M back!

ALright. THere is no time for me to dilly dally.

PArt 1: Big Thanks
I returned from my Chiang Mai REcce trip on Tues Night at around midnight so I am still trying to sort out my table from the Teachers' Day bounty because I left in such a rush on that day itself and not forgetting work that lay astrewn. Many thanks for the warm wishes (card, sms, emails etc) and prezzies which I either ate/havent try or havent read. I was expecting the students to be mugging feverishly at home so I didnt think that pple will drop a note which is cool by me. But then those that did, it was nice.

Part 2: Landed and Back to Reality

I have just scanned and posted a revision exercise prepared by Mr Loo which you can try on your own. It is a pdf document and answers are attached. you will be able to find it on R.connect. It is a warm-up exercise for the core paper. (not a mock yah)
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Qn 1: How does Ti plasmid infect the plant cells.

In cloning, there are two ways to go about doing it:
a) after inserting of gene of interest, you perform electroporation so that the plasmid will enter the protoplast. The T-DNA will take care of itself and integrate.
b) after........, you introduce the plasmid back to the bacteria and let the bacteria infect the plant cells/protoplast.

This is to clarify as kindly pointed out by a reader (hahah) - and I have made the appropriate corrections.
For electroporation, we use protoplast culture.
But if you are using Agrobacterium tumefaciens(and yes, there is an 's'), you can either infect a protoplast culture with the bacteria (co-cultivation) or you could inject them into a wounded tissue of the plant and subsequently extract and culture the transformed plant cells.

And I have checked, there is greater efficiency when you use the bacteria instead of electroporation (which is understandable since it is a natural process) =)



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Part 3: Papers

If you are still ultra blur, you might not realised that the sequence of papers is:
Paper 3: application
paper 2: core
paper 1: Mcqs

I leave you to check the dates but apparently, I encountered students who did not realise that.


Application Syllabus: (pls check the details if you need to)
- DNA Cloning (Genetic Engineering)
- DNA Analysis and Genomics
- Human genome project
- Stem cells
- The treatment of genetic diseases in human
- Gene therapy
- Cloning
- Genetic engineering and genetically modified organisms (GMOs)

1 comments:

Anonymous said...

hi if im not wrong, it is hard for plant cells to uptake plasmids thru electroporation cause of the plant cell wall. you mean protoplasts?

I remember reading that the way to do it (i.e grow recombinant plants using tumefaciens) is by introducing the gene of interest into the bacteria, and incubating the bacteria with protoplasts of the plant.then you grow the plant using plant tissue culkture

care to clarify? thanksewz mr chan roxors yay yay wow wow woof meow.

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