Polyketide synthase genes in insect- and nematode-associated fungi

被引:39
作者
Lee, T
Yun, SH
Hodge, KT
Humber, RA
Krasnoff, SB
Turgeon, GB
Yoder, OC
Gibson, DM
机构
[1] ARS, USDA, NAA, US Plant Soil & Nutr Lab, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Plant Pathol, Ithaca, NY 14853 USA
关键词
D O I
10.1007/s002530100637
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Production of polyketides is accomplished through complex enzymes known as polyketide synthases (PKS); these enzymes have highly conserved domains that might be useful in screens for PKSs in diverse groups of organisms. A degenerate PCR-based approach was used to amplify PKS fragments of the ketosynthase domain from genomic DNA of a group of insect- and nematode-associated fungi. Of 157 isolates (representing 73 genera and 144 species) screened, 92 isolates generated PCR products of predicted size (similar to 300 bp). The ability to detect PKS domains was a function of the number of different primer pairs employed in the screen. Cloning and sequencing revealed that 66 isolates had at least one unique PKS sequence; ten members of this set contained multiple PKS fragments, for a total of 76 unique PKS fragments. Since PKS genes appear to be widespread among fungi, a PCR-based screening system appears to be an efficient, directed means to identify organisms having the potential to produce polyketides.
引用
收藏
页码:181 / 187
页数:7
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