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Increasing Antibiotic Yield for the Method of Dispersed Growth of Streptomyces in Liquid Culture

2404 words (10 pages) Essay in Biology

08/02/20 Biology Reference this

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Introduction

Streptomyces is a genus of filamentous bacteria. It is in the family Streptomycetaceae, they include over 500 species, which occur in both soil and water (Hodgson, 2000). A lot of the species are important in the process of decomposition of organic matter in soil, these species contribute to the earthy odour of soil and also of decaying leaves, it also contributes to the fertility of soil (Hodgson, 2000). Some of the species are notable for their production of broad-spectrum antibiotics (Blaskovich et al., 2017), chemicals that the bacteria are able to naturally produce to kill or are able to inhibit the growth certain microorganisms (Hodgson, 2000). The antibiotic producers include: S. aureofaciens (yielding chlortetracycline), S. rimosis (oxytetracycline; see tetracycline), S. griseus (streptomycin), S. erythraeus (erythromycin), and S. venezuelae (chloramphenicol) (Hodgson, 2000). Streptomyces is categorised as gram-positive aerobic bacteria and they are of a complex form (Hodgson, 2000).

Streptomyces is one of the most vital group of industrial microorganisms as a producer of bioactive compounds and are the main bacteria used for the production of antibiotics (Blaskovich et al., 2017).

Within liquid culture, Streptomyces grows in the form of a pellet (Vecht-Lifshitz et al., 1990). The pellets will have limitations due to mass transfer, this produces a solute gradient through the sphere (Feeney, 2015). In the centre of the pellets the cells will be nutrient limited (Hobbs et al., 1989). This growth method means that problems arise for the physiology of the microbial (Feeney, 2015). Due to cells containing Streptomyces to have a variety of physiological states. It isn’t clear whether dispersed growth happens at a phenotypic level or a genotypic level (Hobbs et al., 1989). Whichever one it is the instability genetically means that there’s a very high chance that changes will happen if there is prolonged continuous growth (Hobbs et al., 1989). Pellet formation is not exclusive to Streptomyces, its seen in liquid cultures of fungi (Vecht-Lifshitz, Magdassi and Braun, 1990). In a number of fungal species, the incorporation of high weight molecular weight polyanions into the growth media has solved the problem of pellet formation in liquid cultures (Hobbs et al., 1989. The polymeric compounds are thought to act by inducing electrostatic repulsion between the spores or the cells, this prevents initial aggregation of spores in the inocula as well as clumping of mycelia that is in the growth culture (Guthrie et al., 1998).

The production of oxytetracycline increased after immobilization of Streptomyces rimosus cells in calcium alginate gels in comparison with free cells in a study by Enshasy et al. (1996). Studies have shown that the use of immobilized cells that adhered on glass wool for both rifamycins and oxytetracycline production for 5 repeated batches had been looked in to (Feeney, 2015). The aim of the paper by Enshasy et al. (1996) was to describe the optimal conditions for repeated batch production of oxytetracycline by immobilized cells, and the productivity of immobilized cells for 10 repeated batches in comparison with free cells (Enshasy et al., 1996).

The use of culture systems where plant cells are immobilized on a stationary support is acknowledged as a way by which the cell environment can be manipulated, and therefore the yields of specific secondary metabolites increased the cells suspended in liquid (Dervakos and Webb, 1991). So that microbial contamination is kept to a minimum, the number of steps in the immobilised procedure have to be kept to a minimum (Doleyres and Lacroix, 2005).

Using immobilised cells rather than free cells has many advantages such as enhanced biological stability, high biomass concentration, improved mass transfer, advantageous partition effects Increased product yields, increased product stability, integration with downstream processing Advantages due to cell proximity Increased reaction selectivity and versatility in the selection of the reactor (Lindsey et al., 1983). There are a number of different methods that has been used for immobilising bacteria, these include physical entrapment in polymeric networks, attachment / adsorption to a preformed carrier, membrane entrapment and microencapsulation (Doleyres and Lacroix, 2005).

Immobilisation offer a number of advantages for biomass and metabolite production (Leenen et al., 1996) this is compared to free-cell systems which include high cell density, reuse of biocatalysts, improved resistance to contamination and bacteriophage attack, enhancement of plasmid stability, prevention from washing-out during continuous cultures, and physical and chemical protection of cells (Lindsey et al., 1983). Immobilised cells have the advantage of being alive but not necessarily replicating. This is the perfect state for antibiotic producing cells (Leenen et al., 1996). living, non-reproducing cells, retained by a membrane or fixed to a carrier, are used (Wandrey, 1996).

