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The synthetase components were purified to homogeneity as shown in Figure S1 (Supporting Information). EntB and EntF were correctly pantotetheinylated as shown by MALDI-ToF spectra in Figures S3 and S4 (Supporting Information). The linear side products and enterobactin were identified by ESI-ToF mass spectrometry as shown in Figure S5 (Supporting Information
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The synthetase components were purified to homogeneity as shown in Figure S1 (Supporting Information). EntB and EntF were correctly pantotetheinylated as shown by MALDI-ToF spectra in Figures S3 and S4 (Supporting Information). The linear side products and enterobactin were identified by ESI-ToF mass spectrometry as shown in Figure S5 (Supporting Information).
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The EntB saturation reported in ref 11 is able to reduce the side products from >80% to 25% at a low EntF concentration, but unable to completely suppress their formation. It actually increases the side product formation physiological EntF concentration. Figure S8 in the Supporting Information for more details. The premature release of linear side products is universally suppressed by 30% Ficoll 70 to < 5% irrespective of the composition of the synthetase
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The EntB saturation reported in ref 11 is able to reduce the side products from >80% to 25% at a low EntF concentration, but unable to completely suppress their formation. It actually increases the side product formation at the physiological EntF concentration. See Figure S8 in the Supporting Information for more details. The premature release of linear side products is universally suppressed by 30% Ficoll 70 to < 5% irrespective of the composition of the synthetase.
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