Effect of variation in temperature & pH levels on the activity of salivary am...Nidhi Sharma
This document describes an experiment to study the effects of temperature and pH levels on the activity of salivary amylase on starch. For the temperature experiment, starch solution was placed in test tubes at 5°C, 37°C and 50°C with saliva added. The test tube at 37°C reached the point where iodine no longer detected starch the quickest, showing optimal enzyme activity at body temperature. For the pH experiment, starch solution was adjusted to pH 5, 6.8 and 8 with saliva added. Activity was only observed at pH 6.8, as the enzyme does not function in acidic or alkaline environments.
pH is a measure of the concentration of hydrogen ions in a solution, with values below 7 indicating acidity and above 7 indicating alkalinity. There are several methods to measure pH, including using indicators that change color depending on pH and compare to a standard, using a hydrogen electrode immersed in the solution, or using a glass electrode and reference electrode to measure the voltage between them. pH sensors are important for quality control in industries like pharmaceutical, chemical, food production, and more.
Estimation of dna by diphenylamine methodjeevithaseyan
This document describes a method to estimate the concentration of DNA using diphenylamine. DNA reacts with diphenylamine under acidic conditions to form a blue-green complex. Various concentrations of a DNA standard are reacted with diphenylamine reagent and measured at 595nm to generate a standard curve. An unknown DNA sample is then reacted, measured and its concentration determined using the standard curve. Reagents, equipment, procedure and calculations are outlined to perform the diphenylamine method of DNA concentration estimation.
What is Gravimetric analysis, stepes invloved in gravimetry, Filteration medium in gravimetry, gravimetric factor, application, organic and inorganic prepecating agents
pH is defined as the negative logarithm of the activity of hydronium ions in a solution. The activity takes into account both the concentration and rational activity coefficient of hydronium ions. Sorensen established the pH scale, which runs from 0 to 14, with pH 7 being neutral. Below 7 solutions are acidic and above 7 they are basic. The scale provides a standardized way to express the hydrogen ion concentration or acidity level of solutions. Common applications of measuring and controlling pH include enhancing solubility, stability, purity, and biological activity of substances, as well as storage of products.
Osmosis is the spontaneous movement of water molecules through a semi-permeable membrane from a region of lower solute concentration to higher solute concentration in order to equalize the concentrations. It provides the means for water transport into and out of cells. The direction of osmosis depends on the solute concentrations on both sides of the membrane - if one side has a higher concentration than the other, water will diffuse into the lower concentration side. This movement of water allows cells to remain turgid and control their volume under different osmotic conditions by taking in or releasing water through osmosis.
This presentation gives us idea about Gravimetric Analysis which is widely used in chemistry. Hope This Helps !
For More Information - 19103083@student.hindustanuniv.ac.in
An enzyme is a substance that acts as a catalyst in living organisms, regulating the rate at which chemical reactions proceed without itself being altered in the process. The biological processes that occur within all living organisms are chemical reactions, and most are regulated by enzymes
Effect of variation in temperature & pH levels on the activity of salivary am...Nidhi Sharma
This document describes an experiment to study the effects of temperature and pH levels on the activity of salivary amylase on starch. For the temperature experiment, starch solution was placed in test tubes at 5°C, 37°C and 50°C with saliva added. The test tube at 37°C reached the point where iodine no longer detected starch the quickest, showing optimal enzyme activity at body temperature. For the pH experiment, starch solution was adjusted to pH 5, 6.8 and 8 with saliva added. Activity was only observed at pH 6.8, as the enzyme does not function in acidic or alkaline environments.
pH is a measure of the concentration of hydrogen ions in a solution, with values below 7 indicating acidity and above 7 indicating alkalinity. There are several methods to measure pH, including using indicators that change color depending on pH and compare to a standard, using a hydrogen electrode immersed in the solution, or using a glass electrode and reference electrode to measure the voltage between them. pH sensors are important for quality control in industries like pharmaceutical, chemical, food production, and more.
