Optimization of Culture Media and ITS Identification of Tricholoma matsutake

Article Preview

Abstract:

Aims: To optimize the culture media of 0288 Tricholoma matsutake and to identify it according to its rDNA ITS sequence. Methods: Fruit body, collected from Heilongjiang province, is used as the material, and the mycelium is isolated and radiated under ultraviolet. Then the radiated mycelium is cultured in five different media and its morphology of fungus colony and growth rate are investigated. After that, the rDNA ITS sequences of 0288 and the natural fruit body of T. matsutake are analyzed and identified by PCR and sequencing. Results: The radiated mycelium grew faster in formula A culture medium than others and its average growth rate is up to 0.575mm/d. Results also showed that the homology of the rDNA ITS sequence is almost up to 99% between 0288 and the natural fruit body. Through this experiment, the best growth condition of 0288 is obtained and its fruit body is induced as pure cultural product. It would lay strong foundation for the artificial domestication of the wild T. matsutake.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 634-638)

Pages:

1574-1580

Citation:

Online since:

January 2013

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Akiyoshi Y, Ken M, Masatake O(1999). Ectomycorrhiza formation of Tricholoma matsutake isolates on seedlings of Pinus densiflora in vitro. Mycoscience, 40: 455-463

DOI: 10.1007/bf02461022

Google Scholar

[2] Chapela I H, Garbelotto M(2004). Phylogeography and evolution in matsutake and close allies inferred by analyses of ITS sequences and AFLPs. Mycologia, 96: 730-741.

DOI: 10.1080/15572536.2005.11832921

Google Scholar

[3] Chen Q, Liao DC, Zhang XP, Zhang CB and Li DY(2003). Preliminary analysis of genetic characteristics of edible fungus Tricholoma matsutake isolated from Yajiang, China, by AFLP Technique. Agricultural Sciences in China, 2(2): 229-236

Google Scholar

[4] Chen Y, Wang FZ, Chen YL, Gong MQ(2000). Studies on Culture Conditions of Tricholoma matsutake. Forest Research, 13(4): 410-415(in Chinese with English abstract)

Google Scholar

[5] Hirokazu K, Keiko H, Ryo T, Nakamura T, Sato Y, Akiyama Y, Sano M and Tanaka O(2004). Growth promotion of mycelia of the matsutake mushroom Tricholoma matsutake by D-Isoleucine. Biosci, Biotechnol, Biochem, 68(11):2405-2407

DOI: 10.1271/bbb.68.2405

Google Scholar

[6] Kikuchi K, Matsushita N, Guerin-Laguette A, Ohta A and Suzuki K(2000). Detection of Tricholoma matsutake by specific ITS primers. Mycol Res, 104 (12): 1427-1430

DOI: 10.1017/s0953756200002653

Google Scholar

[7] Matsushita N, Kikuchi K, Sasaki Y, Guerin-Laguette A, Lapeyrie F, Vaario LM, Intini M and Suzuki K(2005). Genetic relationship of Tricholoma matsutake and T. nauseosum from the northern hemisphere based on analyses of ribosomal DNA spacer regions. Mycoscience, 46: 90-96

DOI: 10.1007/s10267-004-0220-x

Google Scholar

[8] Murata H, Babasaki K, Yamada A(2005). Highly polymorphic DNA markers to specify strains of the ectomycorrhizal basidiomycete Tricholoma matsutake based on σmarY1, the long terminal repeat of gypsy-type retroelement marY1. Mycorrhiza, 15: 179-186.

DOI: 10.1007/s00572-004-0319-0

Google Scholar

[9] Schmidt O, Moreth U(2002). Data bank of rDNA-ITS sequences from building-rot fungi for their identification. Wood Science and Technology, 36: 429-433

DOI: 10.1007/s00226-002-0152-6

Google Scholar

[10] Sha T, Zhang HB, Ding HS, Li ZJ, Cheng LZ, Zhao ZW and Zhang YP(2007). Genetic diversity of Tricholoma matsutake in Yunnan Province. Chinese Science Bulletin. 52(9):1212-1216.

DOI: 10.1007/s11434-007-0194-0

Google Scholar

[11] Thoquet P, Gherardi M, Joumet E P, Kereszt A, Ané JM, Prosperi JM and Huguet T( 2002). The molecular genetic linkage map of the model legume Medicago truncatula: an essential tool for comparative legume genomics and the isolation of agronomically important genes. BMC Plant Biology, 2 (1): 1-13.

DOI: 10.1007/978-3-662-05036-1_14

Google Scholar

[12] Vos P R, Hogers R, Reijans T, Bleeker M, Reijans M, Lee TV, Hornes M, Friters A, Pot J, Paleman J, Kuiper M and Zabeau M( 1997). AFLP: a new technique for DNA fingerprinting. Nuclear Acid Research, 23: 4407-4414.

DOI: 10.1093/nar/23.21.4407

Google Scholar

[13] Wei TZ, Xu GB, Fu WJ, Liang YJ, Liu WL(2007). Effect of different kinds of media on the growth status of Tricholoma matsutake mycelium. Acta Edulis Fungi (3): 48-52(in Chinese with English abstract)

Google Scholar

[14] Wipe D, Munch J, Botton B and Buscot F(1996). DNA polymorphism in morels: complete sequences of the internal transcribed spacer of genes coding for rRNA in Morchella esculenta (Yellow Morel) and Morchella conica (Black Morel). Applied and Environmental Microbiology, 62(9): 3541-3543

DOI: 10.1128/aem.62.9.3541-3543.1996

Google Scholar

[15] Yang MH, Liu YM, Yang XM, Chen LG(1997). Isolation and pure culture studies on Tricholoma matsutake. Journal of Huazhong Agricultural University, 16(3): 16(3): 272-276(in Chinese with English abstract)

Google Scholar

[16] Yamada A, Kobayashi H, Murata H(2003). Tricholoma matsutake IFO6933 and IFO30604, "matsutake" isolates that have been maintained on slants and widely used in vitro for a quarter to half a century, can form ectomycorrhiza in Pinus densiflora. Mycoscience, 44: 249-251

DOI: 10.1007/s10267-003-0098-z

Google Scholar