway and exhibits metabolic connections with various bacterial secretes including alginate, lipopolysaccharide, polyhydroxyalkanoates, and 4-Hydroxy2-Alkylquinolines (HAQs) [5, 6]. Pseudomonas aeruginosa secretes an exopolysaccharide called alginate that provide protection to the microbes in difficult environmental conditions and furthermore improves its adhesion to strong surfaces [7, 8]. Alginate biosynthetic gene is incited upon connection to the base surface and this prompt expanded alginate synthesis [9]. Subsequently, biofilms which are beneficial to the endurance and development of the microorganisms is formed [10, 11]. Moreover, versatile anti-toxin resistance of Pseudomonas aeruginosa incorporates biofilm-interceded resistance and development of multidrugtolerant persistent cells for recalcitrance and relapse of infections [12, 13]. Pseudomonas aeruginosa plays an important in biotechnology-based applications some of which are as follows:
It is broadly utilized as a model organism because of its wide metabolic adaptability that it is generally used to study biotechnological applications [14].
Pseudomonas aeruginosa is utilized for the investigation of antibiotic resistance and pathogenesis [15]. It produces an enormous number of compounds with bacteriostatic or bacteriocidic properties, these compounds are significant in the control of various Multi Drug Resistance (MDR) [16, 17]. For example, carbapenems producing Klebsiella pneumoniae and methicillin resistant Staphylococcus aureus [18].
• Pseudomonas aeruginosa plays a significant role in the bioremediation of heavy metals like lead, copper, cadmium and chromium since metals are straightforwardly and by implication engaged with all parts of microbial development [19]. Different Pseudomonas aeruginosa strains can biodegrade countless toxic compounds that are recalcitrant to other bacterial species, subsequently delivering auxiliary metabolites and biopolymers, making these strains helpful in medication and industries [20, 21].
• Pseudomonas aeruginosa has valuable purposes in different modern applications and industrial sectors as these bacteria incorporates the ability to biodegrade waste, petroleum processing derived from plants, agribusiness, mash and paper, mining etc. [22, 23]. They can also be used in commercial and household drain cleaners and degreasers, septic tank additives, general cleaning products, and odour control products [24, 25].
• Various strain of Pseudomonas aeruginosa has been recognized as micro factories for the biosynthesis of useful substances [26]. Some of these products are given below:
• Vanillin: Recent studies reported that Pseudomonas aeruginosa ISPC2 strain produces vanillin through microbial biotransformation utilizing isoeugenol as a precursor molecule [27].
• Rhamnolipids: It has been shown that rhamnolipids can be investigated to control and disrupt the formation of bacterial biofilms mainly of food-borne microbes [28].
• Protease: Proteolytic enzymes are to a great extent tracked down in every single living creature and are vital for the development of cells [29]. Pseudomonas aeruginosa releases extracellular protease utilizing maltose as a significant carbon source [30].
• Lipase: Pseudomonas aeruginosa are one of the most amazing producers of lipase catalyst which have shown extraordinary potential concerning their application in various industrial enterprises [31].
• Biopigments: The different kinds of pigments produced by Pseudomonas aeruginosa are to a great extent classed under the synthetic name of phenazines [32]. Phenazine compounds are of good biotechnological value [33].
Conclusion
Thus, Pseudomonas aeruginosa have been widely implicated as clinical pathogens but it is also offering numerous biotechnological benefits.
References
- Wu, W., et al., “Pseudomonas aeruginosa.” In Mol. med. microbiol. (2015): 753-767. Academic Press.
[Google Scholar] [cross ref]
- Strateva, T., & Yordanov, D., “Pseudomonas aeruginosa–a phenomenon of bacterial resistance.” J. med. microbiol. 58.9(2009): 1133-1148.
[Google Scholar] [Cross ref]
- Jarvis, F. G., & Johnson, M. J., “A glyco-lipide produced by Pseudomonas aeruginosa.” J. Am. Chem. Soc. 71.12(1949): 4124-4126.
