err they all seem pretty correct to me 
Any particular reason you think D is wrong???
I'll ask the lecturer.
It's a tough question that's for sure. These are my thoughts:
I think A is good because that describes protein recognition, one of the suggested approaches.
I'm tossing up between B and C as the approaches you would not use.
I think D is correct because it describes using functional complementation and the approach looks like it is being done properly, i.e. isolating the his auxotrophs which have now been turned into a his prototrophs.
The reason I thought B was because it says a "degenerate oligonucleotide", however in the lectures we have been told that the olignonucleotide probe should be designed from the least degenerate region of the mrna sequence.
The reason I thought C might be incorrect is because I think the library should be made from the His6 wild-type strain.
So would you say B or C? :S I'm leaning towards C
q34 from 2008 has a similar question