Question

How could have E. coli be used to aid in the cloning of the bioluminescence genes...

How could have E. coli be used to aid in the cloning of the bioluminescence genes from Vibrio fischeri?
Gene fragments from E. coli were used to disrupt the bioluminescence genes of V. fischeri by homologous recombination.
Gene fragments from V. fischeri were cloned into plasmids, transformed into E. coli, and then retransformed back into V. fischeri.
Transposons from E. coli were used to mutagenize the bioluminescence genes of V. fischeri.
Gene fragments from V. fischeri were transformed into E. coli and bioluminescent E. coli were identified.

Homework Answers

Answer #1

ANSWER :- d.) gene fragments of V.fischeri were transforned into E.coli and bioluminescent E.coli were identified.

The bacteria Vibrio fischeri aremotile, gram negative rod shaped cells that has the ability to produce bioluminescence and was controlled by lux operon, that consist genes that encode for enzyme luciferase (luxAB) and enzyme luxCDE that convert compound in to oxidizable subsrate.

These genes as show bioluminscence will be cloned by using the technique recombinant DNA technology (RDT), so, for that the isolated gene fragments ( Encoding LUX genes ), from V. fischeri were transformed in to E.coli using the plasmid ( extracellular circular DNA ), the recombinant gene ( or cloned genes )  is being identified in to the E.coli cells by bioluminescent.  

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Describe how you would identify genes responsible for transcription in E. coli by isolating mutations in...
Describe how you would identify genes responsible for transcription in E. coli by isolating mutations in their genes. Remember that these genes are required for cell viability. Include all the steps in the isolation of the mutants and also describe how you will differentiate the mutants you want from those in other genes necessary for viability. This includes giving me the expected result for mutants in the genes you want.
You are studying a mouse gene named MtoA. You know that the protein product of this...
You are studying a mouse gene named MtoA. You know that the protein product of this gene localizes to mitochondria in mice. Your goal is that you want to know whether mouse MtoA protein is capable of localizing to mitochondria if produced in yeast cells. You decide to clone a gene into a translational fusion vector that will add jellyfish DNA sequence encoding the GFP proteins (238 amino acids) in place of the normal stop codon. Unfortunately, you can't find...
A theoretical operon (amo) in E. coli contains several structural genes encoding enzymes involved in the...
A theoretical operon (amo) in E. coli contains several structural genes encoding enzymes involved in the biosynthesis of a particular amino acid. Unlike the lac operon, in which the repressor gene is separate from the operon itself, for the amo operon, the repressor gene is found within the operon itself. When the end product amino acid is present, it binds to the repressor, and this complex binds to the operator, repressing the operon. In the absence of the amino acid,...
1. Currently you are studying threonine synthesis in E. coli. To find genes whose protein products...
1. Currently you are studying threonine synthesis in E. coli. To find genes whose protein products are important for threonine synthesis, you perform a mutagenesis to find mutants that require a source of threonine to grow. (a) Immediately after mutagenizing the bacteria, would you choose to grow the bacteria on rich media or on minimal media? Briefly explain your choice. Rich media. A mutant unable to make a particular amino acid will not be able to grown on media lacking...
E. coli is a gram negative organism. S. Epidermidis is a gram positive organism. How could...
E. coli is a gram negative organism. S. Epidermidis is a gram positive organism. How could that information help explain your results? This is for an osmotic pressure lab. E.coli showed the most growth (appeared cloudy) in a 0% NaCl nutrient broth tube. S. Epidermidis also showed the most growth in 0% NaCl, though appeared to have almost no change at all from original nutrient broth tube.
In the experiment, Okazaki cultured E. coli (at low temperatues to slow down replication process) in...
In the experiment, Okazaki cultured E. coli (at low temperatues to slow down replication process) in the presence of radioactive nucleotides. They did this for short pulses followed by the addition of excess nonradioactive nucleotides. This resulted in label (radioactivity) being present only in the DNA that was synthesized during the short period of the pulse. Soon after the pulse, they isolated the DNA and separated the individual strands from one another. The various pieces of DNA could then be...
In theory, cloning could produce: a copy of you Several copies of a gene a forest...
In theory, cloning could produce: a copy of you Several copies of a gene a forest of identical trees All of the above Polymerase chain reaction produces: a southern blot YAC’s Multiple copies of DNA Endonucleases Organisms which carry genetic information into a host cell is called a/an: Vector Probe Endonuclease YAC Testing a fetus in the womb for Cystic fibrosis is an example of: Preimplantation testing Prenatal testing Presymptomatic testing In-vitro testing The alternative to using plasmids for large...
1.A technique used to identify RNA after gel electrophoresis and which employs ssDNA in the detection...
1.A technique used to identify RNA after gel electrophoresis and which employs ssDNA in the detection process is the _____ blot. Select one: a. Northern b. Western c. Northeastern d. Southern e. Southwestern 2. DNA sequencing by controlled termination of replication is called the _____ method. Select one: a. Sanger b. E. coli c. Restriction enzymes d. DNA Microarray e. Ligase f. Polymerase Chain Reaction g. Footprint h. Reverse Trancriptase i. Vector j. Expression k. Fluorescent l. cDNA 3. How...
1). What were the justifications given for funding the Human Genome Project? A). Scientific discoveries B)....
1). What were the justifications given for funding the Human Genome Project? A). Scientific discoveries B). Facilitate technological advances C). Understanding and treating human diseases D). Economic impact E). All of the above. 2). What are some of the concerns with using transcriptional Fusion reporter gene constructs to following the expression of the gene of Interest? A ). The reporter gene fused to the gene of Interest may interfere with the proper folding and function of protein product of the...
1. What would happen to the white blood cells if they were extracted in anything other...
1. What would happen to the white blood cells if they were extracted in anything other than isotonic conditions? Describe what would happen to the cheek cells in hypertonic and hypotonic solutions respectively. 2. The polymerase chain reaction can only be used to amplify genes that have already been cloned and sequenced. Why is this true? 3. If you started a PCR protocol with 10 double-stranded molecules of DNA, how many double-stranded molecules of the product would you have after...