Presentation on theme: "A Systems Approach to advanced enzyme technology"— Presentation transcript:
1A Systems Approach to advanced enzyme technology DINAZYMEA Systems Approach to advanced enzyme technology
2Background History of enzymes Alcoholic fermentation oldest known enzyme reactionY + G A + CO2Phenomena believed to be spontaneous reactions until 1857, when the French chemist Louis Pasteur proved that fermentation occurs only in the presence of living cells.Subsequently the German chemist Eduard Buchner discovered (1897) that a cell-free extract of yeast can cause alcoholic fermentation.The ancient puzzle was then solved; the yeast cell produces the enzyme and the enzyme brings about the fermentationAs early as 1783 the Italian biologist Lazzaro Spallanzani had observed that meat could be digested by gastric juices extracted from hawks.
3Background History of enzymes Probably first experiment in which a vital reaction was performed outside the living organismAfter Buchner's discovery scientists assumed that fermentations and vital reactions in general were caused by enzymesNevertheless, all attempts to isolate and identify their chemical nature were unsuccessfulIn 1926 the American biochemist James B. Sumner succeeded in isolating and crystallizing urease.
4Background History of enzymes Four years later pepsin and trypsin were isolated and crystallized by American biochemist John H. NorthropEnzymes were found to be proteins, and Northrop proved that the protein was actually the enzyme and not simply a carrier for another compoundResearch in enzyme chemistry in recent years has shed new light on some of the most basic functions of lifeRibonuclease, a simple three-dimensional enzyme discovered in 1938 by American bacteriologist René Dubos.Isolated in 1946 by American chemist Moses unitzSynthesized by American researchers in 1969
6Background History of enzymes The synthesis hooks 124 molecules in a specific sequence to form the macromoleculeLed to identification of those molecular areas that carry out its chemical functionsOpened up the possibility of creating specialized enzymes with new propertiesThis potential has been greatly expanded in recent years by genetic engineering techniques that have made it possible to produce some enzymes in great quantity
9Industry drawbacksNon-specific reactions may result in poor product yields.High temperatures and/or pressures needed to drive reactions lead to high energy costs. May require large volumes of cooling water downstream.Harsh and hazardous processes involving high temperatures, pressures, acidity or alkalinity need high capital investment, and specially designed equipment and control systems.Unwanted by-products may prove difficult or costly to dispose of.High chemical and energy consumption, and harmful by-products have a negative impact on the environment.
10Drawbacks eliminated by enzymes Reactions carried out under mild conditionsHighly specificInvolve very fast reaction ratesReactions are carried out by numerous enzymes with different roles.Industrial enzymes originate from biological systems which contribute to sustainable development through being isolated from microorganisms which are fermented using primarily renewable resources.Small amounts of enzymes are required to carry out chemical reactionsReaquires little storage space.uncomplicated and widely available equipment can be usedReactions are easily controlled and can be stopped when the desired degree of substrate conversion has been achieved.Reduce the impact of collateral damage on the environment by reducing the consumption of chemicals and energy, and the subsequent generation of waste.Developments in genetic and protein engineering have led to improvements in the stability, economy, specificity and overall application potential of industrial enzymes.
11What are enzymes?An enzyme is a protein which acts as a specific biological catalyst facilitating a given reaction by lowering the amount of required energy.To date, scientists have identified over 1,500 different enzymes.
12What are enzymes? Six main classes by type of reaction catalyzed Classes are split into groups and subclassesEx., lactase catalyzes the conversion of milk / sugar to galactose and glucoseLactase has the systematic name beta-D-galactoside galactohydrolase, and the classification number EC
13SIX MAIN ENZYME CLASSES REACTION PROFILE1: OxidoreductasesInvolves movement of electrons from one molecule to another. In biological systems we usually see the removal of hydrogen from the substrate. Enzymes in this class are called dehydrogenases. Ex., alcohol dehydrogen-ase catalyzes reactions of the type R-CH2OH + A → R-CHO + H2A, where A is an acceptor molecule. If A is oxygen, the relevant enzymes are called oxidases; if A is hydrogen peroxide, the relevant enzymes are called peroxidases.2: TransferasesThis class of enzymes catalyzes the transfer of groups of atoms (radicals) from one molecu-le to another. Aminotransferases or transaminases promote the transfer of an amino group from one amino acid to an alpha-keto-acid.3: HydrolasesHydrolases catalyze reactions between a substrate and water, and bind water to certain molecules. In this way larger molecules are broken up into smaller units. This class of enzymes catalyzes the cleavage of peptide bonds in proteins, glucosidic bonds in carbohydrates, and ester bonds in lipids.4: LyasesLyases catalyze the addition of groups to double bonds or the formation of double bonds through the removal of groups. Thus bonds are cleaved using a different principle to hydrolysis. Pectate lyases, for example, split the glycosidic linkages by beta-elimination.5: IsomerasesIsomerases catalyze the transfer of groups from one position to another on the same molecule. These enzymes change the structure of a substrate by rearranging its atoms.6: LigasesLigases join molecules together with covalent bonds. These enzymes participate in biosynthetic reactions where new groups of bonds are formed. Such reactions require the input of energy in the form of co-factors such as ATP.
