Flammulina velutipes belonging to white rot fungi is one of the commercially important edible mushrooms and is produced in large quantities due to the introduction of a automated and mechanized cultivation system in Korea. Despite the chief item of export among edible mushrooms, Flammulina velutipes has the lowest distribution rate of domestic cultivar, estimated that about 20 percent. As the result that most white cultivars of Flammulina velutipes produced and exported in Korea were introduced from Japan, farmers pay a large amount of royalties. Therefore, we try to develop a new pure domestic cultivars as a substitute for Japanese cultivars. To breed both white and gold superior strains, we selected the crossing mother groups including 10 white strains of ASI 4198 etc. and 7 brown strains of ASI 4049 etc. and mated each of the 17 strains by mon-mon hybridization. 19 white and 14 brown strains were chosen through two selection experiment over 2014 2016. In the third selection experiment this year, we finally selected one white(Fv 16 c 37) and the other gold(Fv 15 a 31) strain. Two selected strains were cultivated in the same environmental conditions. Spawn running period on the sawdust substrate required 30days at 20°C. The cultivation period and optimum temperature were 12±1 days at 14°C for primordia formation, 5 days at 4°C for inhibition phase, and 14±1 days at 7°C for fruiting body development. The length of pilei and stipes in two selected strains and Megumi as a control Japanese cultivar harvested in optimal stage was as follows: 10.5±0.81mm and 139.7±4.23mm in Fv 16 c 37, 10.8±0.43mm and 128..2±7.31mm in Fv 15 a 31, and 10.9±0.41mm and 141.8±4.64mm in Megumi respectively. The Yield of Fv 16 c 37, Fv 15 a 31 and Megumi was 271.2±11.84g, 237.7±9.05g and 270.7±16.87g per 1100ml in bottle cultivation.

There are three kinds of Pleurotus eryngii : P. eryngii var. eryngii (P. eryngii), P. eryngii var. ferula (P. ferula : A-Wei-Mo) P. eryngii var. nebrodensis (P. nebrodensis : Bai-Ling-Gu). We bred P. ferula using Di-Mon mating and physiological assay and selected as follow (1) ‘Beesan No.1’ produced high yields, (2) ‘Beesan No.2’ was excellent morphological shape and anti-adipogenic Activit, (3) ‘Ergo’ included high ergothioneine such as anto-oxidant material, (4) ‘GW10-45’ included highest ergothioneine such as anto-oxidant material, (5) ‘Maeksong’ included high ergothioneine and effect of anti-inflammatory. We suggest that there are able to food-medicine materials.

Two strains one of 29 strains were picked out Hm1-1, and Hm3-10 as parental strains for breeding, such as Hm1-1 was taken 15 point as the highest grade. Because Hm3-10 was wild strain collected form Deogyu mountain. The result of RAPD has shown that 29 strains fell into 6 distinct groups while a wild strain collected from DeogYu Mt. did not belong to any of the groups. The 20 selected monokaryon mycelia were crossed by Hm3-10 × Hm1-1, and then we picked up dikaryotic mycelia which did form clamp connection. We acquired 343 dikaryons from Hm3-10 × Hm1-1 with the mating rates of 85.7%, respectively. Total 343 dikaryon strains were cultivated and then 58 strains with good morphological and cultivation characteristics were selected. The differences of the 58 strains were verified by morphology of fruiting bodies. Finally, we selected 3 new strains (Hm15-3, Hm15-4, Hm17-5). Lastly, in order to develop molecular markers that can identify developed 3 new cultivars, were subjected to the random amplified polymorphic DNA (RAPD) analysis using 3 commercially available random primer sets (OPS-1, OPS-10, and OPL-13). I selected 10 distinct DNA bands from the three RAPD gels which were amplified with OPS-1, OPS-10, or OPL-13 primers. Bands 1, 6, and 7 were unique for Hm1-1 and Hm1-6. Bands 2∼5 and 8∼10 were unique for Hm3-10. The sequences were deposited in GeneBank and were used to design the 15-base primer sets using their 5’- and 3’-ends. The primer sets P1∼P5 and P7 produced DNA bands with corresponding sizes from all H. marmoreus strains and presented no strain specificity. The P6 marker appeared only for Hm1-1 while the P8 marker appeared for most hybrid strains except Hm16-1 and the wild Hm3-10. This is interesting because the P6 marker showed broader specificity than the P8 marker in the identification of strains. The P9 marker appeared on Hm16-1, Hm16-2, Hm17-5, and Hm3-10 and the P10 marker appeared on Hm15-3, Hm15-4, Hm16-1, Hm16-2, and Hm3-10. The hybrid strain Hm15-3 was the only strain that did not contain either the P9 or P10 marker. The resulting DNA markers were applied for the identification of the strains and employed for the molecular breeding of H. marmoreus.

1980년도부터 우리나라 Burley 종 잎담배산지에서 엽맥에 녹대병상 또는 괴저증상을 나타내는 새로운 병징이 관찰되기 시작하였다. 기주범위조사, 항혈청반응, 물리적성질조사, 복숭아혹진딧물에 의한 전염여부 및 바이러스 입자 관찰을 통해 이들은 서로 병징을 달리하는 PYY의 두가지 계통으로 밝혀졌다. 이 계통들은 잎담배포장에서 자연감염에 의해 나타난 주요병징에 따라 엽맥연대계통 (PVY-VB)과 엽맥괴저계통 (PVY-VN) 으로 명명하였다. PVY 항혈청과 이 계통들의 이병즙액을 반응시킨 결과 양성반응을 나타냈으며 그 반응에서는 두계통간의 차가 없었다. 이들과 병징이 유사한 tobacco etch virus 및 tobacco vein mottling virus 항혈청과의 반응에서는 음성반응을 나타냈다. 전자현미경에 의해 약 730 nm의 사상형 바이러스 입자가 관찰되었으며 그 형태와 크기에는 두 계통간 차가 없었다.