Estimation of dna by diphenylamine methodjeevithaseyan
This document describes a method to estimate the concentration of DNA using diphenylamine. DNA reacts with diphenylamine under acidic conditions to form a blue-green complex. Various concentrations of a DNA standard are reacted with diphenylamine reagent and measured at 595nm to generate a standard curve. An unknown DNA sample is then reacted, measured and its concentration determined using the standard curve. Reagents, equipment, procedure and calculations are outlined to perform the diphenylamine method of DNA concentration estimation.
What is Gravimetric analysis, stepes invloved in gravimetry, Filteration medium in gravimetry, gravimetric factor, application, organic and inorganic prepecating agents
pH is defined as the negative logarithm of the activity of hydronium ions in a solution. The activity takes into account both the concentration and rational activity coefficient of hydronium ions. Sorensen established the pH scale, which runs from 0 to 14, with pH 7 being neutral. Below 7 solutions are acidic and above 7 they are basic. The scale provides a standardized way to express the hydrogen ion concentration or acidity level of solutions. Common applications of measuring and controlling pH include enhancing solubility, stability, purity, and biological activity of substances, as well as storage of products.
Osmosis is the spontaneous movement of water molecules through a semi-permeable membrane from a region of lower solute concentration to higher solute concentration in order to equalize the concentrations. It provides the means for water transport into and out of cells. The direction of osmosis depends on the solute concentrations on both sides of the membrane - if one side has a higher concentration than the other, water will diffuse into the lower concentration side. This movement of water allows cells to remain turgid and control their volume under different osmotic conditions by taking in or releasing water through osmosis.
This presentation gives us idea about Gravimetric Analysis which is widely used in chemistry. Hope This Helps !
For More Information - 19103083@student.hindustanuniv.ac.in
An enzyme is a substance that acts as a catalyst in living organisms, regulating the rate at which chemical reactions proceed without itself being altered in the process. The biological processes that occur within all living organisms are chemical reactions, and most are regulated by enzymes
This document summarizes a protocol for estimating nitrate levels in drinking water. Nitrate testing is important to determine concentrations and ensure they remain below acceptable levels of 10mg/L, as excess nitrate can cause eutrophication and be dangerous to human health, potentially leading to methemoglobinemia or various cancers. The protocol uses sodium chloride, sulfuric acid, brusin sulphanilic acid, and potassium nitrate reagents to oxidize samples in a series of test tubes, which are then read spectrophotometrically to determine nitrate concentrations.
This document discusses the principles and proper use of balances. It explains that a balance measures the force of gravity on an object, or its weight. Weight is dependent on location, while mass remains constant. Electronic balances use electromagnetic forces rather than beams to counterbalance a sample and convert the electrical signal to a weight measurement. The document provides guidelines for operating balances accurately, including leveling, taring, and avoiding sources of error like vibration. It stresses the importance of calibration and quality control programs to ensure balance measurements are valid.
This document describes an experiment to determine the presence or absence of various secondary metabolites in a plant sample. Nine tests were performed to detect phytochemicals like saponins, glycosides, flavonoids, terpenoids, steroids, carotenoids, alkaloids, anthraquinones, and coumarins. Saponins and coumarins were found to be present, while the other phytochemicals were absent based on the observations from the chemical tests. The experiment was aimed at identifying phytochemicals in a given plant and determining which were present.
This document discusses acid-base balance and pH. It defines pH as the negative log of the hydrogen ion concentration. The pH scale ranges from 0 to 14, with values below 7 being acidic and above 7 being basic. The body maintains acid-base balance through buffer systems like bicarbonate and proteins, and respiratory and renal compensation mechanisms. Disturbances in acid-base balance can cause metabolic acidosis, metabolic alkalosis, respiratory acidosis, or respiratory alkalosis.
