Okamoto Susumu, Sakurada Masaru, Kubo Yasuyuki, Tsuji Gento, Fujii Isao, Ebizuka Yutaka, Ono Makoto, Nagasawa Hiromichi, Sakuda Shohei
Department of Applied Biological Chemistry, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan1.
Faculty of Agriculture, Kyoto Prefectural University, Shimogamo, Kyoto 606-8522, Japan2.
Microbiology (Reading). 2001 Sep;147(Pt 9):2623-2628. doi: 10.1099/00221287-147-9-2623.
The effect of aflastatin A (AsA), a novel inhibitor of aflatoxin production, on melanin biosynthesis of Colletotrichum lagenarium was examined. Addition of a low concentration of AsA (0.5 microg ml(-1)) to the culture medium almost completely inhibited the melanin production of this organism. AsA also inhibited the production of scytalone, an early intermediate of melanin biosynthesis. Melanin production was restored by addition of exogenous scytalone in the presence of AsA, suggesting that the late steps after the synthesis of scytalone were not significantly affected by AsA. This was confirmed by the results from RT-PCR analysis of the expression of genes encoding melanin biosynthetic enzymes (SCD1, THR1) and a regulatory gene (CMR1). By contrast, expression of PKS1 was severely impaired by AsA, although catalytic activity of a polyketide synthase (PKS1) was not inhibited by AsA. These results indicate that AsA inhibits an early step in melanin production, which suppresses the expression of PKS1.
研究了新型黄曲霉毒素产生抑制剂阿弗他汀A(AsA)对葫芦科炭疽菌黑色素生物合成的影响。向培养基中添加低浓度的AsA(0.5微克/毫升)几乎完全抑制了该生物体的黑色素产生。AsA还抑制了黑色素生物合成的早期中间体scytalone的产生。在AsA存在的情况下,通过添加外源性scytalone可恢复黑色素的产生,这表明scytalone合成后的后期步骤未受到AsA的显著影响。黑色素生物合成酶(SCD1、THR1)和调控基因(CMR1)编码基因表达的RT-PCR分析结果证实了这一点。相比之下,尽管聚酮合酶(PKS1)的催化活性未被AsA抑制,但AsA严重损害了PKS1的表达。这些结果表明,AsA抑制黑色素产生的早期步骤,从而抑制PKS1的表达。