Ampicillin resistant Native promoter Wild type enzyme 5’5’3’3’ HindIII Start Codon Stop Codon BsteII phoA in pEK8.

Slides:



Advertisements
Similar presentations
Useful hints and tips for cloning, PCR and site-directed mutagenesis
Advertisements

Plasmids, primers (and beyond!). Or how to make green mice….
Cell-free Bacterial Yeast Insect Mammalian Protein Expression Systems.
Predicting Genes in Mycobacteriophages December 8, In Silico Workshop Training D. Jacobs-Sera.
Genome Scale PCR Infidelity Search Goal: An efficient search for the presence of potential undesired PCR products that scans through 3 billion bases of.
DNA Science Day 1 Amplifying and Cutting APh162 Winter 2005 Caltech.
Single DNA Sequence Analysis Tools BME 110: CompBio Tools Todd Lowe May 6, 2008.
Plasmid Construction and Purification of Arabidopsis Plantacyanin and Lily Chemocyanin in a Prokaryotic System Suhyen Lee and Brooke Vuong (Aram Nersissian)
Genetics in the real world: Developing a new genetic system in bacteria Abigail Salyers
Sequence Analysis. DNA and Protein sequences are biological information that are well suited for computer analysis Fundamental Axiom: homologous sequences.
Primer design for PCR cloning special case for when the insert is to be cloned PCR also used for diagnostic (is gene present) PCR also used to quantitate.
Lecture 1 Introduction to recombinant DNA Technology Dr Muhammad Imran.
Genetic transformation of E. coli bacteria
Nucleic Acid Secondarily Structure AND Primer Selection Bioinformatics
Application in Molecular Cloning David Shiuan Department of Life Science, Institute of Biotechnology and Interdisciplinary Program of Bioinformatics National.
The glycerol kinase gene (glpK) of M. pneumoniae contains 10 TGA codons Idea: changing simultaneously all the TGA codons into TGG codons (TGG = tryptophan.
Biological Dynamics Group Central Dogma: DNA->RNA->Protein.
Enzymes Used for Gene Engineering 1. Restriction endonuclease (restriction enzymes) 2. DNA modifying enzymes a polymerases b nucleases c enzymes that modify.
ATGGCAAAAGATCGTCGCAGTAATGAAGCTGAAAATATCGCTGTTGTTGAAAAACCGCTGAAATCGGACCG CTTCTTTA TCTCTGATGGTCTGCCGAGTCCGTTCGGCCCGACCGTTCGTGATGACGGTGTGAATTTTTCTGTTTATAGT.
Location of features Human cytomegalovirus (CMV) immediate early promoter: 1–589 Enhancer region: 59–465; TATA box: 554–560; Transcription start point:
Watermarks.  Four sequences, 1000 bp each  Inserted into noncoding regions of genome  Translated into English using secret triplet nucleotide to character.
BME 110L / BIOL 181L Computational Biology Tools October 29: Quickly that demo: how to align a protein family (10/27)
Laboratory for Molecular and Computational Genomics Optical Mapping of E-coli O157:H7 Alex Lim.
Doug Raiford Lesson 3.  Have a fully sequenced genome  How identify the genes?  What do we know so far? 10/13/20152Gene Prediction.
BME 110L / BIOL 181L Computational Biology Tools February 19: In-class exercise: a phylogenetic tree for that.
A.B. C. orf60(pOrf60) 042orf orf60(pOrf60-M5 ) orf60(pOrf60-M1) orf60(pOrf60-M4) 042orf60 042orf60(pOrf60-M5) orf60(pOrf60) 042orf60(pOrf60-M1)
Molecular Genetics Lab Review. Bacterial Transformation Genetic transformation—host organism takes in and expresses foreign DNA Genetic engineering—manipulation.