14Globular, water soluble proteins, (few exceptions) What are enzymes?Globular, water soluble proteins, (few exceptions)Allows / facilitates chemical reactions to occur such as those that release nutrients from feed during digestionWithout the enzyme catalyst the reaction would either not take place or would happen very slowlyIf a reaction is favorable ( ∆G < 0), the activation energy E(act) determines how fast it will go.
15What are enzymes?Though an enzymatic catalyst takes part in the chemical reaction it remains unchanged and is available to repeat the task
16Virtually all enzymes employed in the feed industry are hydrolases. What are the most important enzymes to our industry?Virtually all enzymes employed in the feed industry are hydrolases.Some enzymes that are of practical value to the livestock industry:Xylanases, amylases, phytases, proteases, cellulases, betaglucanases, and pentosanases, are available for use in diet formulations.These enzymes can be mixed and matched to form an enzyme cocktail to fit any particular diet need.
17Why are enzymes needed in feed formulations? Trials confirm that enzyme supplementation results in improved animal performance.Young animals lack many endogenous enzymes or sufficient quantities thereoff.Sick animals may have a damaged intestinal lumen resulting in limited nutrient absorption.Animals under stress or at a high level of production may have an impaired digestive system.
18Why are enzymes needed in feed formulations? Problems in feed ingredients:Raw materials may contain anti-nutritive factors. Ex. pentosans or betaglucans present in wheat or barley.Addition of appropriate enzyme aids digestion of the material improving feed value.Increasing environmental awareness and restrictions on pollutants and contaminants confirm the value of enzymes in the breakdown of such materials. Ex Phytase/ phosphorus
19How do enzymes work?SpecificitySpecific enzymes may be incorporated into specific diets in order to solve specific problems
20How do enzymes work?Enzyme catalyzed reactions are often from 100 million to more than 10 billion times faster than the same reaction in the absence of the enzyme.Most enzymes catalyze the transfer of electrons, atoms or functional groups.
21Factors influencing enzyme activity Optimum pHOptimum Temperature
26Factors influencing enzyme activity Optimum pH: pH at which enzymes operate best. Activity decreases on either side of pH optimum.
27Factors influencing enzyme activity Optimum Temperature:Within a given range, for every 10 degrees the temperature increases, enzyme activity doubles.Enzymes become denatured at elevated temperatures.Enzymes have an optimum temperature which varies according to:Enzyme source.Salt levels in the medium to which the enzyme is added. (For example, amylases from animal sources are less heat stable than those from fungal sources (Aspergillus) which are in turn less stable than bacterial amylases (Bacillus).Mineral Content: Certain minerals stabilize enzymes while others cause inactivation. Calcium and magnesium are essential for good starch breakdown (amylases) and increase enzyme stability to temperature. Heavy metals such as iron are typically detrimental to enzymes, and may in some cases be used to inactivate or stop enzyme reactions.
28Enzyme concentrationNormally enzymes are present in cells in low concentrations.As enzyme concentration increases the rate of the reaction increases linearly, because there are more enzyme molecules available to catalyse the reaction.At very high enzyme concentration the substrate concentration may become rate-limiting, so the rate stops increasing.
29Substrate concentration As the substrate concentration increases, the rate increases because more substrate molecules can collide with enzyme molecules, so more reactions will take place.As substrate concentration gets higher the enzyme molecules become saturated so there are few free enzyme molecules. Adding more substrate doesn't make much difference (though it will increase the rate of E-S collisions).The maximum rate at infinite substrate concentration is called vmax,The substrate concentration that gives a rate of half the maximum rate vmax is called KM.The vmax and KM values are useful for characterising an enzyme.A good enzyme has a high vmax and a low KM.
31Covalent modification Activity of some enzymes is controlled by others.These enzymes modify the protein chain by cutting it, or adding a phosphate or methyl group.Turns inactive enzyme into active (or vice versa).Used to control many metabolic enzymes and to switch on enzymes in the gut e.g. hydrochloric acid in stomach activates pepsin activates rennin.
32InhibitorsInhibitors inhibit the activity of enzymes, reducing the rate of their reactions.Found naturally, but are also used artificially as drugs, pesticides and research tools.
33Inhibitors There are two kinds of enzymatic inhibitors. Non-competitiveCompetitive
34Competitive Inhibitors Molecule has similar structure to normal substrate molecule. Fits into active site of the enzyme.Competes with substrate for the active site, so reaction is slower.Increase KM for enzyme, but no effect on vmax.The rate can approach a normality if substrate concentration is increased sufficiently.The sulphonamide anti-bacterial drugs are examples of competitive inhibitors.