The document discusses carbohydrate structure and properties. It covers the biological and medical importance of carbohydrates, including their functions as energy stores and structural components. It also describes the chemical nature of carbohydrates as polyhydroxy alcohols with an aldehyde or keto group. Carbohydrate structure is examined using Fisher, Haworth and chair conformations. Carbohydrates are classified as monosaccharides, oligosaccharides like disaccharides, and polysaccharides including homo- and heteropolysaccharides. Important monosaccharides, derivatives, disaccharides and polysaccharides are identified. Properties of monosaccharides such as isomerism, optical activity, epimerism, hemiacetal/ketal formation,
1. Several qualitative tests can identify the presence of carbohydrates, including the Molisch test, iodine test, Benedict's test, Barfoed's test, Seliwanoff's test, and osazone tests.
2. The Molisch test uses alpha-naphthol and sulfuric acid to detect the presence of any carbohydrate, producing a purple ring at the interface. Benedict's test uses copper sulfate and citrate in an alkaline solution to detect reducing sugars based on the color of precipitation.
3. The iodine test detects polysaccharides like starch, producing colors from blue to reddish-brown depending on the type. Barfoed's test distinguishes monos
The document discusses enzymes, substrates, and how they interact. It defines enzymes as proteins that catalyze chemical reactions and substrates as molecules that enzymes act upon. It describes how enzymes and substrates form an enzyme-substrate complex, in which the substrate binds to the active site of the enzyme. This allows the enzyme to catalyze the reaction and convert the substrate into products, before releasing the products and binding with new substrates. The document explores models of enzyme-substrate binding, such as the lock-and-key and induced fit models. It also outlines the four steps of enzyme action and how factors like temperature can regulate enzyme activity.
Sampling in analytical chemistry sajjad ullahSajjad Ullah
Sampling is the process of obtaining representative samples of materials like solids, liquids, and gases. It is a critical step in analysis. For heterogeneous solids, several individual samples are taken and combined into a gross sample. For liquids, grab samples or devices like thieves or impingers are used. Gases can be sampled directly or with enrichment using adsorption tubes, impingers, or chemical reactions. The key steps are sampling, transport, analysis, and assessment. Careful sampling ensures accurate results.
This presentation discusses normality, which is a measure of concentration defined as the number of gram equivalents of solute per liter of solution. A normal solution contains 1 gram equivalent of solute per liter. A decinormal solution contains 1/10 gram equivalent per liter. Normality depends on the amount of solute and temperature. It can be calculated using the formula: Normality = grams of solute x 1000 / (equivalent weight x volume of solution). The normality formula states that the normality of one solution multiplied by its volume equals the normality of a second solution multiplied by its volume. This formula can be used to calculate unknown normalities.
This document provides an overview of buffers in biological systems. It discusses how biological buffers help maintain pH within a narrow physiological range through reversible acid-base reactions. The key types of biological buffers mentioned are bicarbonate, phosphate, proteins, and hemoglobin. Bicarbonate buffers blood pH through reactions involving carbonic acid and carbon dioxide transport. Phosphate buffers intracellular and renal fluid. Proteins and hemoglobin buffer through amino acid side chains that react with hydrogen ions. Maintaining pH is critical for biochemical processes and homeostasis in living organisms.
The document defines pH as the negative logarithm of the hydrogen ion (H+) activity in a solution, with the pH scale ranging from 0 to 14. The hydrogen ions determine if a solution is acidic, alkaline, or neutral - if the hydrogen ion content is measured, the acidity or alkalinity can be determined. Water molecules dissociate into hydrogen and hydroxide ions through autoionization, affecting pH. pH indicators change color depending on the pH of a solution, allowing determination of acidity or alkalinity.
Volumetric analysis involves determining the concentration of a substance by measuring the volume occupied. It is commonly used to determine the unknown concentration of a known reactant through a titration process, where one solution of known concentration and volume is used to react with another substance of unknown concentration until the reaction is complete. The volume of the known solution used is then used to calculate the concentration of the unknown substance. Accuracy in volumetric analysis relies on the use of standardized solutions of primary standards with known concentrations.
Enzymes are proteins that act as biological catalysts, speeding up chemical reactions in cells without being consumed. They are highly specific and can catalyze reactions like metabolism. Enzymes are composed of amino acid chains and sometimes require cofactors to function. They act by binding to substrates at active sites in a lock-and-key or induced fit mechanism. Factors like temperature, pH, concentration of enzymes and substrates affect reaction rates. Enzymes play important roles in the body like digestion, synthesis, degradation of molecules, and protection against pathogens.