Biotechnological processes based on immobilized whole cells have developed quickly over the last few decades, mainly using viable, metabolically active microorganisms (Chaumeil, 2015). Natural immobilized cell (IC) structures, ie, biofilms, are being increasingly investigated at the cellular level owing to their importance for human health and various areas of industrial and environmental relevance (Junter and Jouenne, 2017).

A number of immobilisation techniques have been described over the last 40 years, in mainly in books and journals (Kandimalla, 2008). Immobilising cell systems can be separated into either artificial or naturally occurring (Jauron and Granstrom, 1989). In the artificial category, microbial/eukaryotic cells will be artificially entrapped inside of or attached to numerous matrices or supports where they are kept in or not kept in a viable state, this depend on the amount of harmfulness of the immobilisation procedure itself (Jauron and Granstrom, 1989).

Polysaccharide gel matrices, such as Ca-alginate hydrogels, are one of the most regularly used materials for harmless cell entrapment (Kandimalla, 2008). Cell attachment to an organic or inorganic substratum may be attained by forming covalent bonds between cells and the support using cross-linking agents (Junter and Jouenne, 2017). This immobilisation method is commonly incompatible with cell viability. The unstructured adsorption of the microbial cells to the different forms of carrier gives natural immobilised cell systems in which cells are attached to their support by non-covalent bonds, generally not specific interactions for example electrostatic interactions (Junter and Jouenne, 2017). In appropriate environmental conditions, this initial adsorption step may be followed by colonisation of the support, leading to the formation of a biofilm in which microorganisms are entrapped within a matrix of extracellular polymers secreted by themselves (Junter and Jouenne, 2017). Biofilms are securely attached to their substratum rather than purely adsorbed cells. therefore, they offer more practical as an immobilised cell system. Surface colonisation to procedure biofilms is a universal bacterial strategy for survival, and undesirable biofilms may occur on inert or living supports that may be in natural or in biological surroundings and also in industrial systems (Junter and Jouenne, 2017).

Aim of the Project

This research will build on the methods discussed in the paper written by Hobbs et al. (1989). The aim will be to use dispersed growth of Streptomyces in a liquid culture but will also aim to increase the antibiotic yield from this research by using immobilised cells. Coke (a form of coal) will be used to immobilise the cells, and will be used and looked at to determine whether the once the cells were immobilised will they grow to gain a higher yield of antibiotics. The cells will be immobilised but they will not be dead, they will not necessarily be able to replicate in this state which is the perfect state and condition for the antibiotic producing cells.

Objectives of the Project

  • Determine if antibiotic yield can be increased.
  • Optimise previous method.
  • Apply method of increasing antibiotic yield.
  • Determine whether immobilisation will increase the yield of antibiotic.

 

Method

Methods taken from paper written by Hobbs et al. (1989) this method will be built upon by using the principle of immobilising the cells with the use of coke to determine whether or not antibiotic yields will be improved and increase (Lebeau, 1996). Whilst using the method from the study by Hobbs et al. (1989) before growth conditions are set the carrier (coke) will be prepared and then the Streptomyces will be fixed to the carrier, then the method will continue to be carried out

(El-Enshasy et al., 1996).***

.

Work plan

Below is a table of a proposed schedule and work plan for the research. It is imperative that all the work is carried out carefully and that there is plenty of time for all the work to be carried out to the best standard.

Resources

Equipment and/or Resources

Costing (approximate number)

Laboratory equipment

£10,000

Consumables

£4,000

Computer hardware and software

£2,000

Travelling expenses

£1,000

Laboratory Technician x2

£15,000

Biologist x2

£30,000

Total

£62,000

Impact statement

The use of polyanions and immobilised cells will be used to reduce the problems associated with the growth in pellet form will be studied and the research will increase the biomass yield and also it will give an increased yield of actinorhodin which is an antibiotic that is blue pigmented and is a secondary metabolite. This research will look to increase the yield of the antibiotic (actinorhodin/OD unit).

Increasing the antibiotic yield using dispersed growth of Streptomyces in a liquid culture will mean that as well as the benefits of dispersed growth of Streptomyces in a liquid culture there will also be more antibiotics produces whereas in the initial method there was no increase in antibiotic yield. This will also open up the capability of immobilised cells and may be beneficial in the scientific field as a method that can be applied to similar microorganisms.

An increase in the understanding of Streptomyces, a microorganism group, will be a benefit of this study by using a method of growing it that allows to understand the physiology of the cell and to look at how immobilised cells optimise this and allow further understanding of how the antibiotic grows and why the yield would increase when cells were immobilised.

References

  1. AMR (2016). THE REVIEW ON ANTIMICROBIAL RESISTANCE. [online] HM Government. Available at: https://amr-review.org/sites/default/files/160518_Final%20paper_with%20cover.pdf.

