Yamaguchi Yasuhiro, Manita Daisuke, Takeuchi Toshifumi, Kuramochi Kouji, Kuriyama Isoko, Sugawara Fumio, Yoshida Hiromi, Mizushina Yoshiyuki
Department of Applied Biological Science, Tokyo University of Science, Noda, Chiba, Japan.
Biosci Biotechnol Biochem. 2010;74(4):793-801. doi: 10.1271/bbb.90843. Epub 2010 Apr 7.
Trichoderonic acids A (1) and B (2), novel terpenoids, and (+)-heptelidic acid (3) isolated from cultures of a fungus, Trichoderma virens, and their structures were identified by spectroscopic analysis. These compounds selectively and competitively inhibited the activities of mammalian DNA polymerases beta, lambda (pols beta, lambda), and terminal deoxynucleotidyl transferase (TdT) in family X of pols, and compound 2 was a stronger inhibitor than compound 1 or 3. On the other hand, compounds 1-3 did not influence the activities of the other families (A-, B-, and the Y-families) of the mammalian pols tested, and showed no effect on the activities of plant pol alpha, fish pol delta, prokaryotic pol, or the other DNA metabolic enzymes tested. Compound 2 suppressed the growth of two human cancer cell lines, cervix carcinoma cells (HeLa) and breast carcinoma cells (MCF-7). The results suggest that these compounds identified inhibition among the families of mammalian pols.
从真菌绿色木霉的培养物中分离出新型萜类化合物曲霉菌酸A(1)和B(2)以及(+)-庚二酸(3),并通过光谱分析鉴定了它们的结构。这些化合物选择性地、竞争性地抑制了X家族中哺乳动物DNA聚合酶β、λ(聚合酶β、λ)和末端脱氧核苷酸转移酶(TdT)的活性,化合物2是比化合物1或3更强的抑制剂。另一方面,化合物1-3不影响所测试的哺乳动物聚合酶的其他家族(A、B和Y家族)的活性,并且对植物聚合酶α、鱼类聚合酶δ、原核聚合酶或所测试的其他DNA代谢酶的活性没有影响。化合物2抑制了两种人类癌细胞系,子宫颈癌细胞(HeLa)和乳腺癌细胞(MCF-7)的生长。结果表明,这些化合物在哺乳动物聚合酶家族中具有抑制作用。