With two chiral centres, you can form 4 different isomers.
When only one chiral centre is changed at a time, sets of diastereoisomers are formed.
It also means that the sulfur can be a chiral centre.
Still other enzymes produce new chiral centers, always with a high specificity.
Why isn't it possible to orient the groups around the chiral center to achieve more forms?
This is due to the extra chiral center at C-2.
This is a very good way to create new chiral centres.
A meso compound need not even have a chiral center.
This is particularly the case in the synthesis of molecules with chiral centres.
The 2-ketopentoses have two chiral centers, and therefore four different stereoisomers are possible.