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We are not aware of current pharmacological approaches which can selectively inhibit the pathogenic aspects of inflammation without potentially interfering with the benefits of phagocyte recruitment and activation

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As the identified di-, hexa- and decadepsipeptides are not in line with the proposed biosynthetic assembly of three ready-made tetradepsipeptides 8,9 , these findings prompted us to ask whether the candidate depsipeptide esters are released from chemically unstable NRPS-bound PCP- S -ester or TE- O -ester intermediates of cereulide biosynthesis upon transesterification with ethanol, or are formed as artifacts by esterification of free depsipeptides or as cereulide degradation products released upon ethanolysis

The promoter regions were recombined using Gateway technology into the binary vector pBGYN