Blue-white screening: colourless colonies carry the insert
"Blue-white screening: colourless colonies carry the insert" is a free, interactive Class 12 Biology simulation for NEET, built on the NCERT section "Cloning vectors" in Biotechnology: Principles and Processes. Insert into lacZ (β-galactosidase): with a chromogenic substrate, intact-gene colonies go blue and recombinants stay colourless. NEET has asked about this idea 2 times in 10 years of papers.
From the lesson Cloning vectors in Biotechnology: Principles and Processes. Change the values and watch what happens.
What it shows
NCERT §9.2.2 (i)-(iii)
Insert into lacZ (β-galactosidase): with a chromogenic substrate, intact-gene colonies go blue and recombinants stay colourless.
Controls
3 to try
- Sliderinsert:vector ratio in ligation (illustrative)
- Togglechromogenic substrate on/off
- Tappick a colony to sequence
Try this
Pick a colony that is guaranteed to carry the insert (a colourless one) on the first try.
Common mistake
Reading blue colonies as recombinants.
In NEET
10 years of papers
Asked 2 times in 10 years of NEET.
See the past questions: Cloning Vectors, Biotechnology: Principles and Processes (chapter)
The idea behind it
NCERT §9.2.2 (i)-(iii)
- Plasmids and bacteriophages replicate inside bacterial cells independently of the chromosomal DNA. Phages have very high copy numbers; some plasmids have one or two copies per cell and others 15-100, sometimes more.
- DNA linked to a plasmid or phage is multiplied to that vector's copy number. Modern vectors are engineered to make linking foreign DNA and selecting recombinants easy.
- Origin of replication (ori): the sequence where replication starts. Any DNA linked to it can replicate in the host, and ori also controls the copy number, so a high-copy ori is used to recover many copies.
- Selectable marker: it identifies and eliminates non-transformants and lets transformants grow. Genes for resistance to ampicillin, chloramphenicol, tetracycline or kanamycin are useful markers for E. coli, since normal E. coli resists none of these.
- Cloning sites: the vector should have very few, preferably single, recognition sites for the common restriction enzymes. Several sites would cut it into many fragments and complicate cloning.
- pBR322, an E. coli vector, carries ori, ampR and tetR, rop (which codes for proteins involved in plasmid replication), and sites for Hind III, EcoR I, BamH I, Sal I, Pvu II, Pst I and Cla I.
- Foreign DNA ligated at the BamH I site inside tetR makes the recombinant lose tetracycline resistance. On ampicillin all transformants grow. Moved to tetracycline, recombinants fail while non-recombinants grow on both antibiotics.
- One resistance gene thus selects transformants, while the other, inactivated by the insert, picks out recombinants. Needing two plates makes this cumbersome.
- Easier: insert the DNA into the coding sequence of the enzyme β-galactosidase (insertional inactivation). With a chromogenic substrate, colonies without an insert turn blue; recombinant colonies stay colourless.
Questions
4 answers
- What does the "Blue-white screening: colourless colonies carry the insert" simulation show?
- Insert into lacZ (β-galactosidase): with a chromogenic substrate, intact-gene colonies go blue and recombinants stay colourless.
- What mistake does the "Blue-white screening: colourless colonies carry the insert" simulation fix?
- A common mistake it clears up: reading blue colonies as recombinants.
- Has NEET asked about this idea?
- Yes. NEET has asked about this idea 2 times in 10 years of papers.
- Is this simulation free?
- Yes. It is free and runs in the browser on a phone or a laptop. It belongs to the lesson "Cloning vectors" in Biotechnology: Principles and Processes (Class 12 Biology).
Embed this simulation
Free, with a link back
Teaching this idea? Put the simulation on your own page or LMS with this code.