(AMR, 2016)

  1. Blaskovich, M., Butler, M. and Cooper, M. (2017). Polishing the tarnished silver bullet: the quest for new antibiotics. Essays In Biochemistry, 61(1), pp.103-114.
    (Blaskovich et al., 2017)
  2. Chaumeil, M., Najac, C. and Ronen, S. (2015). Studies of Metabolism Using 13C MRS of Hyperpolarized Probes. Methods in Enzymology, pp.1-71.

(Chaumeil, 2015)

  1. Dervakos, G. and Webb, C. (1991). On the merits of viable-cell immobilisation. Biotechnology Advances, 9(4), pp.559-612.

(Dervakos and Webb, 1991)

  1. Doleyres, Y. and Lacroix, C. (2005). Technologies with free and immobilised cells for probiotic bifidobacteria production and protection. International Dairy Journal, 15(10), pp.973-988.

(Doleyres and Lacroix, 2005)

  1. El-Enshasy, H., Farid, M. and El-Diwany, A. (1996). Oxytetracycline production by free and immobilized cells of Streptomyces rimosus in batch and repeated batch cultures. Immobilized Cells – Basics and Applications, Proceedings of an International Symposium organized under auspices of The Working Party on Applied Biocatalysis of the European Federation of Biotechnology Noordwijkerhout, pp.437-443.
    (El-Enshasy et al., 1996)
  2. Feeney, M. (2015). How does one culture streptomyces?. [online] Quora. Available at: https://www.quora.com/How-does-one-culture-streptomyces [Accessed 3 Dec. 2018].

(Feeney, 2015)

  1. Guthrie, E., Flaxman, C., White, J., Hodgson, D., Bibb, M. and Chater, K. (1998). A response-regulator-like activator of antibiotic synthesis from Streptomyces coelicolor A3(2) with an amino-terminal domain that lacks a phosphorylation pocket. Microbiology, 144(3), pp.727-738.
    (Guthrie et al., 1998)
  2. Hobbs, G., Frazer, C., Gardner, D., Cullum, J. and Oliver, S. (1989). Dispersed growth of Streptomyces in liquid culture. Applied Microbiology and Biotechnology, 31(3).

(Hobbs et al., 1989)

  1. Hodgson, D. (2000). Primary metabolism and its control in streptomycetes: A most unusual group of bacteria. Advances in Microbial Physiology, pp.47-238.
    (Hodgson, 2000)
  2. Jaurin, B. and Granstrom, M. (1989). ?-Glucosidase genes of naturally occurring and cellulolytic Streptomyces species: characterization of two such genes in Streptomyces lividans. Applied Microbiology and Biotechnology, 30(5).
    (Jauron and Granstrom, 1989)
  3. Junter, G. and Jouenne, T. (2017). Immobilized Viable Cell Biocatalysts: A Paradoxical Development ☆. Reference Module in Life Sciences.

(Junter and Jouenne, 2017)

  1. Kandimalla, V., Tripathi, V. and Ju, H. (2008). Biosensors based on immobilization of biomolecules in sol-gel matrices. Electrochemical Sensors, Biosensors and their Biomedical Applications, pp.503-529.

(Kandimalla, 2008)

  1. Lebeau, T., Jouenne, T., Mignot, L. and Junter, G. (1996). Double-chambered bioreactors based on plane immobilized-cell membrane structures. Immobilized Cells – Basics and Applications, Proceedings of an International Symposium organized under auspices of The Working Party on Applied Biocatalysis of the European Federation of Biotechnology Noordwijkerhout, pp.532-537.
    (Lebeau, 1996)
  2. Leenen, E., Dos Santos, V., Tramper, J. and Wijffels, R. (1996). Characteristics and selection criteria of support materials for immobilization of nitrifying bacteria. Immobilized Cells – Basics and Applications, Proceedings of an International Symposium organized under auspices of The Working Party on Applied Biocatalysis of the European Federation of Biotechnology Noordwijkerhout, pp.205-212.
    (Leenen et al., 1996)
  3. Lindsey, K., Yeoman, M., Black, G. and Mavituna, F. (1983). A novel method for the immobilisation and culture of plant cells. FEBS Letters, 155(1), pp.143-149.

(Lindsey et al., 1983)

  1. Vecht-Lifshitz, S., Magdassi, S. and Braun, S. (1990). Pellet formation and cellular aggregation inStreptomyces tendae. Biotechnology and Bioengineering, 35(9), pp.890-896.
    (Vecht-Lifshitz et al., 1990)
  2. Wandrey, C. (1996). Why immobilize?. Immobilized Cells – Basics and Applications, Proceedings of an International Symposium organized under auspices of The Working Party on Applied Biocatalysis of the European Federation of Biotechnology Noordwijkerhout, pp.3-16.

(Wandrey, 1996)

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