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156    Advances in textile biotechnology


              for ramie (Boehmeria nivea) raises the possibility of introducing desirable

              traits into another fibre plant (Wang et al., 2009b).
                Another powerful way of introducing genes into plants is the particle
              bombardment method in which metal particles (usually gold or tungsten)
              are coated with multiple copies of the desired gene and introduced directly
              into tissues or cells via a special apparatus (gene gun) (Christou et al., 1988;
              Klein  et al., 1987; Sanford, 1990; Twyman and Christou, 2004). The main
              interest of this method is that it can be used to engineer economically
              important species (maize, rice, sugarcane, wheat, sorghum, papaya, spruce)
              that are currently recalcitrant to transformation by Agrobacterium. More
              recently (Naqvi  et al., 2009), attention has been focused on introducing
              several genes (multigene transfer, MGT) in order to engineer complete
              metabolic pathways. Such an approach is interesting since single-gene trans-
              fer is often unable to modify the physiological pathway targeted.


              7.4    Some examples of engineering in fi bre species

              7.4.1 Cotton

              As indicated above, the most widely cultivated fibre plant is cotton
              (Gossypium hirsutum L.) (Chen et al., 2007; Singh et al., 2009). Cotton fi bres
              are single, long (30–40 mm), epidermal cells of the seed coat that undergo
              synchronous elongation during maturation (Li et al., 2002). The elongating

              fibre is highly vacuolated and its maturation is associated with secondary
              cell wall formation and intensive cellulose biosynthesis, followed by dehy-

              dration and mineral accumulation.  The mature fibre consists mainly of
              cellulose (85–90%) with the rest being composed of hemicelluloses and
              pectins (4–6%), waxes and fats (0.5–1%) and proteins (0–1.5%). Cotton

              fibres contain no, or extremely low amounts of, lignin and other polyphe-
              nolic materials thereby explaining their white coloration (Ioelovich and

              Leykin, 2008). The chemical composition of these fibres, together with their
              form, as well as their relative accessibility post-harvesting, all explain the
              predominant position of cotton in the textile industry.
                Engineering has previously been used to increase the resistance of cotton
              plants to insect attack (Mendelsohn  et al., 2003) and herbicides (Yasuor

              et al., 2006). More recently, a specific ‘cell-wall’-related gene has also been
              targeted (Wang  et al., 2009a). In this study, the down-regulation of the
              GhADF1 gene that codes for an actin depolymerising factor was shown to

              improve cotton fibre properties. This study indicated that the length and

              strength of the transgenic fibres were higher (5.6 and 2–12%, respectively)
              when compared with wild-type fibres. The secondary cell walls of modifi ed


              cotton fibres were also thicker and the deposition of cellulose was increased
              by 3–5% compared with control fibres. Actin is a cellular protein that makes


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