You successfully inserted a foreign piece of DNA, e.g.
the gene for human erythropoetin (EPO), into a bacterial plasmid,
which also contains a gene conferring antibiotic resistance to
ampicillin. What is your next step you do on the way to finally
produce the human hormone in E.coli?
A) you cut the plasmid with restriction enzymes
B) you grow E.coli on agar plates containing ampicillin
C) you grow E.coli on agar plates containing tetracycline
D) you insert the recombinant plasmid into E.coli, i.e. you
transform E.coli
E) you grow E.coli on agar plates containing ampicillin
Ans:The next step in the recombinant DNA technology is always transferring this recombinant plasmid to host i.e bacteria E.coli so option D is correct.
After that transfer the bacteria containing the recombinant would be allowed to grow on Agar plate containing ampicillin.
You successfully inserted a foreign piece of DNA, e.g. the gene for human erythropoetin (EPO), into...
Which statement about gene cloning is false? A. Bacterial cells take up recombinant plasmids by transformation. B. Recombinant DNA molecules usually contain a DNA fragment inserted into a bacterial vector. C. To insert a gene of interest into a vector, the gene of interest and the vector must be digested with different restriction enzymes D. Transformed bacteria are plated onto media containing the appropriate antibiotic and only bacteria containing the plasmid with antibiotic resistance will grow.
RECOMBINANT DNA: PLASMID VECTOR engineering is the direct manipulation of an organism's DNA using nology. To begin the recombinant DNA process, scientists must first ide at codes for the production of the protein they want to manufacture. One is to go backwards from the amino acid sequence of the desired protein to ide sequence of the gene. After scientists have identified the gene, they m it. Restriction enzymes or endonucleases from bacterial cells are key in th ia produce restriction...
The bacterial containing the plasmid with the gene of interest successfully inserted in would grow in A. The nutrient broth only B. The nutrient broth, the ampicillin broth, and the tetracyclin broth. C. The nutrient broth and the tetracyclin broth only D. The ampicillin broth and nutient broth E. The ampicillin and tetracyclin broth only Which one and why?
the genetic blueprint of an organism is referred to as i
A scientist wishes to genetically engineer E. coli bacteria so that it will contain the green fluorescent protein (GFP) gene. Which of the following protocol outlines would the scientist use to accomplish this task? ОА Insert GFP gene into corn expression cassette; insert expression cassette into plasmid vector; insert plasmid vector into Agrobacterium tumefaciens bacteria; allow bacteria to infect corn plant; GFP gene inserted into com cell genome. ....
You have isolated a DNA fragment containing a human gene involved in lung cancer and are working inserting it into a standard plasmid vector used in molecular cloning which has a multiple cloning site in the lacZ gene. After cutting the DNA fragment and the vector with the same restriction enzyme and ligating the cut DNA, you transform bacteria with hopefully the recombinant vector. How do you expect to identify bacteria with the recombinant vector? A. Bacteria with the recombinant...
You insert a gene for tetracycline resistance into one plasmid and a gene for ampicillin resistance into another plasmid. You successfully introduce both plasmids into a sample of E. coli cells, but fail to grow any of them in culture medium with both antibiotics present in it. What could best explain the problem? A. Random mutation has inactivated the antibiotic resistance genes B. Plasmid incompatibility will not allow both plasmids to persist C. E. coli cannot maintain two plasmids D....
Please answer these four questions.
6C. A type of plasmid used frequently as a vector in recombinant DNA procedures carries gene markers for resistance to tetracycline (Tet') and to ampicillin (Amp). In one experiment, such plasmids were exposed to a restriction enzyme that cuts within the Amp' gene but leaves the Tet' gene intact. Plasmids exposed to the enzyme were next mixed with genomic restriction fragments from a cloned library of mouse DNA. The aim was to produce and detect...
LAB17 Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to the antibiotic ampicillin into a bacterial cell? Objectives After completing this lab, the student will be able to: 1. Demonstrate micropipetting and sterile pipetting techniques for handling and transferring bacteria and plasmid DNA. 2. Maintain sterile conditions for culturing bacterial cells. 3. Inoculate bacteria into flasks, culture tubes, or agar plates. 4. Culture isolated individual colonies from an agar plate to form genetically identical...
You want to use PGLO to produce red fluorescent protein (RFP) instead of green fluorescent protein (GFP). To do so you cut out the GFP gene from PGLO with two restriction enzymes, and replace it with the coding sequence for REP After you successfully created a modified version of the PGLO plasmid with the RFP in place of the GFP you transform this plasmid into E. coli and plate it onto LB plates containing both ampicillin and arabinose. After an...
LAB Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to the antibiotic ampicillin into a bacterial cell? Objectives After completing this lab, the student will be able to: 1. Demonstrate micropipetting and sterile pipetting techniques for handling and transferring bacteria and plasmid DNA. 2. Maintain sterile conditions for culturing bacterial cells. 3. Inoculate bacteria into flasks, culture tubes, or agar plates. 4. Culture isolated individual colonies from an agar plate to form genetically identical...