Part 2: Molecular Biology IGEM, 20 June Proteins Structural and catalytic components of cells are mainly proteins. Linear polymers of 20 different.
Biotechnology biotechnology – manipulation of biological organisms (usually with DNA itself) To study the functions of individual genes, molecular biologists.
Recombinant DNA What is the basis of recombinant DNA technology? How does one “clone” a gene? How are genetically modified organisms (GMOs) created? Illustration.
Essential Basic Part Types Coding Sequences (C) - Complete open reading frames (type I), or sequences encoding polypeptides but lacking either a stop codon.
Doug Raiford Lesson 2.  Material of life  Heritable traits  The job of DNA is to produce proteins  Involved in virtually every chemical reaction ▪
Question: How do we know where a particular protein
 What is different between these 2 sequences? GGAATTCCTAGCAAT CCTTAAGGATCGTTA CTACGTGAGGAATTC GATGCACTCCTTAAG.
Microbial Structure and Function MI720 Fall 2007 DNA Recombination Andrew J. Pierce Department of Microbiology, Immunology and Molecular Genetics University.
 Test Review Lecturer: David Mendez. But first  Take out a sheet of paper.
Primer on Reading Frames and Phase Wilson Leung08/2012.
What can you do with DNA? Chapter 8. Success Criteria At the end of class today, you will be able to: Explain what a restriction enzyme is and what role.
Sanger Method Frederick Sanger Radioactively labelled dNTPs or radioactive/fluorescent primers  Autoradiography, laser detector Chain Termination.
Fantasy Mutations Reality. Mutations: a permanent and heritable change in the nucleotide sequence of a gene. Are caused by mutagens (x-rays and UV light)
TOOLS OF GENETIC ENGINEERING. There are a number of tools used in genetic engineering. One of them are enzymes.
Lecture 7 January 16, 2016 Biotech 3.
Question: How do we know where a particular protein is located in the cell?
Protein Expression Systems
bacteria and eukaryotes
Topics to be covers Basic features present on plasmids
“How does it affect the protein?”
PCR Polymerase Chain Reaction
Creating Transgenic Synechococcus elongatus
New vector designs for expression and general-purpose vectors.
Biotech Tools Review
Step 1: amplification and cloning procedures
Gene Editing Design Demo
Yeast Cryptography: A Budding New Way to Keep Your Dough
Predicting Genes in Actinobacteriophages
Structure of in‐frame deletions.
Rationale for generation of reporter fusions by Red-mediated recombination. Rationale for generation of reporter fusions by Red-mediated recombination.
Determine the Identity of Unknown Plasmids
What do you with a whole genome sequence?
High rates of antibiotic resistance among normal fecal flora Escherichia coli isolates in children from Greece  A.C. Vatopoulos, E. Varvaresou, E. Petridou,
Python.
The Complete Genome Sequence of Escherichia coli K-12
Volume 154, Issue 6, Pages (September 2013)
Reading Frames and ORF’s
Tagging of the endogenous Py03652 gene with the gfp gene in Plasmodium yoelii. Tagging of the endogenous Py03652 gene with the gfp gene in Plasmodium yoelii.
Southern blot analysis of ΔpksP mutant generated in the Af293 background. Southern blot analysis of ΔpksP mutant generated in the Af293 background. (A)
Relationship between Genotype and Phenotype
Editing of ADE2 in C. metapsilosis.
Presentation transcript:

Ampicillin resistant Native promoter Wild type enzyme 5’5’3’3’ HindIII Start Codon Stop Codon BsteII phoA in pEK8

Potential New Plasmids

pET29a 5’5’3’3’ HindIII Start Codon Stop Codon BsteII

pET29a

We want a C-terminal histidine tag We do not want an S-Tag 5’5’ 3’3’ HindIII Start Codon Stop Codon BsteII

We want a C-terminal histidine tag We do not want an S-Tag New TAA Stop codon 5’5’ 3’3’ HindIII Start Codon Stop Codon BsteII 5’5’ 3’3’ HindIII Start Codon Stop Codon BsteII NdeIXhoI

phoA Primer Design Find the sequence of phoA in pEK48 Append new endonuclease cut sites Delete the stop codon Do some tinkering with Tm and ends