35Non-competitive inhibitors Inhibitor molecule is different in structure than the substrate moleculeWill not fit into active site.Binds to another part of the enzyme molecule.Change enzyme and active site shape so it no longer binds substrate molecules. Result is reduction of active enzyme numbers (just like decreasing the enzyme concentration). Therefore decrease vmax, but have no effect on KM.Reversible inhibitors - bind weakly and can be washed out.Irreversible inhibitors - bind tightly and cannot be washed out.Poisons like cyanide, heavy metal ions and some insecticides are all examples of non-competitive inhibitors.
36RATE EQUATION FOR PRODUCT INHIBITION Michaelis-Menten equation
37Allosteric EffectorsActivity of some enzymes is controlled by certain molecules binding to a specific regulatory or allosteric site on the enzyme.Allosteric site is distinct from the active siteDifferent molecules can inhibit or activate the enzyme, allowing sophisticated control of the reaction rateFew enzymes can do this. They are often at the start of long biochemical pathwaysGenerally activated by the substrate of the pathway and inhibited by the product of the pathway, thus only turning the pathway on when it is needed
39Economic benefits Increases daily weight gain Increases egg production Lowers feed conversionMore uniform weights / increased nutrient absorptionLower incidence of digestive problems caused by unassimilated fiber which also improves litter qualityReduces fecal volume and nitrogen excretion levelsCleaner eggs and better egg yolk colorUse of lower cost ingredientsMaintains and improves performance levelsIncreases ratio of lean to fat tissueCan "inactivate" mycotoxins in feeds
40What is Dinazyme? Dinazyme B/W Dry and Liquid Several types of enzyme technologies are offered as DinazymeDinazyme B/W Dry and LiquidDinazyme C/S PBM Dry and LiquidDinazyme PSE, (Phytase) Dry
41What is Dinazyme C/S PMB Supplement for corn soy based poultry and pig diets containing high glucan barley levels.
42What is Dinazyme C/S PMB A diet supplement which enhances nitrogen utilization and increases protein digestibility with the active ingredient protease, resulting in increased absorption of amino acids and peptides.DINAZYME C/S® also contains amylase-breaks down starch content and Xylanase, a complex hydrolytic enzyme preparation which has an effect on hemicellulose substrates containing xylan, manan and glucan.A combination of amylase, Xylanase and protease boosts the digestibility of typical corn and soybean meal-based diets, resulting in more nutrients available for growth.Inclusion of DINAZYME C/S® in diet supplements provides endogenous enzymes animals lack or produce in low amounts.
43WHAT MAKES DINAZYME MORE EFFECTIVE THAN OTHER ENZYMECOMBINATIONS Effective action due to presence of other important hydrolytic enzymes, which decompose cellulose, lichenin, araban and pectin.Dinatec makes use of important technical concepts such as:Covalence modification,The use of specific allosteric substances and enzyme co-factors that are conducive to higher enzymatic efficacyEnzyme concentration
44What can Dinazyme C/S PMB do for you? Contents / effects:Protease, enhanced nitrogen utilization and increased protein digestibilityAmylase, increased digestibility of starch in pig and poultry dietsBetaglucanase, reduced digesta viscosity in poultry diets; decreases anti- nutritional effects of NSP*; reduces soluble NSP in disgesta.Pectinase, more complete hydrolysis (digestion) of pectins in wheat and corn based dietsXylanase reduces digesta viscosity; decreases anti-nutritional effects of NSP; reduces soluble NSP in digesta hence increased absorption of amino acids and peptides.* Non Starch Polysaccharide
45Why should you use Dinazyme? High energy diets high on starch and protein content are desirable at an early age for the monogastric.Young animal's endogenous enzyme system not fully developed. Unable to adapt quickly enough for demands of current feed management programs.Immature pancreas needs time to adapt to new diet and produce necessary amounts and types of digestive enzymes.Result - Undigested feed is wasted.Undigested feed promotes "nutritional scours" and provides substrate for the growth of diarrhea-causing pathogens.
46Why should you use Dinazyme? The Solution… Dinazyme C/S-PMBTo supplement the immature endogenous enzyme system.To maximize performance, even with limited digestive capacity, e.g. case of young animals or rapid diet changes.To optimize nutrient utilization of high energy feedstuffs.To enable use of normally undigestible alternate lower cost ingredients
47ECONOMICSData suggest that an average improvement in nutrient utilization of 3 – 5% can be obtainedLeeson and Summers (1976) reported that high moisture content corn harvest necessitated high temperature drying & time retention conditions, reduced ME value of corn by as much as 3% compared to the expected value.
48Specifications for Dinazyme C/S PBM EFFICACYEffective over a wide pH and temperature range.PACKAGINGAvailable in 5, 10 and 20 kg pails or 55 lb. bags.STORAGEIn dry location. Do not exceed 26°C.SHELF LIFEOne year in original sealed container. Three months in stored premixes and feedstuffs.USE & DOSEFor any corn/soy based feed. Layer/Breeder feeds. 200 grms/metric ton, Broiler feeds. 250 grms/metric ton. Pig diets. 300 grms/metric ton.