Slides giving an overview on pH and its measurement.
Contains information about pH meters, its calibration, maintenance , types of ph electrode and modern definition of pH
This document outlines the procedures and observations for analyzing an unknown salt sample. It describes preliminary examinations to identify possible cations present. It then details systematic analysis of anions using acid and base tests. Specific anions like carbonates, chlorides, acetates and others are tested for. The document concludes by describing analysis of cation groups through precipitation reactions and tests, identifying possibilities like ammonium, lead, copper, aluminum, zinc, barium/strontium/calcium, and magnesium. The goal is to determine the identities of the anions and cations present in the unknown salt.
Osmosis is the net diffusion of water molecules from a dilute solution into a more concentrated solution through a semi-permeable membrane due to a concentration gradient. Osmotic pressure is the excess pressure that must be applied to a solution to prevent the passage of solvent into the solution, and it is measured in units called osmoles. Osmotic pressure follows two laws: πV = nRT and π = cRT, where π is osmotic pressure, V is volume, n is moles of solute, R is the gas constant, T is temperature, and c is molarity. Applications of osmosis include water desalination through reverse osmosis, measuring
This is aimed to explain the isolation of carbohydrates and starch from plant source. To also verify the presence of carbohydrates from the isolation process through several qualitative tests and qualitative tests for monosaccharides, disaccharides and polysaccharides
This document describes a chemistry investigatory project on the digestion of starch by salivary amylase and the effect of temperature and pH. The objectives are to study the digestion of starch by saliva, and the effect of temperature and pH on this process. The required materials and procedures for three experiments are outlined. The first examines the digestion of starch by saliva over time. The second evaluates the effect of temperature on this reaction. The third analyzes how pH impacts salivary amylase activity. The conclusions are that increasing temperature inactivates the enzyme, while it functions best around a pH of 6 to 7.
This document summarizes a protocol for estimating nitrate levels in drinking water. Nitrate testing is important to determine concentrations and ensure they remain below acceptable levels of 10mg/L, as excess nitrate can cause eutrophication and be dangerous to human health, potentially leading to methemoglobinemia or various cancers. The protocol uses sodium chloride, sulfuric acid, brusin sulphanilic acid, and potassium nitrate reagents to oxidize samples in a series of test tubes, which are then read spectrophotometrically to determine nitrate concentrations.
This document discusses the principles and proper use of balances. It explains that a balance measures the force of gravity on an object, or its weight. Weight is dependent on location, while mass remains constant. Electronic balances use electromagnetic forces rather than beams to counterbalance a sample and convert the electrical signal to a weight measurement. The document provides guidelines for operating balances accurately, including leveling, taring, and avoiding sources of error like vibration. It stresses the importance of calibration and quality control programs to ensure balance measurements are valid.
This document describes an experiment to determine the presence or absence of various secondary metabolites in a plant sample. Nine tests were performed to detect phytochemicals like saponins, glycosides, flavonoids, terpenoids, steroids, carotenoids, alkaloids, anthraquinones, and coumarins. Saponins and coumarins were found to be present, while the other phytochemicals were absent based on the observations from the chemical tests. The experiment was aimed at identifying phytochemicals in a given plant and determining which were present.
This document discusses acid-base balance and pH. It defines pH as the negative log of the hydrogen ion concentration. The pH scale ranges from 0 to 14, with values below 7 being acidic and above 7 being basic. The body maintains acid-base balance through buffer systems like bicarbonate and proteins, and respiratory and renal compensation mechanisms. Disturbances in acid-base balance can cause metabolic acidosis, metabolic alkalosis, respiratory acidosis, or respiratory alkalosis.
