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A recent notable development in relation to the control of GGP and ascorbate synthesis by light is the role of a physical interaction between GGP and a PAS-LOV (PLP) protein
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To facilitate the use of recombinant enzymes to test the substrate specificity in vitro , protein arginine N-methyltransferase (PRMT) was cloned in frame into pGEX vectors using standard molecular biology techniques
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