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Advantages and disadvantages enzymes used in the food industry
Lipase practicals
Lipase investigation
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4.2 CASE STUDY: LIPASES
4.2.1 Background
Lipases are a type of hydrolases which catalyze the conversion of fats/oils to free fatty acids and glycerol. Lipases are placed after proteases and carbohydrases in the world enzyme market and have about 5% of enzyme market. They are one of the most important group of biocatalysts for biological applications and are quite important enzymes from both physiological and biotechnological view point. The rising interest in lipases is mainly because of wide industrial applications of this enzyme, including detergent formulation, pharmaceuticals synthesis, oils/fats degradation, and cosmetics production.
Lipases currently attract a large amount of attention mainly because of their unique characteristics: substrate specificity, regio-specificity and chiral selectivity (Castro-Ochoa et al., 2005). Like carbohydrases and proteases, lipases that are of microbial origin they enjoy larger industrial importance because they are more stable (as compared to plant and animal origin lipases) and they can be obtained in bulk at comparatively low cost. Because of the characteristics, novel biotechnological applications have been established using lipases for the synthesis of biopolymers and the production of biodiesel, enantiopure, biosensors and flavour compounds (Bornscheuer et al., 2002).
4.2.2 Sources
Lipases are are produced by various plants, animals and microbes. Animal origin Lipases include Human Pancreatic Lipase, Horse Pancreatic Lipase, Pig Pancreatic Lipase and Guinea Pig Pancreatic Lipase. The plant sources rich in Lipases are Avocado, Walnut, Coconut, Lentils, Chickpea, Papaya, Mung Bean, Oats and Eggplant Lipases of microbial origin, mainly bacterial and fungal, represent the most used cl...
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...of publications on the same have grown from 1990, with maximum publications being from Brazil.
CSTR is the most preferred choice of Bioreactor for industrial-scale production of enzymes. It is an easily constructed, versatile, cost-effective reactor, it’s well -mixed nature permits straightforward control over the temperature and pH of the reaction and the supply or removal of gases and it can be readily adapted for automatic control in general that allowing fast response to changes in operating conditions. Also, CSTR is relatively easy to maintain and operate.
The major impediments to the exploration of commercial enzymes are their yield, stability, specificity and cost of production. Newer enzymes for use in commercial applications with desirable biochemical and physicochemical characteristics and low production costs have been focus of much research today.
Moreover, the class average curve shows a similar trend, as the curve flattens, at 70% but with an enzyme activity of 5.3 x10-3 seconds. This indicates that even though the saturation point is the same it was considerably lower than our results, which could indicate sources of systematic error in the design of the practical.
Enzymes are proteins that increase the rate of chemical reaction by lowering their activation energy. The enzyme glucose oxidase is one of the most widely used enzyme as an analytical reagent due to its ability to identify the presence of glucose, its low cost and good stability. This report discusses the role of enzymes concentration in biological reactions and the catalytic activity of glucose oxidase on D-Glucose. The activity was studied by spectrophotometry and the results were first tabulated and then plotted. The results of this experiment indicate that the enzyme concentration has no major affect on the rate of
The Effect of Temperature on an Enzyme's Ability to Break Down Fat Aim: To investigate the effect of temperature on an enzyme’s (lipase) ability to break down fat. Hypothesis: The graph below shows the rate increasing as the enzymes get closer to their optimum temperature (around 35 degrees Celsius) from room temperature. The enzyme particles are moving quicker because the temperature increases so more collisions and reactions occur between the enzymes and the substrate molecules. After this the graph shows the rate decreasing as the enzymes are past their optimum temperature (higher than). They are getting exposed to temperatures that are too hot and so the proteins are being destroyed.
An Investigation into the Effect of Lipase Concentration on the Hydrolysis Of Fats Using the data loggers a recording of the pH was taken every 5 seconds and for each experiment the data loggers produced graphs of the change in pH. From each of these graphs a gradient was calculated which showed the rate of pH change per second. Firstly I calculated the gradients by choosing the steepest section of the graph and dividing the change in pH of this section by the time. However this method proved to be quite inaccurate giving very varied results, for example in these results the average rate of reaction for the 4% lipase solution (-0.457 pH/min) was lower than the 3% lipase solution (-0.471 pH/min). Also the rates in the 2% lipase solution ranged from -0.01 pH/min to -0.95 pH/min showing little reliability in the results. This was partly as I was only guessing which the steepest part of the graph was.
than double the number in 2005, and nearly quadruple the number in 2000 (Salam, 2017). Drug
Many factors, for example, pH and temperature affects the way enzymes work by either increasing the rate or determining the type of product produced (). The report, therefore, analyses the effects of the enzyme peroxidase in metabolic reactions and determining its optimum temperature in the reactions.
