DOI QR코드

DOI QR Code

Analysis of the MAT1-1 and MAT1-2 Gene Ratio in Black Koji Molds Isolated from Meju

  • Mageswari, Anbazhagan (Korean Agricultural Culture Collection, Agricultural Microbiology Division, National Institute of Agricultural Science) ;
  • Kim, Jeong-seon (Korean Agricultural Culture Collection, Agricultural Microbiology Division, National Institute of Agricultural Science) ;
  • Cheon, Kyu-Ho (Korean Agricultural Culture Collection, Agricultural Microbiology Division, National Institute of Agricultural Science) ;
  • Kwon, Soon-Wo (Korean Agricultural Culture Collection, Agricultural Microbiology Division, National Institute of Agricultural Science) ;
  • Yamada, Osamu (National Research Institute of Brewing) ;
  • Hong, Seung-Beom (Korean Agricultural Culture Collection, Agricultural Microbiology Division, National Institute of Agricultural Science)
  • 투고 : 2016.10.31
  • 심사 : 2016.11.16
  • 발행 : 2016.12.30

초록

Aspergillus luchuensis is known as an industrially important fungal species used for making fermented foods such as awamori and shochu in Japan, makgeolli and Meju in Korea, and Pu-erh tea in China. Nonetheless, this species has not yet been widely studied regarding mating-type genes. In this study, we examined the MAT1-1 and MAT1-2 gene ratio in black koji molds (A. luchuensis, Aspergillus niger, and Aspergillus tubingensis) and in Aspergillus welwitschiae isolated from Meju, a fermented soybean starting material for traditional soy sauce and soybean paste in Korea. The number of strains with the MAT1-1 locus was 2 of 23 (A. luchuensis), 6 of 13 (A. tubingensis), 21 of 28 (A. niger), and 5 of 10 (A. welwitschiae). Fungal species A. tubingensis and A. welwitschiae showed a 1 : 1 ratio of MAT1-1 and MAT1-2 mating-type loci. In contrast, A. luchuensis revealed predominance of MAT1-2 (91.3%) and A. niger of MAT1-1 (75%). We isolated and identified 2 A. luchuensis MAT1-1 strains from Meju, although all strains for making shochu in Japan are of the MAT1-2 type. These strains may be a good resource for breeding of A. luchuensis to be used in the Asian fermented-food industry.