The document discusses carbohydrate structure and properties. It covers the biological and medical importance of carbohydrates, including their functions as energy stores and structural components. It also describes the chemical nature of carbohydrates as polyhydroxy alcohols with an aldehyde or keto group. Carbohydrate structure is examined using Fisher, Haworth and chair conformations. Carbohydrates are classified as monosaccharides, oligosaccharides like disaccharides, and polysaccharides including homo- and heteropolysaccharides. Important monosaccharides, derivatives, disaccharides and polysaccharides are identified. Properties of monosaccharides such as isomerism, optical activity, epimerism, hemiacetal/ketal formation,
1. Several qualitative tests can identify the presence of carbohydrates, including the Molisch test, iodine test, Benedict's test, Barfoed's test, Seliwanoff's test, and osazone tests.
2. The Molisch test uses alpha-naphthol and sulfuric acid to detect the presence of any carbohydrate, producing a purple ring at the interface. Benedict's test uses copper sulfate and citrate in an alkaline solution to detect reducing sugars based on the color of precipitation.
3. The iodine test detects polysaccharides like starch, producing colors from blue to reddish-brown depending on the type. Barfoed's test distinguishes monos
The document discusses enzymes, substrates, and how they interact. It defines enzymes as proteins that catalyze chemical reactions and substrates as molecules that enzymes act upon. It describes how enzymes and substrates form an enzyme-substrate complex, in which the substrate binds to the active site of the enzyme. This allows the enzyme to catalyze the reaction and convert the substrate into products, before releasing the products and binding with new substrates. The document explores models of enzyme-substrate binding, such as the lock-and-key and induced fit models. It also outlines the four steps of enzyme action and how factors like temperature can regulate enzyme activity.
Sampling in analytical chemistry sajjad ullahSajjad Ullah
Sampling is the process of obtaining representative samples of materials like solids, liquids, and gases. It is a critical step in analysis. For heterogeneous solids, several individual samples are taken and combined into a gross sample. For liquids, grab samples or devices like thieves or impingers are used. Gases can be sampled directly or with enrichment using adsorption tubes, impingers, or chemical reactions. The key steps are sampling, transport, analysis, and assessment. Careful sampling ensures accurate results.
This presentation discusses normality, which is a measure of concentration defined as the number of gram equivalents of solute per liter of solution. A normal solution contains 1 gram equivalent of solute per liter. A decinormal solution contains 1/10 gram equivalent per liter. Normality depends on the amount of solute and temperature. It can be calculated using the formula: Normality = grams of solute x 1000 / (equivalent weight x volume of solution). The normality formula states that the normality of one solution multiplied by its volume equals the normality of a second solution multiplied by its volume. This formula can be used to calculate unknown normalities.
This document provides an overview of buffers in biological systems. It discusses how biological buffers help maintain pH within a narrow physiological range through reversible acid-base reactions. The key types of biological buffers mentioned are bicarbonate, phosphate, proteins, and hemoglobin. Bicarbonate buffers blood pH through reactions involving carbonic acid and carbon dioxide transport. Phosphate buffers intracellular and renal fluid. Proteins and hemoglobin buffer through amino acid side chains that react with hydrogen ions. Maintaining pH is critical for biochemical processes and homeostasis in living organisms.
The document defines pH as the negative logarithm of the hydrogen ion (H+) activity in a solution, with the pH scale ranging from 0 to 14. The hydrogen ions determine if a solution is acidic, alkaline, or neutral - if the hydrogen ion content is measured, the acidity or alkalinity can be determined. Water molecules dissociate into hydrogen and hydroxide ions through autoionization, affecting pH. pH indicators change color depending on the pH of a solution, allowing determination of acidity or alkalinity.
Volumetric analysis involves determining the concentration of a substance by measuring the volume occupied. It is commonly used to determine the unknown concentration of a known reactant through a titration process, where one solution of known concentration and volume is used to react with another substance of unknown concentration until the reaction is complete. The volume of the known solution used is then used to calculate the concentration of the unknown substance. Accuracy in volumetric analysis relies on the use of standardized solutions of primary standards with known concentrations.
