Tsuji Gento, Sugahara Tomomi, Fujii Isáo, Mori Yuichiro, Ebizuka Yutaka, Shiraishi Tomonori, Kubo Yasuyuki
Laboratory of Plant Pathology, Graduate School of Agriculture, Kyoto Prefectural University, Kyoto 606-8522, Japan.
Mycol Res. 2003 Jul;107(Pt 7):854-60. doi: 10.1017/s0953756203008001.
Colletotrichum lagenarium is a plant pathogenic fungus, and produces melanin that is an essential factor for appressorial penetration into host tissues. The melanin biosynthesis pathway of C. lagenarium starts with pentaketide synthesis catalyzed by polyketide synthase Pks1p. We previously confirmed that the direct product of Pks1p is 1,3,6,8-tetrahydroxynaphthalene. Thus, melanin biosynthesis in this fungus requires the reduction of 1,3,6,8-tetrahydroxynaphthalene to scytalone. We made a double mutant 9141-144 from the thr1 mutant 9141 that lacks the ability to metabolize 1,3,8-trihydroxynaphthalene. The double mutant 9141-144 could metabolize neither 1,3,6,8-tetrahydroxynaphthalene nor 1,3,8-trihydroxynaphthalene. However melanin production by the double mutant was restored by THR1, indicating that Thr1p can metabolize both compounds in vivo. These results demonstrate that two enzymes, Thr1p and a deduced 1,3,6,8-tetrahydroxynaphthalene-specific reductase, are involved in the first reduction step of the melanin biosynthesis pathway of C. lagenarium.
葫芦炭疽菌是一种植物病原真菌,可产生黑色素,而黑色素是附着胞穿透宿主组织的关键因素。葫芦炭疽菌的黑色素生物合成途径始于由聚酮合酶Pks1p催化的五酮合成。我们之前证实Pks1p的直接产物是1,3,6,8-四羟基萘。因此,该真菌中的黑色素生物合成需要将1,3,6,8-四羟基萘还原为鬼臼毒素。我们从缺乏代谢1,3,8-三羟基萘能力的thr1突变体9141中构建了双突变体9141-144。双突变体9141-144既不能代谢1,3,6,8-四羟基萘也不能代谢1,3,8-三羟基萘。然而,THR1恢复了双突变体的黑色素生成,这表明Thr1p可以在体内代谢这两种化合物。这些结果表明,两种酶,即Thr1p和一种推测的1,3,6,8-四羟基萘特异性还原酶,参与了葫芦炭疽菌黑色素生物合成途径的第一步还原反应。