The culture condition for maximum lipase production by isolated micrococcus

 

Table Of Contents


Chapter ONE

INTRODUCTION

  • 1.1Introduction
  • 1.2Background of Study
  • 1.3Problem Statement
  • 1.4Objective of Study
  • 1.5Limitation of Study
  • 1.6Scope of Study
  • 1.7Significance of Study
  • 1.8Structure of the Research
  • 1.9Definition of Terms

Chapter TWO

LITERATURE REVIEW

  • 2.1Overview of Lipase Enzyme
  • 2.2Importance of Lipase in Biotechnology
  • 2.3Sources of Lipase
  • 2.4Factors Affecting Lipase Production
  • 2.5Microbial Lipase Production
  • 2.6Optimization of Lipase Production
  • 2.7Purification of Lipase Enzyme
  • 2.8Characterization of Lipase Enzyme
  • 2.9Applications of Lipase in Industries
  • 2.10Recent Advances in Lipase Research

Chapter THREE

SYSTEM DESIGN AND IMPLEMENTATION

  • 3.1Research Methodology Overview
  • 3.2Selection of Microorganism
  • 3.3Isolation and Identification of Micrococcus
  • 3.4Lipase Production Conditions
  • 3.5Experimental Design for Lipase Production
  • 3.6Enzyme Assay Methods
  • 3.7Purification Techniques
  • 3.8Characterization Techniques

Chapter FOUR

SYSTEM TESTING AND EVALUATION

  • 4.1Lipase Production Results
  • 4.2Effect of Different Parameters on Lipase Production
  • 4.3Optimization Results
  • 4.4Purification Yield and Techniques
  • 4.5Characterization Data Analysis
  • 4.6Comparison with Literature Findings
  • 4.7Discussion on Enzyme Stability
  • 4.8Implications of Findings in Biotechnology

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • 5.1Summary of Findings
  • 5.2Conclusion
  • 5.3Recommendations for Future Research
  • 5.4Practical Applications of Research
  • 5.5Contribution to Lipase Enzyme Field

Project Abstract

Lipases are enzymes that catalyze the hydrolysis of long-chain triglycerides into glycerol and fatty acids and have significant industrial applications in various fields. Micrococcus species are known to produce lipase enzymes, and optimizing culture conditions for maximum lipase production is essential for industrial enzyme production. This study aimed to determine the culture conditions for maximum lipase production by an isolated strain of Micrococcus. The isolated Micrococcus strain was cultured in different media compositions and growth conditions, including variations in pH, temperature, agitation, and incubation time. The lipase activity was assayed using a spectrophotometric method, and the results were analyzed to determine the optimal culture conditions for lipase production. The findings revealed that the isolated Micrococcus strain exhibited maximum lipase production when cultured in a medium containing olive oil as the carbon source and peptone as the nitrogen source. The optimum pH for lipase production was found to be 7.0, with a temperature of 37Β°C, agitation at 150 rpm, and an incubation period of 48 hours. Under these conditions, the isolated Micrococcus strain showed a significant increase in lipase production compared to other culture conditions tested. The study provides valuable insights into the culture conditions required for maximizing lipase production by an isolated strain of Micrococcus, which can be beneficial for industrial enzyme production processes. Further research can focus on scaling up the production process and optimizing other parameters to enhance lipase yield for commercial applications.

Project Overview

<p> </p><p>1.0 &nbsp; INTRODUCTION</p><p>Ugba also called ukpaka is a popular food delicacy in Nigeria especially among Ibo ethnic group. It is rich in protein and is obtained by a solid state fermentation of the seed of African oil bean tree (Pentaclethra macrophyllaBenth). It is essential food item from various traditional ceremonies where it is mixed with slices of boiled stock fish (ugba and okpoloko). The natural fermentation of the seed which at present is still done at the house-hold level, renders the production nutritious, palatable and non-toxic (Enujiugha, 2002).</p><p>Its production, like many African fermented foods depends, entirely on mixed fermentation by microorganism from diverse source.</p><p>Some of these seeds have been exploited as soup bases such as Gbegiri from Vigna unguicuata (Akanbi, 1992). Others are fermented and used as condiments and seasonings such as okpei from Prosopis africana (Achi, 1992) and ogiri from Ricinus cummunis (Odunka, 1989). Another of such seeds is the African oil bean seed (Pentaclethra macrophylla Benth), a highly nutritious leguminous crop seed abundant in the rain forest areas of west and central Africa.</p><p>Pentaclethra macrophylla Benth is a large woody plant abundant in the rain forest areas of west and central Africa. It’s origin in Nigeria is believed to be around 1937 (Ladipo, 1984); where it is found in the South Nigeria, (Mbajunwa et al, 1998).</p><p>“Ugba” Pentaclethra macrophylla Benth belongs to the Family Leguminosae and sub-family microsoideae (Keay, 1989 and NFTA, 1995).</p><p>Ugba seeds are irregular and oval, they are flat, black and hard pods. It is composed of oil, protein and small amounts of carbohydrate (Obeta, 1982).</p><p>Production of Ugba is still on age old traditional family in the rural area. The fermentation depends on random inoculation of boiled slices of the oil bean seed by microorganism within he immediate environment. Earlier report attribute the sources of the micro-organism to the leaves used in packaging, human handling, container and utensils used in processing (Obeta, 1993, Odunfa &amp; Oyeyiola, 1985).</p><p>A number of researches have been carried out to know what causes this fermentation, and was attributed to micro-organisms that are probably introduced through the air, water, and banana leaves. Organisms such asMicrococus roseus, Micrococcus luteus, Leuconostoc mesenteroides,Staphylococcus aureus, Staphylococcus epidermidis, Bacillus substilis,Bacillus megaterium and Bacillus circclans, E-Coli</p><p>Fermented African oil bean seed (ugba), has a high rate of susceptibility to microbial spoilage and therefore has a very short self life of 1-2 weeks (Enujiugha &amp; Olajundoye, 2001).</p><p>Manifestation of food spoilage are many and vary typically resulting in an off smell, colour, taste and texture.</p><p>Reports by Mbajunwa (1998) Obeta, (1983) and Nwagu et al. (2010) indicates that micrococcus species do not play an active role during microbial fermentation of Ugba.</p><p>However, further work on spoilage association of ugba by Nwagu et al(2010) showed that the population of Micrococcus sp increased with increase in keeping time of ugba. This indicates the ability of micrococcus to thrive in the alkalophilic environment while constituting as a spoilage organism of ugba. This may be attributed to the ability of microorganism to produce lipase, lipase, or protease able to utilize protein, carbohydrate or lipid content of ugba as source of nutrition (Njoku et al., 1990).</p><p>Lipase are defined as glycerol ester hydrolases (EC3.1.1.3) hydrolyzing tri-di and mono-glycerides present at oil-water interface (Saxena et al, 1999). Some lipases are also able to catalyze esterification, trans-esterification and enantioselective &nbsp;hydrolysis reaction (Nine et al, 2001, Shintre et al, 2002). The interest in microbial lipase production has increased in the last decades, because of its large potential in a wide range of industrial applications and additives in food processing (flavour modification).</p><p>1.1 &nbsp; Aims and Objectives</p><p>This work is aimed at the following;</p><p>a. &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; isolating micrococcus from fermented ugba</p><p>b. &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; producing lipase from the micrococcus from ugba</p> <br><p></p>

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