[Google Scholar] [Cross ref]
- Kerr, K., & Snelling, A., “Pseudomonas aeruginosa: a formidable and ever-present adversary.” J. Hosp. Infect., 73.4(2009): 338-344.
[Google Scholar] [Cross ref]
- Mata-Sandoval, J., et al., “High-performance liquid chromatography method for the characterization of rhamnolipid mixtures produced by Pseudomonas aeruginosa UG2 on corn oil.” J. Chromatogr. A. 864.2(1999), 211-220.
[Google Scholar] [Cross ref]
- Rahman, K., et al.,“Rhamnolipid biosurfactant production by strains of Pseudomonas aeruginosa using low‐cost raw materials.” Biotechnol. Prog. 18.6(2002): 1277-1281.
[Google Scholar] [Cross ref]
- Stapper, A., et al., “Alginate production affects Pseudomonas aeruginosa biofilm development and architecture, but is not essential for biofilm formation.” J. med. microbiol. 53.7(2004), 679-690.
[Google Scholar] [Cross ref]
- Fyfe, J. A., & Govan, J. R. “Alginate synthesis in mucoid Pseudomonas aeruginosa: a chromosomal locus involved in control.” Microbiology 119.2(1980): 443-450.
[Google Scholar] [Cross ref]
- Boyd, A., & Chakrabarty, A. “Pseudomonas aeruginosa biofilms: role of the alginate exopolysaccharide.” J. ind. microbiol. biotechnol. 15.3(1995), 162-168.
[Google Scholar] [Cross ref]
- Nagino, K., & Kobayashi, H., “Influence of macrolides on mucoid alginate biosynthetic enzyme from Pseudomonas aeruginosa.” Clin. Microbiol. Infect. 3.4(1997): 432-439.
[Google Scholar] [Cross ref]
- Ghafoor, A., et al., “Role of exopolysaccharides in Pseudomonas aeruginosa biofilm formation and architecture.” Appl. environ. microbiol. 77.15(2011): 5238-5246.
[Google Scholar] [Cross ref]
- Valentine, M. et al., “Generation of a highly attenuated strain of Pseudomonas aeruginosa for commercial production of alginate.” Microb. biotechnol 13.1(2020): 162-175.
[Google Scholar] [Cross ref]
- Franklin, M., et al., “Biosynthesis of the Pseudomonas aeruginosa extracellular polysaccharides, alginate Pel, and Psl.” Front. microbiol.2.167(2011)
[Google Scholar] [Cross ref]
- Breidenstein, E., et al., “Pseudomonas aeruginosa: all roads lead to resistance.” Trends microbial. 19.8(2011): 419-426.
[Google Scholar] [Cross ref]
- Aloush, V., et al., “Multidrug-resistant Pseudomonas aeruginosa: risk factors and clinical impact.” Antimicrob. agents chemother. 50.1(2006), 43-48.
[Google Scholar] [Cross ref]
- Bonomo, R., & Szabo, D., “Mechanisms of multidrug resistance in Acinetobacter species and Pseudomonas aeruginosa.” Clin. infect. dis. 43.Supplement_2 (2006): S49-S56.
[Google Scholar] [Cross ref]
- Porras Gomez, M., et al., “Overview of multidrug-resistant Pseudomonas aeruginosa and novel therapeutic approaches.” J. Biomater. Nanobiotechnology 3(2012): 519-527.
[Google Scholar] [Cross ref]
- Lomovskaya, O., et al., “Identification and characterization of inhibitors of multidrug resistance efflux pumps in Pseudomonas aeruginosa: novel agents for combination therapy.” Antimicrob. agents chemother. 45.1(2001), 105-116.
[Google Scholar] [Cross ref]
- Chellaiah, E. R. “Cadmium (heavy metals) bioremediation by Pseudomonas aeruginosa: a minireview.” Appl. water sci. 8.6 (2018), 1-10.
[Google Scholar] [Cross ref]
- Karamalidis, A., et al., “Laboratory scale bioremediation of petroleum-contaminated soil by indigenous microorganisms and added Pseudomonas aeruginosa strain Spet.” Bioresour. technol. 101.16(2010), 6545-6552.
