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Surface Modification of Cellulose Acetate with Cutinase and ...

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<strong>Surface</strong> <strong>Modification</strong> <strong>of</strong> <strong>Cellulose</strong> <strong>Acetate</strong> <strong>with</strong> <strong>Cutinase</strong> <strong>and</strong> <strong>Cutinase</strong> Fused to Carbohydrate-binding Modules<br />

Figure 4. DRIFT spectra showing the carbonyl group stretching b<strong>and</strong> <strong>of</strong> (A) CDA <strong>and</strong><br />

(B) CDT controls <strong>and</strong> samples. The samples (2% w/v) were treated <strong>with</strong> 25 U mL -1 <strong>of</strong><br />

cutinase, at pH 8 <strong>and</strong> 30º C, for 24 hours. The controls were treated under the same<br />

conditions but <strong>with</strong>out enzyme.<br />

After the fabric samples <strong>and</strong> controls were competitively stained, cross sections <strong>of</strong><br />

fibres were made <strong>and</strong> observed by Fluorescence microscopy to assess the diffusion <strong>of</strong><br />

the dye inside the fibre <strong>and</strong> indirectly to confirm the surface action <strong>of</strong> cutinase.<br />

The inherent affinity <strong>of</strong> Remazol Reactive Blue R for CDA did not allow any<br />

significant difference in the dye distribution in the fibres (results not showed). The<br />

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