Enzymes are proteins that act as biological catalysts, speeding up chemical reactions in cells without being consumed. They are highly specific and can catalyze reactions like metabolism. Enzymes are composed of amino acid chains and sometimes require cofactors to function. They act by binding to substrates at active sites in a lock-and-key or induced fit mechanism. Factors like temperature, pH, concentration of enzymes and substrates affect reaction rates. Enzymes play important roles in the body like digestion, synthesis, degradation of molecules, and protection against pathogens.
Slides giving an overview on pH and its measurement.
Contains information about pH meters, its calibration, maintenance , types of ph electrode and modern definition of pH
This document outlines the procedures and observations for analyzing an unknown salt sample. It describes preliminary examinations to identify possible cations present. It then details systematic analysis of anions using acid and base tests. Specific anions like carbonates, chlorides, acetates and others are tested for. The document concludes by describing analysis of cation groups through precipitation reactions and tests, identifying possibilities like ammonium, lead, copper, aluminum, zinc, barium/strontium/calcium, and magnesium. The goal is to determine the identities of the anions and cations present in the unknown salt.
Osmosis is the net diffusion of water molecules from a dilute solution into a more concentrated solution through a semi-permeable membrane due to a concentration gradient. Osmotic pressure is the excess pressure that must be applied to a solution to prevent the passage of solvent into the solution, and it is measured in units called osmoles. Osmotic pressure follows two laws: πV = nRT and π = cRT, where π is osmotic pressure, V is volume, n is moles of solute, R is the gas constant, T is temperature, and c is molarity. Applications of osmosis include water desalination through reverse osmosis, measuring
This is aimed to explain the isolation of carbohydrates and starch from plant source. To also verify the presence of carbohydrates from the isolation process through several qualitative tests and qualitative tests for monosaccharides, disaccharides and polysaccharides
This document describes a chemistry investigatory project on the digestion of starch by salivary amylase and the effect of temperature and pH. The objectives are to study the digestion of starch by saliva, and the effect of temperature and pH on this process. The required materials and procedures for three experiments are outlined. The first examines the digestion of starch by saliva over time. The second evaluates the effect of temperature on this reaction. The third analyzes how pH impacts salivary amylase activity. The conclusions are that increasing temperature inactivates the enzyme, while it functions best around a pH of 6 to 7.
This is a investigatory project report on the topic of the effects of Salivary amylase on different temperatures and pH. This is a investigatory project report for class 12th biology students of CBSE board or any board.
1) The document is a chemistry project report submitted by Samuel Kumar about studying the digestion of starch by salivary amylase and the effect of temperature and pH on it.
2) Three experiments were conducted to study the digestion of starch by saliva, the effect of temperature on digestion, and the effect of pH on digestion.
3) The results showed that starch is digested by salivary amylase, higher temperatures increase the rate of digestion, and digestion does not occur under acidic or alkaline conditions.
Investigate the effect of temperature on amylase activitylanceqwerty
The document describes an experiment to investigate the effect of temperature on amylase activity. The aim is to determine the reaction rate of amylase and starch solutions at different temperatures (0°C, room temperature, 40°C, 60°C, 80°C). It is hypothesized that the reaction rate will initially increase with temperature until an optimal temperature is reached, above which the enzyme will denature and the rate will decrease. The method involves mixing amylase and starch solutions at the various temperatures and recording the time taken for the blue-black color from iodine solution to disappear. However, the results showed no color change, suggesting a failure of the experimental method.
Investigatory project chemistry on to study the digestion of starch by salivary amylase and effect of temperature and pH on it and
1)To study digestion of starch by saliva.
2)To study the effect of temperature on the digestion of
starch by saliva.
3)To study the effect of pH on the salivary digestion of
starch.
The student investigated how temperature affects the activity of the enzyme catalase. Potato was used as the source of catalase, which breaks down hydrogen peroxide into oxygen gas and water. The experiment found that oxygen production peaked at 38°C, the optimum temperature, and declined at higher and lower temperatures as the enzyme became less active due to changes in kinetic energy and potential denaturing. This supported the hypothesis that enzyme activity is highest near body temperature when the rate of substrate-enzyme collisions is maximized.
