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Catalyzed by the condensation domain C* (CesA_C2), a second L- O -Val-L-Val-D- O -Leu-D-Ala- S -PCP, produced as described above, is then connected to the TE-bound tetradepsipeptide by esterification, thus forming the octadepsipeptidyl- O -TE intermediate ( DP8 ) and, further on, the dodecadepsipeptide- O -TE ( DP12 ) upon extension by a third L- O -Val-L-Val-D- O -Leu-D-Ala unit prior to macrolactonization to the cyclic twelve residue product cereulide (Fig

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The optimal preparation conditions for FA-CMC-GNA NPs were determined using RSM, with an average particle size of 194.25 nm and a zeta potential of 10.1 mV (Fig

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Intriguingly, some glucose-lowering agents may produce anti-inflammatory actions independent of changes in glucose control