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Mekanismer for brun- og hvidmuld svampes nedbrydning af tr - Nature

Mekanismer for brun- og hvidmuld svampes nedbrydning af tr - Nature

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Fig. 31.<br />

Vens<strong>tr</strong>e: Vera<strong>tr</strong>yl alkohol (3,4-dimethoxy benzyl alcohol)<br />

Højre: dimethylphenylenediamine<br />

En <strong>tr</strong>edje vigtig gruppe subs<strong>tr</strong>ater <s<strong>tr</strong>ong>for</s<strong>tr</strong>ong> LiP er lignin model <s<strong>tr</strong>ong>for</s<strong>tr</strong>ong>bindelser<br />

bestående <s<strong>tr</strong>ong>af</s<strong>tr</strong>ong> monolignol dimerer (fig. 32), som benyttes til at undersøge ned-<br />

brydningsveje <s<strong>tr</strong>ong>for</s<strong>tr</strong>ong> lignin polymeren.<br />

Fig. 32.<br />

Lignin model <s<strong>tr</strong>ong>for</s<strong>tr</strong>ong>bindelser.<br />

Vens<strong>tr</strong>e: β-1 lignin model.<br />

1-(3,4-diethoxyphenyl-1,3-dihydroxy(4-methoxy-phenyl)-propan.<br />

Højre: β-O-4 model.<br />

1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-1,3-dihydroxypropan<br />

VA har et redox potentiale på 1,36 V <s<strong>tr</strong>ong>og</s<strong>tr</strong>ong> kan oxideres både via LiP-I <s<strong>tr</strong>ong>og</s<strong>tr</strong>ong> LiP-II<br />

med dannelse <s<strong>tr</strong>ong>af</s<strong>tr</strong>ong> radikal kation som følge. Denne omarrangeres via deproton-<br />

ering <s<strong>tr</strong>ong>af</s<strong>tr</strong>ong> C α til en aldehyd (fig. 33) [Baciocchi E. et al. (2002)].<br />

Fig. 33.<br />

Oxidation <s<strong>tr</strong>ong>af</s<strong>tr</strong>ong> vera<strong>tr</strong>yl alkohol til vera<strong>tr</strong>yl aldehyd via deprotonering <s<strong>tr</strong>ong>af</s<strong>tr</strong>ong> C α . [Baciocchi E. et al.<br />

(2002)].<br />

Lignin model <s<strong>tr</strong>ong>for</s<strong>tr</strong>ong>bindelserne oxideres ligesom VA ved dannelse <s<strong>tr</strong>ong>af</s<strong>tr</strong>ong> radikal ka-<br />

Side 49

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