This document appears to be a student's chemistry project report on studying the digestion of starch by salivary amylase and the effects of temperature and pH on this process. It includes sections on objectives, introduction, materials, procedures, observations, and conclusions for 3 experiments. The first experiment examines the digestion of starch by saliva over time. The second analyzes the impact of temperature. The third evaluates the impact of pH. The report was guided by a teacher and examines the student's investigation on how salivary amylase breaks down starch at different temperatures and pH levels.
M. Sai Charan completed a chemistry investigatory project on studying the digestion of starch by salivary amylase and the effect of pH and temperature. The objectives were to study starch digestion by saliva and the impact of temperature and pH on the process. Experiments were conducted with starch solution, saliva, iodine solution, and variations in temperature and pH levels. Results showed that salivary amylase digests starch into simpler sugars, and increased temperature inactivated the enzyme while different pH levels also affected digestion. The project fulfilled requirements for the class 12 chemistry practical examination.
The document summarizes a lab report on the effects of pH and concentration on enzyme activity. The introduction provides background on enzymes and their role in catalysis. Four experiments are described that test the effects of enzyme concentration, temperature, pH, and substrate concentration on the reaction rate of catalase. The results show that higher concentrations of enzyme and substrate as well as optimal pH levels increase reaction rate, while higher temperatures and enzyme inhibitors decrease activity. Overall, the objectives of determining how environmental factors influence reaction rates were met.
This document provides instructions for students on proper conduct during an industrial training program. It emphasizes the importance of being on time, paying attention, actively participating, asking questions for clarity, taking notes on difficult concepts, improving listening skills, never neglecting the program, and gaining as much knowledge as possible. It also includes a daily diary template for students to document their training experience.
The document discusses several experiments on factors that affect the rate of chemical reactions:
1. Particle size - Comparing the reaction of dilute HCl with large vs. small marble chips to see how particle size impacts the reaction rate. Smaller particles react faster due to a greater surface area.
2. Catalyst - Adding manganese dioxide speeds up the decomposition of hydrogen peroxide into oxygen and water, showing how a catalyst increases the reaction rate without being used up in the reaction.
3. Temperature - Measuring the time it takes for tablets to dissolve in hot, room temperature, and cold water, demonstrating that higher temperatures increase molecular motion and collision frequency, speeding up reactions.
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The effect of temperature activity of salivary amylase on starch.pdf
1. Chemistry Investigatory
Project
AISSCE 2022-23
Topic:- The effect of
temperature activity of saliva
on starch.
Name : Dev Mandal
Class : XII
Roll no :
Subject and code : Chemistry (043)
Directed by:- Mr. Nishit Kumar Priyadarshi
ODISHA ADARSHA VIDYALAYA
GONDHIPALLY, MALKANGIRI
Pincode:- 764045
2. REFERENCES
1. Chemistry Laboratory Manual of class 12
by NCERT
2. AMRITA Vishwa Vidyapeetham
3.OLABS Education
4. CDAC, Mumbai
5. NCERT at FINGERTIPS (Biology)
class 11 by MTG team.
3. TABLE of CONTENTS
1.Introduction
2.Working of salivary
amylase
3.Effect of Temperature
4.Effect of pH
5.Experiment
5.1 Aim
5.2 Apparatus & Materials
Reqiured
5.3 Theory
5.4 Procedure
5.5 Observations
6. Conclusion
4. Introduction
All living beings need energy to survive. It is
from the food we consume that we get our energy.
We know that the energy we are getting is by
the process of digestion that breaks down the
complex substance of starch into simpler
molecules of glucose, which are further
metabolized into CO2 and water through the
process of glycolysis. The human digestive
tract starts at the mouth and ends at the anus.
Working of Salivary
Amylase
The digestion of the food starts as soon as we
put food in our mouth. Our teeth cut the food
into small pieces and the salivary glands
secrete saliva that mixes with these food
materials. The saliva contains an enzyme called
salivary amylase which hydrolyses starch into
maltose. The saliva secreted into oral cavity
contains electrolytes (Na
+
, K
+
, Cl
-
, HCO3
-
) and
enzymes, salivary amylase and lysozyme The
chemical process of digestion is initiated in
5. Salivary Amylase
pH 6.8
the oral cavity by the hydrolytic action of the
carbohydrate splitting enzyme, the salivary
amylase.
