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Microbial Genetics. Biotechnology. A Study of Genetics. Genetics The science of heredity that is concerned with: Transmission of characteristics The nature and function of DNA Patterns of heredity variation within populations and the changes in these patterns. Before we knew about DNA…
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Microbial Genetics Biotechnology
A Study of Genetics Genetics The science of heredity that is concerned with: • Transmission of characteristics • The nature and function of DNA • Patterns of heredity variation within populations and the changes in these patterns.
Before we knew about DNA… You observe that children look similar to their parents, families share characteristics, but often there are new traits that are created. You’ve never heard of DNA, cells, genes… How do you explain inheritance?
Gregor Mendel Charles Darwin Mid 1800s inheritance of Natural Selection genetic traits
Miescher 1869 • Isolated something he called ‘Nuclein’ from white blood cells • Determined that it was composed of: • Sugar, phosphate, and nitrogen • Found that it was weakly acidic • Renamed this substance: Nucleic Acid “DNA Extraction”
1940s • Chromosomes are made of DNA and proteins • Chromosomes carried our hereditary material • Didn’t know if the proteins or the DNA was the hereditary material • Protein was considered most likely because of its complexity and diversity • DNA is only: sugar, phosphate, nitrogen and 4 bases • Protein is combinations of 20 amino acids
1944 Griffiths’ Experiment(utilized Streptococcus pneumoniae) Avirulent strain grows as rough colonies Virulent strain grows as smooth colonies
Griffiths’ Experiment Continued PROVED THAT TRAITS ARE TRANSFERRED FROM ORGANISM TO ORGANISM
Griffiths Summary • R cells avirulent, S Cells virulent • Heat-killed S cells avirulent • [R cells (avirulents) + Heat-killed S Cells (avirulent) = VIRULENCE • Live S cells in blood • Transfer of some substance from dead S cells to live R cells • “Transforming Principle” Traits can be transferred from one organism to another!
Hershey-Chase Experiment • Grew bacteria in presence of either radioactive sulfur (35S) to label proteins (methionine and cysteine) or radioactive Phosphorous (32P) to label DNA • Infected with bacteriophage, let growth and lysis occur, bacteriaphage particles now labeled with 35S or 32P
Evidence that DNA is the hereditary Material Remember: 35S labeled protein 32P labeled DNA
1953 Watson, Crick and Franklin
Two types of Nucleic AcidDNA: deoxyribonucleic acid RNA: ribonucleic acid Both are polymers of nucleotides: P Base Sugar Nucleotide
DNA • 5 carbon deoxyribose sugar • Four bases:
RNA • 5 carbon ribose sugar • Single stranded (ss) • Four Bases:
The DNA Double Helix Sugar phosphate backbone Nitrogenous bases
Right Handed Helix Major groove Minor groove Proteins fit into these grooves when they interact
Purines and Pyrimidines Double ring structures Single ring structures
Base pairing
Joining Nucleotides • Nucleotides grow by addition to the 3’ carbon (the 3’ end) • 3’-5’ phosphate bond
Writing DNA Sequences DNA is always written in the 5’ to 3’ direction: 5’ 3’ 5’ ATCCGCTAACTTAGGCTTACG 3’ Abbreviate the nucleotides by using the first letter of each base
DS DNA Antiparallel 5’ ATCCGACTATCGCGGAAT 3’ 3’ TAGGCTGATAGCGCCTTA 5’ Complimentary Bases A=T (double bond) C=G (triple bond, stronger bond) Two bases joined together is a Base Pair
New DNA New DNA
DNA Replication is a Semi-conservative process
Matching of DNA Bases in DNA Replication 5’ 3’ ATTCGATCTAG 5’ 3’ A G T A G C T A A T C
Requirements for DNA Replication • Template DNA • A, T, C, G Nucleotides • DNA polymerase • primers • Ligase • Helicase
Steps in Replication • Unwinding of the double helix- Helicase • Synthesis of short RNA sequences called Primers on lagging strand • DNA polymerase adds bases onto the 3’ end of the primers • Proofreading • Ligase forms covalent bonds between nucleotides from lagging strand segments
Half of a replication bubble is a replication fork DNA Replication can be bidirectional in bacteria Replication fork Replication fork
The Central Dogma DNA mRNA Protein
DNA DNA DNA mRNA Protein Transcription Replication Translation
Types of RNA Used in Translation • rRNA • Ribosomal RNA, 2 subunits join to make one functional rRNA • tRNA • Transfer RNA, clover leaf shape, carries amino acids to the growing amino acid chain Amino acid attaches here Anticodon Attaches to mRNA
Amino Acids (A.A.) • A chain of amino acids = a protein • There are 20 different amino acids • They have an amino (NH2) group and a carboxyl (COOH) group • The basic structure for an amino acid is at right. A different element or group of elements is in place of the R, this is what makes each A.A. different Amino group (N terminal end) Carboxyl group (C terminal end)
The Steps of TranslationmRNA Amino Acid chain=protein) • Initiation • Elongation • Termination Codon: every 3 bases = a codon=1 amino acid 5’ AUGCGCCGAUUCAGA 3’ The Start codon establishes the Reading Frame
Step 1: Initiation • The ribosome attaches near the 5’ end of the mRNA at the Start Codon AUG AUG codes for the amino acid, Methionine (Met) 5’ AUGCGCCGAUUCAGAACGUUCGA 3’ Multiple ribosomes can attach to an mRNA strand at any one time
Step 2: Elongation 5’ AUGCGCCGAUUCUGAACGUUCGA 3’ AAG UAC Phe GCG GCU CUA Met Arg Arg Asp
Step 2: Elongation cont. 5’ AUGCGCCGAUUCUGAACGUUCGA 3’ UAC GCG AAG GCU Met Arg Phe Arg Only 2 tRNAs can be attached to the mRNA at any one time
Step 2: Elongation cont. 5’ AUGCGCCGAUAAUGAACGUUCGA 3’ GCU GCG AAG Met Arg Arg Phe
Step 3: Termination • Stop codons AUGCGCCGAUUCUGAACGUUCGA 3’
Mutation • Change in the genetic material • Mutations may be neutral, beneficial, or harmful • Mutagen: Agent that causes mutations • Spontaneous mutations: Occur in the absence of a mutagen
Mutation • Change in one base • Result in change in amino acid • Base substitution (point mutation) • Missense mutation Figure 8.17a, b
Mutation • Results in a nonsense codon • Nonsense mutation Figure 8.17a, c
Mutation • Insertion or deletion of one or more nucleotide pairs • Frameshift mutation Figure 8.17a, d
Mutation • Ionizing radiation (X rays and gamma rays) causes the formation of ions that can react with nucleotides and the deoxyribose-phosphate backbone. • Nucleotide excision repairs mutations
Mutation • UV radiation causes thymine dimers • Light-repair separates thymine dimers Figure 8.20