Despite of general properties of enzymes, the properties also varies from where it comes from and how it been produced. For instance, the enzymatic saccharification method in lignocellulosic bioethanol is generated by hydrolyzing cellulose and hemicelluloses. This method gets high attention because of its higher theoretical yield compared to other methods (Taneda et al., 2012). Acremonium cellulolyticus with high activities of cellulase, amylase and pectinase enzymes allow it for the easy separation of solids/liquids in potato pulp, resulting in high saccharification efficiency and a high recovery rate of products (Gao et al., 2014). On the other hand, Enzyme-modified carboxymethyl starch (ECMS) is beneficial in enhancing water holding capacity, emulsion stability and improving sensory characteristics of sausages with a declined fat content (Luo and Xu, 2011). Lipases and phospholipases of dormant cotton seeds have stability in heat, various media and nature of the hydrolysis of the lipids properties (Rakhi...
Valdes, Constanza. "Brazil Emerges as Major Force in Global Meat Markets." AmberWaves April (2006). Web. 30 Oct. 2011.
In the current economic times the development and growth of any economy has come to a near stop or at least to a drastic slow down. The face of the global economic environment has changed and many new countries are starting to change the way their country and the rest of the world does business. One such nation is Brazil, who has turned around their own economic troubles and is becoming one of the fastest growing economies in the world (World Factbook). Brazil has started developing its economy and using the opportunity to achieve a level of respect in the world.
In this lab, it was determined how the rate of an enzyme-catalyzed reaction is affected by physical factors such as enzyme concentration, temperature, and substrate concentration affect. The question of what factors influence enzyme activity can be answered by the results of peroxidase activity and its relation to temperature and whether or not hydroxylamine causes a reaction change with enzyme activity. An enzyme is a protein produced by a living organism that serves as a biological catalyst. A catalyst is a substance that speeds up the rate of a chemical reaction and does so by lowering the activation energy of a reaction. With that energy reactants are brought together so that products can be formed.
My prediction was very accurate as there were little products at room temperature, and according to my results the optimum temperature was only about 1ºC higher than my prediction. I also correctly predicted that the enzymes would denature after 40oC and that the graph would be exponential. Conclusion The graph starts with little carbon dioxide production at the low temperatures.
plasma membranes, meaning animals and plants contain lipids. In this paper I will display and
Purpose: The purpose of this lab is to explore the different factors which effect enzyme activity and the rates of reaction, such as particle size and temperature.
There are many more lipids than I have mentioned in my research paper, there are over a 100 know lipids. Lipids are very important for our body and cells and they carry out many function. They provide nutrients for our body. Lipids are a category of nutrients. Lipids consist of fats, oils, and waxes and are very important for are body’s health. Lipids are important for the human body because they are for storing energy, they’re good at storing energy because they can concentrate a group of calories in a smaller area. Lipids are also used to make soaps, detergents and waxes. These are things that we use in every day life.
5 test tubes were prepared for dilution respectively to 5 spec tubes that had the inhibitor and water and ready for the enzyme addition. Recordings were done every 60 seconds for 3 minutes. Reaction rate was then calculated after time ended. After having used the inhibitor, the steps were repeated but replace the inhibitor with water as control and experimented for the rates without the inhibitor. Percentages were graphed by the percentage inhibition versus the substrate concentration for the inhibitor. Part 5 of the experiment was to determine the effect of temperature or pH on the reaction rate. In doing so, each group in the lab was designated a particular enzyme that was exposed in different temperatures (Schultz, 2006). The enzymes were exposed before the beginning of the experiment into these different temperatures: boiling, warm (heat), room temperature, cold (ice bath), and frozen. Each enzyme was allowed back to room temperature before adding the buffered catechol with the 1 ml of enzyme into the spec tube (Schultz, 2006). Reaction rate was then determined from the reading. Absorbance versus time was plotted with the determined initial rate of each