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ý.,,: V. ý ýý . - Nottingham eTheses - University of Nottingham

ý.,,: V. ý ýý . - Nottingham eTheses - University of Nottingham

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Russell, 1984). The most important low temperature active thermo-regulation enzyme in<br />

this pathway is ß-ketoacyl-ACP synthetase II, which elongates palmitoleate to cis-<br />

vaccenate. As the temperature falls, more carbon flows down the unsaturated arm relative<br />

to the saturated arm <strong>of</strong> the split pathway (Russell & Hamamoto, 1998). This increases<br />

unsaturated fatty acids and consequently diunsaturated phospholipids, causing the<br />

transition temperature <strong>of</strong> the membrane to fall (de Mendoza & Cronan, 1983). The<br />

pathway divergence occurs within seconds <strong>of</strong> any temperature reduction. However, once<br />

fatty acid synthetase products have been produced, they must be incorporated into the<br />

membrane lipids and this takes much longer (due to cellular growth and membrane<br />

formation) (Russell & Hamamoto, 1998).<br />

Desaturases (aerobic pathway) can introduce double bonds into fatty acids much<br />

faster than the anaerobic pathway. They have been shown to use intact acyl lipids as their<br />

substrate for double bond insertion in bacteria and algae (Foot et al., 1983). Therefore,<br />

because the fatty acids do not have to be made de novo the system is more rapid. The<br />

desaturase is activated by a decrease in membrane fluidity which is rapidly restored as<br />

exisiting fatty acids are desaturated (Russell & Hamamoto, 1998).<br />

Other mechanisms for transition temperature reduction (i. e. changes in fatty acyl<br />

chain length and the amount or type (anteiso/iso) <strong>of</strong> methyl branching) must be<br />

introduced by the production <strong>of</strong> new fatty acids, because methyl branching is reliant upon<br />

the primer molecule and the chain length is governed by the termination mechanism<br />

(Harwood & Russell, 1984). The mechanism <strong>of</strong> temperature regulation <strong>of</strong><br />

activity/specificity <strong>of</strong> fatty acid synthetase is not well understood (Kaneda, 1991),<br />

however for a review <strong>of</strong> current theories refer to Russell & Hamamoto (1998) and Russell<br />

& Nichols (1999).<br />

1.6 -<br />

Biodiversity and biogeography <strong>of</strong> bacteria<br />

There have been numerous extensive studies on microbial diversity and ecology within<br />

Antarctic ecosystems (Hand, 1980; Hand & Burton, 1981; Wright & Burton, 1981; Burke<br />

& Burton, 1988; Franzmann et al., 1990; Mancuso et al., 1990; Franzmann & Rohde,<br />

1991,1992; Laybourn-Parry & Marchant, 1992b; James et al., 1994. Ellis-Evans, 1985a:<br />

Laybourn-Parry et al., 1996; Laybourn-Parry, 1997; Ellis-Evans et al., 1998; Murray et<br />

al., 1998. Nichols et al., 1999, Bowman et al., 2000a and b; Waters et al., 2000; Brown<br />

20

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