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178    Advances in textile biotechnology



              washable wool without signifi cant fibre damage (Heine et al., 2000). Recently,
              scanning electron microscopy (SEM) has been used to observe the degrada-

              tion of wool fibre cross-sections caused by proteases digestion. The SEM

              images confirmed that the proteases preferentially digest the cystine-poor
              endocuticle, cell membranes, nuclear remnants, and intermacrofi brillar
              materials on the wool cross-sections (Okada et al., 2008).
                During enzymatic treatment of wool using proteases on their own, an
              early study (Moncrieff, 1953) showed that the attack on wool fi bres is vari-

              able.  The enzymes appear to attack weathered fibres more rapidly and

              therefore attack the tips of fibres more than the root ends. Irregularity of

              damage of fibres by enzymes was clearly shown by SEM.
                Bishop et al. (1998) reported that carefully controlled treatments with
              proteolytic enzymes can reduce the buckling load and collapse energy of
              wool yarns.  These treatments were shown to improve the softness and
              reduce the subjectively perceived prickle of wool fabric knitted from the
              treated yarns. The combination of chlorination and treatments with proteo-
              lytic enzyme was also reported to improve handle properties, especially for

              coarse wool and mohair fibres, as well as improving fibre whiteness, without

              causing any significant damage to the wool (Holme, 2006).

                Enzymatic treatments for lipid removal have been studied to make the
              wool fibre more hydrophilic, in order to make subsequent enzymatic treat-

              ment more efficient.  Triacylglycerol lipase (EC 3.1.1.3) and lipoprotein

              lipase (EC 3.1.1.34) have been used. Heine (Heine, 1991; Nolte et al., 1996)
              investigated the removal of lipids from the outer surface layer of the wool

              fibre by treating grease-free wool with a lipoprotein lipase. It was found
              that the aliphatic hydrocarbon content of the cuticle surface was reduced

              by 20%. Mall  et al. (2002) used ToF-SIMS (time-of-flight secondary ion
              mass spectrometry) surface analysis to monitor the loss of surface lipids
              caused by treatment of scoured wool with lipases. It was found that the
              anionic surfactants left on the surface of wool fibre from the scouring

              process might inhibit the enzyme. No change in the fibre wettability was

              observed, probably because the integrity of the hydrophobic surface layer

              was not sufficiently attacked by the enzymes. Recently, Wang et al. (2010)

              investigated the effect of lipase treatment on the fibre surface of wool
              fabrics cleaned by soxhlet extraction with chloroform/methanol 87 : 13(v/v).
              It was reported that the lipase treatment hardly affects the cuticle surface
              of the wool, resulting in no noticeable improvement of wettability.
                The use of cutinase to hydrolyse the outermost bound lipids in the wool
              surface has recently been investigated. Cutinase has hydrolytic activity
              towards a broad variety of aliphatic esters. Wang et al. (2009) reported that
              treatment by cutinase can improve the wettability of wool fabrics from a
              contact angle of 135° to 92° after 4 h incubation with cutinase activity at
                    −1
              10 U g  fabric. However, cutinase can not achieve the complete removal



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