Comment Why all at once? (Score 1) 30
I assume that, as an exercise, getting 5 simultaneous introductions working makes for a better paper; but is there a reason why you would want that in practice? Especially if there is any wobble in the ratios either randomly, across generations, or in the presence of certain environmental conditions that tweak the plant's metabolism one way or another that sounds like it would be a real pain in the ass to have to re-balance (and, if different patients are deemed to need different combinations even a perfectly stable plant is going to need re-balancing of the outputs) vs. very specifically going for a specific target output per-plant(or e. coli or yeast or whatever is easiest to bioreactor) and then just mixing to taste after purification. Is there some advantage I'm not seeing?
I realize that there are cases where some plant-sourced pharmacological effect looks like it is actually driven not by the identified 'active ingredient'; but by dozens or hundreds of assorted things, and in that case you just have to live with the complexity if you get better results with that than with purified isolates; but if you are deliberately engineering for very specific outputs why a mix of 5?
I realize that there are cases where some plant-sourced pharmacological effect looks like it is actually driven not by the identified 'active ingredient'; but by dozens or hundreds of assorted things, and in that case you just have to live with the complexity if you get better results with that than with purified isolates; but if you are deliberately engineering for very specific outputs why a mix of 5?