Lab 5: Cellular Respiration

Slides:



Advertisements
Similar presentations
Review of AP Laboratories
Advertisements

Lab 3: Mitosis & Meiosis Conclusions Mitosis Meiosis
SL Biology Unit #6 Biotech
Biotechnology Chapter 11.
AP Biology Lab Review.
Lab 6: Molecular Biology Description – Gel electrophoresis cut DNA with restriction enzyme fragments separate on gel based on size.
AP Biology Lab Review.
Genetic engineering ­ Genetic engineering: manipulating DNA or organisms to perform practical tasks or provide useful products We’re going to look at the.
TOOLS OF GENETIC ENGINEERING
Ch. 13 Genetic Engineering
Genetic Engineering. We can use a process called gel electrophoresis to separate the pieces.
Chapter 20: Biotechnology. Essential Knowledge u 3.a.1 – DNA, and in some cases RNA, is the primary source of heritable information (20.1 & 20.2)
CHAPTER 20 BIOTECHNOLOGY: PART I. BIOTECHNOLOGY Biotechnology – the manipulation of organisms or their components to make useful products Biotechnology.
Lab Review: 1-6 AP Biology Lab Review Lab 1: Diffusion & Osmosis.
AP Biology Lab Review.
Chapter 20~DNA Technology & Genomics. Who am I? Recombinant DNA n Def: DNA in which genes from 2 different sources are linked n Genetic engineering:
distance from centromere
Genetic Engineering. Genetic Engineering: Genetic Engineering: process of altering biological systems by the purposeful manipulation of DNA Applications:
Section 2 Genetics and Biotechnology DNA Technology
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Genetic Engineering. What is genetic engineering? Application of molecular genetics for practical purposes Used to – identify genes for specific traits.
Class Notes 1: DNA Manipulation. I. DNA manipulation A. During recent years, scientists have developed a technique to manipulate DNA, enabling them to.
Manipulation of DNA. Restriction enzymes are used to cut DNA into smaller fragments. Different restriction enzymes recognize and cut different DNA sequences.
AP Biology Lab Review Girard AP Biology Lab 1: Diffusion & Osmosis.
Genetic Engineering Chapter 13 Recombinant DNA Transformation Biotechnology Gel Electrophoresis PCR.
Overview Amgen Biotech Labs In this set of labs, students will:
Genetics 6: Techniques for Producing and Analyzing DNA.
19.1 Techniques of Molecular Genetics Have Revolutionized Biology
Review from last week. The Making of a Plasmid Plasmid: - a small circular piece of extra-chromosomal bacterial DNA, able to replicate - bacteria exchange.
L AB 6: M OLECULAR B IOLOGY L AB 6: M OLECULAR B IOLOGY Description Transformation insert foreign gene in bacteria by using engineered plasmid.
DNA Technology Chapter 11. Genetic Technology- Terms to Know Genetic engineering- Genetic engineering- Recombinant DNA- DNA made from 2 or more organisms.
Post-Lab Analysis Cellular Respiration. 1. What gas is being consumed by the germinating pea?  oxygen.
Lab 5: Cellular Respiration Lab 5: Cellular Respiration Description ◦ using respirometer to measure rate of O 2 production by pea seeds 
Effects of Germination and Temperature on Respiration Rate
Desired Gene Restriction Enzymes Bacterial defense against viral DNA Bacterial defense against viral DNA Cut DNA at specific sequences Cut DNA at specific.
Researchers use genetic engineering to manipulate DNA. Section 2: DNA Technology K What I Know W What I Want to Find Out L What I Learned.
Manipulating DNA. Scientists use their knowledge of the structure of DNA and its chemical properties to study and change DNA molecules Different techniques.
Chapter 20: DNA Technology and Genomics - Lots of different techniques - Many used in combination with each other - Uses information from every chapter.
Biology Chapter 9 & Honors Biology Chapter 13 Frontiers Of Biotechnology.
DNA Technology Ch. 20. The Human Genome The human genome has over 3 billion base pairs 97% does not code for proteins Called “Junk DNA” or “Noncoding.
Vocab review Unit 8 - biotechnology. 1. Organism that has acquired genetic material by artificial means.
Difficulties with DNA 1. 1.One cell normally provides too little material for study Gene cloning Polymerase Chain Reaction (PCR) 2. 2.There are often.
AP Biology Lab Review AP Biology  Description  To breed Wisconsin Fast Plants for three generations and carry-out artificial selection for plants with.
- making changes to the DNA code of a living organism.
Biotechnology.
Recombinant DNA Technology
21.8 Recombinant DNA DNA can be used in
Chapter 14.3 & 15 Biotechnology
Section 2 Genetics and Biotechnology DNA Technology
Chapter 20: DNA Technology and Genomics
Restriction Enzymes and Plasmid Mapping
DNA Technology Now it gets real…..
and PowerPoint “DNA Technology,” from
the manipulation of living organisms for human use Chapter 13
Biotechnology EOC review
5. Genetic Engineering Techniques
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
DNA Technology.
The student is expected to: (6H) describe how techniques such as DNA fingerprinting, genetic modifications, and chromosomal analysis are used to study.
Biotechnology.
Recombinant DNA Unit 12 Lesson 2.
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
AP Biology Lab Review.
Genetics and Biotechnology
Genetics and Biotechnology
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Chapter 20: DNA Technology and Genomics
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Genetic Engineering.
KEY CONCEPT Biotechnology relies on cutting DNA at specific places.
Presentation transcript:

Lab 5: Cellular Respiration

Lab 5: Cellular Respiration Description using respirometer to measure rate of O2 production by pea seeds non-germinating peas germinating peas effect of temperature control for changes in pressure & temperature in room

Lab 5: Cellular Respiration Concepts respiration experimental design control vs. experimental function of KOH function of vial with only glass beads

Lab 5: Cellular Respiration Conclusions temp = respiration germination = respiration calculate rate?

Lab 5: Cellular Respiration ESSAY The results below are measurements of cumulative oxygen consumption by germinating and dry seeds. Gas volume measurements were corrected for changes in temperature and pressure. a. Plot the results for the germinating seeds at 22°C and 10°C. b. Calculate the rate of oxygen consumption for the germinating seeds at 22°C, using the time interval between 10 and 20 minutes. c. Account for the differences in oxygen consumption observed between: 1. germinating seeds at 22°C and at 10°C 2. germinating seeds and dry seeds. d. Describe the essential features of an experimental apparatus that could be used to measure oxygen consumption by a small organism. Explain why each of these features is necessary. Cumulative Oxygen Consumed (mL) Time (minutes) 10 20 30 40 Germinating seeds 22°C 0.0 8.8 16.0 23.7 32.0 Dry Seeds (non-germinating) 22°C 0.2 0.1 Germinating Seeds 10°C 2.9 6.2 9.4 12.5 Dry Seeds (non-germinating) 10°C

Lab 6: Molecular Biology

Lab 6: Molecular Biology Description Transformation insert foreign gene in bacteria by using engineered plasmid also insert ampicillin resistant gene on same plasmid as selectable marker Gel electrophoresis cut DNA with restriction enzyme fragments separate on gel based on size

Lab 6: Molecular Biology Concepts transformation plasmid selectable marker ampicillin resistance restriction enzyme gel electrophoresis DNA is negatively charged smaller fragments travel faster

Lab 6: Transformation Conclusions can insert foreign DNA using vector ampicillin becomes selecting agent no transformation = no growth on amp+ plate

Lab 6: Gel Electrophoresis Conclusions DNA = negatively charged correlate distance to size smaller fragments travel faster & therefore farther

Lab 6: Molecular Biology ESSAY The diagram below shows a segment of DNA with a total length of 4,900 base pairs. The arrows indicate reaction sites for two restriction enzymes (enzyme X and enzyme Y). Explain how the principles of gel electrophoresis allow for the separation of DNA fragments Describe the results you would expect from electrophoretic separation of fragments from the following treatments of the DNA segment above. Assume that the digestion occurred under appropriate conditions and went to completion. DNA digested with only enzyme X DNA digested with only enzyme Y DNA digested with enzyme X and enzyme Y combined Undigested DNA Explain both of the following: The mechanism of action of restriction enzymes The different results you would expect if a mutation occurred at the recognition site for enzyme Y.

Lab 6: Molecular Biology ESSAY The human genome illustrates both continuity and change. Describe the essential features of two of the procedures/techniques below. For each of the procedures/techniques you describe, explain how its application contributes to understanding genetics. The use of a bacterial plasmid to clone and sequence a human gene Polymerase chain reaction (PCR) Restriction fragment polymorphism (RFLP analysis) All humans are nearly identical genetically in coding sequences and have many proteins that are identical in structure and function. Nevertheless, each human has a unique DNA fingerprint. Explain this apparent contradiction.