키워드

참고문헌

  1. Hong SB, Yamada O, Samson RA. Taxonomic re-evaluation of black koji molds. Appl Microbiol Biotechnol 2014;98:555-61. https://doi.org/10.1007/s00253-013-5332-9
  2. Hong SB, Lee M, Kim DH, Varga J, Frisvad JC, Perrone G, Gomi K, Yamada O, Machida M, Houbraken J, et al. Aspergillus luchuensis, an industrially important black Aspergillus in East Asia. PLoS One 2013;8:e63769. https://doi.org/10.1371/journal.pone.0063769
  3. Inui T. Ryukyu awamori hakko kin chyosa houkokusyo. J Tokyo Chem Soc 1901;22:669-88.
  4. Hong SB, Kim DH, Kim SH, Bang N, Kwon SW. Identification of black Aspergillus strains isolated from Meju. Kor J Mycol 2013;41:132-5. https://doi.org/10.4489/KJM.2013.41.2.132
  5. Hong SB, Kim DH, Samson RA. Aspergillus associated with Meju, a fermented soybean starting material for traditional soy sauce and soybean paste in Korea. Mycobiology 2015;43:218-24. https://doi.org/10.5941/MYCO.2015.43.3.218
  6. Glass NL, Vollmer SJ, Staben C, Grotelueschen J, Metzenberg RL, Yanofsky C. DNAs of the two mating-type alleles of Neurospora crassa are highly dissimilar. Science 1988;241:570-3. https://doi.org/10.1126/science.2840740
  7. Debuchy R, Berteaux-Lecellier V, Silar P. Mating systems and sexual morphogenesis in ascomycetes. In: Borkovich KA, Ebbole DJ, editors. Cellular and molecular biology of filamentous fungi. Washington, DC: American Society for Microbiology; 2010. p. 501-35.
  8. Dyer PS. Sexual reproduction and significance of MAT in the aspergilli. In: Heitman J, Kronstad JW, Taylor JW, Casselton LA, editors. Sex in fungi: molecular determination and evolutionary implications. Washington, DC: ASM Press; 2007. p. 123-42.
  9. Paoletti M, Seymour FA, Alcocer MJ, Kaur N, Calvo AM, Archer DB, Dyer PS. Mating type and the genetic basis of self-fertility in the model fungus Aspergillus nidulans. Curr Biol 2007;17:1384-9. https://doi.org/10.1016/j.cub.2007.07.012
  10. Rydholm C, Dyer PS, Lutzoni F. DNA sequence characterization and molecular evolution of MAT1 and MAT2 mating-type loci of the self-compatible ascomycete mold Neosartorya fischeri. Eukaryot Cell 2007;6:868-74. https://doi.org/10.1128/EC.00319-06
  11. Ramirez-Prado JH, Moore GG, Horn BW, Carbone I. Characterization and population analysis of the mating-type genes in Aspergillus flavus and Aspergillus parasiticus. Fungal Genet Biol 2008;45:1292-9. https://doi.org/10.1016/j.fgb.2008.06.007
  12. Szewczyk E, Krappmann S. Conserved regulators of mating are essential for Aspergillus fumigatus cleistothecium formation. Eukaryot Cell 2010;9:774-83. https://doi.org/10.1128/EC.00375-09
  13. Debuchy R, Turgeon BG. Mating-type structure, evolution, and function in Euascomycetes. In: Kues U, Fischer R, editors. The Mycota, Vol. I. Growth, differentiation and sexuality. Berlin: Springer-Verlag; 2006. p. 293-323.
  14. Singh G, Dyer PS, Ashby AM. Intra-specific and inter-specific conservation of mating-type genes from the discomycete plant-pathogenic fungi Pyrenopeziza brassicae and Tapesia yallundae. Curr Genet 1999;36:290-300. https://doi.org/10.1007/s002940050503
  15. Paoletti M, Rydholm C, Schwier EU, Anderson MJ, Szakacs G, Lutzoni F, Debeaupuis JP, Latge JP, Denning DW, Dyer PS. Evidence for sexuality in the opportunistic fungal pathogen Aspergillus fumigatus. Curr Biol 2005;15:1242-8. https://doi.org/10.1016/j.cub.2005.05.045
  16. Archer DB, Dyer PS. From genomics to post-genomics in Aspergillus. Curr Opin Microbiol 2004;7:499-504. https://doi.org/10.1016/j.mib.2004.08.003
  17. Galagan JE, Calvo SE, Cuomo C, Ma LJ, Wortman JR, Batzoglou S, Lee SI, Basturkmen M, Spevak CC, Clutterbuck J, et al. Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature 2005;438:1105-15. https://doi.org/10.1038/nature04341
  18. Pel HJ, de Winde JH, Archer DB, Dyer PS, Hofmann G, Schaap PJ, Turner G, de Vries RP, Albang R, Albermann K, et al. Genome sequencing and analysis of the versatile cell factory Aspergillus niger CBS 513.88. Nat Biotechnol 2007;25:221-31. https://doi.org/10.1038/nbt1282
  19. Wada R, Maruyama J, Yamaguchi H, Yamamoto N, Wagu Y, Paoletti M, Archer DB, Dyer PS, Kitamoto K. Presence and functionality of mating type genes in the supposedly asexual filamentous fungus Aspergillus oryzae. Appl Environ Microbiol 2012;78:2819-29. https://doi.org/10.1128/AEM.07034-11
  20. O'Gorman CM, Fuller H, Dyer PS. Discovery of a sexual cycle in the opportunistic fungal pathogen Aspergillus fumigatus. Nature 2009;457:471-4. https://doi.org/10.1038/nature07528
  21. Varga J, Szigeti G, Baranyi N, Kocsube S, O'Gorman CM, Dyer PS. Aspergillus: sex and recombination. Mycopathologia 2014;178:349-62. https://doi.org/10.1007/s11046-014-9795-8
  22. Horn BW, Olarte RA, Peterson SW, Carbone I. Sexual reproduction in Aspergillus tubingensis from section Nigri. Mycologia 2013;105:1153-63. https://doi.org/10.3852/13-101
  23. Yamada O, Machida M, Hosoyama A, Goto M, Takahashi T, Futagami T, Yamagata Y, Takeuchi M, Kobayashi T, Koike H, et al. Genome sequence of Aspergillus luchuensis NBRC 4314. DNA Res 2016 Sep 20 [Epub]. https://doi.org/10.1093/dnares/dsw032.
  24. Kothe E. Mating-type genes for basidiomycete strain improvement in mushroom farming. Appl Microbiol Biotechnol 2001;56:602-12. https://doi.org/10.1007/s002530100763
  25. Bohm J, Hoff B, O'Gorman CM, Wolfers S, Klix V, Binger D, Zadra I, Kurnsteiner H, Poggeler S, Dyer PS, et al. Sexual reproduction and mating-type-mediated strain development in the penicillin-producing fungus Penicillium chrysogenum. Proc Natl Acad Sci U S A 2013;110:1476-81. https://doi.org/10.1073/pnas.1217943110
  26. Poggeler S. Mating-type genes for classical strain improvements of ascomycetes. Appl Microbiol Biotechnol 2001;56:589-601. https://doi.org/10.1007/s002530100721