[Google Scholar] [Cross ref]
- O'Brien, S., et al., “Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa.” Proc. R. Soc. B: Biol. Sci. 281.1787(2014): 20140858.
[Google Scholar] [Cross ref]
- Thavasi, R., et al., “Biosurfactant production by Pseudomonas aeruginosa from renewable resources.” Indian j. microbiol. 51.1(2011): 30-36.
[Google Scholar] [Cross ref]
- Lakshmanan, R., et al., “Identification and characterization of Pseudomonas aeruginosa derived bacteriocin for industrial applications.” Int. J. Biol. Macromol. 165 (2020): 2412-2418.
[Google Scholar] [Cross ref]
- Zhao, F., et al., “Enhanced production of mono-rhamnolipid in Pseudomonas aeruginosa and application potential in agriculture and petroleum industry.” Bioresour. Technol., 323(2021): 124605.
[Google Scholar] [Cross ref]
- Perfumo, A., et al., “Rhamnolipid production by a novel thermophilic hydrocarbon-degrading Pseudomonas aeruginosa AP02-1.” Appl. microbiol. biotechnol. 72.1(2006): 132-138.
[Google Scholar] [Cross ref]
- Chandrashekar, V., et al., “Assessment of acrylamide degradation potential of Pseudomonas aeruginosa BAC-6 isolated from industrial effluent.” Appl. biochem. biotechnol. 173.5(2014): 1135-1144.
[Google Scholar] [Cross ref]
- Ashengroph, M., et al., “Use of growing cells of Pseudomonas aeruginosa for synthesis of the natural vanillin via conversion of isoeugenol.” Iran. J. Pharm. Res.: IJPR 10.4(2011); 749.
[Google Scholar] [Cross ref]
- Soberon-Chavez, et al., “Production of rhamnolipids by Pseudomonas aeruginosa.” Appl. microbiol. biotechnol. 68.6(2005): 718-725.
[Google Scholar] [Cross ref]
- Engel, L. et al., “Protease IV, a unique extracellular protease and virulence factor from Pseudomonas aeruginosa.” J. Biol. Chem. 273.27(1998): 16792-16797.
[Google Scholar] [Cross ref]
- Sokol, P., et al., “A more sensitive plate assay for detection of protease production by Pseudomonas aeruginosa.” J. clin. microbiol. 9.4(1979): 538-540.
[Google Scholar] [Cross ref]
- Kathiravan, T., et al., “Studies on nutritional requirements of Pseudomonas aeruginosa for lipase production.” Adv Appl Sci Res 3.19(2012): 591-598.
[Google Scholar] [Cross ref]
- Wilson, R., et al., “Measurement of Pseudomonas aeruginosa phenazine pigments in sputum and assessment of their contribution to sputum sol toxicity for respiratory epithelium.” Infect. immun. 56.9(1988): 2515-2517.
[Google Scholar] [Cross ref]
- Chang, P., & Blackwood, A., “Simultaneous production of three phenazine pigments by Pseudomonas aeruginosa Mac 436.” Can. j. Microbiol. 15.5(1969): 439-444.
[Google Scholar] [Cross ref]
Author Info
Nida Tabassum Khan*
Department of Biotechnology, Faculty of Life Sciences & Informatics, Baluchistan University of Infor, Engineering and Management Sciences, Takatu Campus, Airport Road, Quetta, Baluchistan, Pakistan
Citation: Khan NT. Pseudomonas aeruginosa in Industries. J Pharmac Sci Drug Dev. 2022, 4(2), 001-002
Received: 01-Aug-2022, Manuscript No. JPSDD-22-70865;
Editor assigned: 03-Aug-2022, Pre QC No. JPSDD-22-70865 (PQ);
Reviewed: 08-Aug-2022, QC No. JPSDD-22-70865 (Q);
Revised: 10-Aug-2022, Manuscript No. JPSDD-22-70865 (R);
Published:
20-Aug-2022, DOI: 10.37532/jpsdd.22.4.2.1-2
Copyright: © 2022 Khan NT. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.