phoA Sequence Expasy Translate TTGTCACGGCCGAGACTTATAGTCGCTTTG TTTTTATTTTTTAATGTATTTGTACATGGAGAAAATAAAGTGAAACAAAGCAC TATTGCACTGGCACTCTTACCGTTACTGTTTACCCCTGTGACAAAAGCCCGGACACCAGAAATGCCTGTTCTGGAAAACCGGGCTGCTCAGGGCGATATTAC TGCACCCGGCGGTGCTCGCCGTTTAACGGGTGATCAGACTGCCGCTCTGCGTGATTCTCTTAGCGATAAACCTGCAAAAAATATTATTTTGCTGATTGGCGAT GGGATGGGGGACTCGGAAATTACTGCCGCACGTAATTATGCCGAAGGTGCGGGCGGCTTTTTTAAAGGTATAGATGCCTTACCGCTTACCGGGCAATACACT CACTATGCGCTGAATAAAAAAACCGGCAAACCGGACTACGTCACCGACTCGGCTGCATCAGCAACCGCCTGGTCAACCGGTGTCAAAACCTATAACGGCGC GCTGGGCGTCGATATTCACGAAAAAGATCACCCAACGATTCTGGAAATGGCAAAAGCCGCAGGTCTGGCGACCGGTAACGTTTCTACCGCAGAGTTGCAG GATGCCACGCCCGCTGCGCTGGTGGCACATGTGACCTCGCGCAAATGCTACGGTCCGAGCGCGACCAGTGAAAAATGTCCGGGTAACGCTCTGGAAAAA GGCGGAAAAGGATCGATTACCGAACAGCTGCTTAACGCTCGTGCCGACGTTACGCTTGGCGGCGGCGCAAAAACCTTTGCTGAAACGGCAACCGCTGGTG AATGGCAGGGAAAAACGCTGCGTGAACAGGCACAGGCGCGTGGTTATCAGTTGGTGAGCGATGCTGCCTCACTGAATTCGGTGACGGAAGCGAATCAGCA AAAACCCCTGCTTGGCCTGTTTGCTGACGGCAATATGCCAGTGCGCTGGCTAGGACCGAAAGCAACGTACCATGGCAATATCGATAAGCCCGCAGTCACCT GTACGCCAAATCCGCAACGTAATGACAGTGTACCAACCCTGGCGCAGATGACCGACAAAGCCATTGAATTGTTGAGTAAAAATGAGAAAGGCTTTTTCCTGC AAGTTGAAGGTGCGTCAATCGATAAACAGGATCATGCTGCGAATCCTTGTGGGCAAATTGGCGAGACGGTCGATCTCGATGAAGCCGTACAACGGGCGCTG GAATTCGCTAAAAAGGAGGGTAACACGCTGGTCATAGTCACCGCTGATCACGCCCACGCCAGCCAGATTGTTGCGCCGGATACCAAAGCTCCGGGCCTCA CCCAGGCGCTAAATACCAAAGATGGCGCAGTGATGGTGATGAGTTACGGGAACTCCGAAGAGGATTCACAAGAACATACCGGCAGTCAGTTGCGTATTGCG GCGTATGGCCCGCATGCCGCCAATGTTGTTGGACTGACCGACCAG ACCGATCTCTTCTACACCATGAAAGCCGCTCT GGGGCTGAAATAA E. coli strain K-12 bases NCBI BLAST

E. coli K-12 Start Codons 4288 open reading frames 3542 start with ATG, 83% methionine 612 start with GTG, 14% valine 130 start with TTG, 3% luecine Blattner FR, Plunkett G 3rd, Bloch CA, Perna NT, Burland V, Riley M, Collado-Vides J, Glasner JD, Rode CK, Mayhew GF, Gregor J, Davis NW, Kirkpatrick HA, Goeden MA, Rose DJ, Mau B, Shao Y. The complete genome sequence of Escherichia coli K-12. Science Sep 5 277(5331):

Forward Primer NdeI 5’ TTGAUGTCACGGCCGAGACTTATAGTCGCTTTG 5’ CATATGAUGTCACGGCCGAGACTTATAGTCGCTTTG 5’ AAAAAAAACATATGAUGTCACGGCCGAGACTTATAGTCGCTT TG

Reverse Primer XhoI Reverse and complement 5’ ACCGATCTCTTCTACACCATGAAAGCCGCTCTGGGGCTGAAATA A 5’ ACCGATCTCTTCTACACCATGAAAGCCGCTCTGGGGCTGAAACTCGAG 5’AAAAAAAACTCGAGTTTCAGCCCCAGAGCGGCTTTCATGGTGTAGAAGAGATCGGT 5’ ACCGATCTCTTCTACACCATGAAAGCCGCTCTGGGGCTGAAACTCGAGTTTT TTTT

Melting Temperature Melting temperature to be between 55 and 60 C Melting temperatures to be as close to one another as possible Melting Temperature Calculator

pASK IBA 43+