Salivary amylase converts starch into maltose,
isomaltose and small dextrins called '
α' dextrins. About 30 percent of starch in the
food is hydrolysed in the oral cavity. Lysozyme
present in saliva acts as antibacterial agent
that prevents infections.
Starch Maltose + Isomaltose + α-Dextrins
The complete digestion of starch occurs only in
the small intestine by the action of pancreatic
amylase.
The activity of enzymes is strongly affected by
several factors, such as temperature and pH.
6. Effectof Temperature
All enzymes are proteinaceous in nature. At a
lower temperature, the enzyme salivary amylase
is deactivated and at the higher temperature,
the enzyme is denaturated. Therefore, more time
will be taken by an enzyme to digest the starch
at lower and higher temperatures. Optimum
temperature for the enzymatic activity of
salivary amylase ranges from 32 °C to 37 °C.
The optimum temperature means that the
temperature at which the enzyme shows the
maximum activity. At this optimum temperature,
the enzyme is most active and hence, takes less
time to digest the starch.
Effect of pH
The optimum pH for the enzymatic activity of
salivary amylase ranges from 6 to 7. Above and
below this range, the reaction rate reduces as
enzymes get denaturated. The enzyme salivary
amylase is most active at pH 6.8. Our stomach
has high level of acidity which causes the
salivary amylase to denature and change its
shape. So the salivary amylase does not
function once it enters the stomach.
7. Experiment
Aim
In order to study the effect of temperature on
the digestion of starch by saliva
Materials Required
Three series of test tubes having iodine
solution in each, test tubes, ice cubes, water,
15 ml 1% starch solution + 3 ml 1% NaCl, saliva
solution, droppers, thermometer, Bunsen burner
and wire gauze.
Take about 20-30 mL of warm distilled water
(30°C– 40°C) in the mouth and mix it with the
saliva by gargling in the mouth. Collect the
saliva mixed water in a beaker.
Procedure
1. Take 10 mL of the starch solution in a
boiling tube and add 2mL of 1% sodium
chloride solution in it.
2. Keep the boiling tube in a water bath,
maintained at 30° – 40°C, for at least 15
minutes.
3. Pour 2 mL of the saliva solution in the
boiling tube and start the stopwatch
8. immediately.
4. Take out 2-3 drops of the mixture after
one minute and pour it in the test tube
containing iodine solution.
5. Shake the contents of the test tube and
note the colour of the solution, if any.
Similarly, take out 2-3 drops of the
mixture from the boiling tube after every
oneminute and add to iodine solution
contained in the test tubes.
6. Record the colour of the solution in
each case.
7. Stop taking readings when there is no
change in colour.
8. Record the readings in a tabular form.
In order to study the effect of temperature
on the digestion of starch by saliva,
perform the above experiment at 50°C.
9. The effect of pH of reaction medium
can also be studied by using small
quantities of dilute HCl and dilute NaOH in
the separate experiments carried out in the
same manner as above.
Result
The effect of temperature and pH on the
activity of salivary amylase on starch can be
studied by using the Iodine test. If we add
saliva on starch, the salivary amylase present
in saliva gradually acts on starch and converts
it into maltose. Starch keeps on giving blue
colour with iodine till it is completely
digested into maltose. At this point, no blue
colour is formed. This is the end point or
9. achromic point.
It takes less time to reach achromic point at
37°C, as the enzyme is maximum active at this
temperature, while at higher and lower
temperatures more time is taken to reach the
achromic point.
Conclusion
All enzymes are proteinaceous in nature. At
lower temperatures, the enzyme salivary amylase
is deactivated and at higher temperatures, the
enzyme is denaturated. Therefore, more time
will be taken by enzyme to digest the starch at
lower and higher temperatures. At 37° C, the
enzyme is most active, hence, takes less time
to digest the starch.
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