버섯은 우리나라를 비롯한 전 세계적으로 널리 이용되고 있는 식품 중의 하나로 최근 다양한 생리 활성 효과 등 다양한 분야에서 활발하게 연구가 진행되고 있다. 본 연구는 여러 다양한 버섯 중에서 우리나라에서 식용으로 널리 이용되고 있는 새송이 버섯과 팽이버섯 추출물의 항산화 활성 및 세포독성 효과를 살펴보고자 하였다. 실험결과, 새송이버섯과 팽이버섯추출물의 총 페놀 함량은 각각 19.60±0.10 mg/g 과 22.28±1.10 mg/g으로 나타났으며, 플라보노이드 함량은 각각 15.21±1.31, 20.51±4.52였다. 2.5, 5.0, 7.5, 10.0 mg/mL 농도에서의 DPPH radical 소거능은 새송이버섯과 팽이버섯 각각 2.5 mg/mL의 농도에서 7.98±0.58, 8.71±0.45였고, 10 mg/mL 농도에서 각각 35.35±0.52, 39.39±0.26으로 고농도에서 높은 DPPH 라디컬 소거능을 보여주었다. 환원력은 10 mg/mL의 농도에서 각각 1.417±0.011, 1.171±0.006으로 시료의 농도가 증가할수록 흡광도 값도 증가하여, 높은 환원력을 보여주었다. 새송이버섯 추출물과 팽이버섯 추출물의 인간 정상 신장세포 HEK293으로 본 정상세포에 대한 세포독성을 측정한 결과에서는 새송이버섯, 팽이버섯 추출물 모두 80%의 생존력을 나타내어 독성이 없는 것으로 보여진다. 한편, 위암세포, 유방암세포 및 간암세포에서 암세포 성장억제율이 높게 나타나 항암 효과의 가능성을 보여주었다.

팽이의 신품종을 개발하기 위하여 모균주 ASI 4216(한솔)과 4217(백중)으로부터 단포자를 분리하여 단핵균주를 얻고 이들의 교잡을 통해서 꺽쇠연결체가 확인된 교잡주 총 129점을 선발하였다. 교잡주를 대상으로 3회에 걸쳐 재배시험 결과, 고온에서 배양이 가능하며 수량성이 우수한 계통 ‘Fv14a51’을 최종선발되었으며, 생산력검정 시험을 통해 2017년 농작물 직무육성 품종 심의회에서 ‘백이’로 명명되었다. 주요 특성은 균사생장이 30°C의 고온에서도 균활력을 유지할 정도로 강한 온도적응성 품종이고 대조품종에 비해 갓이 두껍고 대가 얇는 형태를 띠는 것 외에는 갓색깔이 순백색이며, 갓모영은 반구형, 수량은 257.4±13.5g으로 대조품종과 비교해서 대체적으로 유사 하였다. RAPD primer을 통해 유전적 다형성을 검정한 결과, 대조구인 ‘오키노메구미’, 2016년에 육성된 ‘백승’과 신품종이 유전적으로 구별되는 것을 확인하였다. 전반적으로 ‘백이’는 수량과 품질이 외국품종과 거의 유사하였으며, 버섯의 균일한 형태로 상업적 가치가 있었다. 신품종의 현장실증을 확대하여 국산품종이 국내에 확산되기를 기대한다.

팽이버섯 ‘금향2호’는 2013년도 느타리 봉지재배 농가의 시범재배 과정에서 ‘갈뫼’와 우리원 육성품종 ‘금향’이 자연교잡된 개체를 조직분리함으로써 육성된 품종으로, 갓 색이 진한 미색을 나타내며, 비닐고깔을 씌우지 않고 재배가 가능하여 노동력이 절감되는 장점이 있다. 16℃ 고온에서 비닐고깔을 씌우지 않고 병재배 시 배양 기간은 24일, 초발이 소요일수는 8일, 생육일수는 11일로 총재배기간이 43일 소요되어 대조품종 ‘금향’에 비해 2일 증가되었다. 갓 색은 진한 미색으로 ‘금향’과 매우 유사했으나, 갓 직경이 더 작고 갓 두께와 대 직경이 더 굵었다. 850 ml(Φ59) 병당 수량은 118 g으로 비닐고깔을 씌운 재배방식에 비해서는 현저히 감소하였으나, 품질이 양호하여 느타리버섯 병재배 농가에 접목 시 노동력 절감 가능성을 보여 주었다.

팽이버섯 신품종‘여름향1호’는 ‘갈뫼’와 ‘건국1호’로부터 분리한 단포자를 교배함으로써 육성된 품종으로, 갓색이 연한 갈색을 나타내며, 고온성이면서 재배기간이 짧은 장점이 있다. 16℃ 고온에서 병재배 시 배양 기간은 22일, 초발이 소요일수는 6일, 생육일수는 10일로 총재배 기간이 38일이 소요되어 대조품종 '금향'에 비해 3일, ‘갈뫼’에 비해 7일이 단축되었다. 특히 버섯 발생이 빠르면서도 균일성이 우수하였으며, 갓 색은 진한 미색인 ‘금향’과 중간 갈색인 ‘갈뫼’의 중간 수준인 연한 갈색을 띠었다. 수량은 850 ml(Φ59) 병 당 138 g으로 '금향' 대비 10% 증수되었다.

팽이버섯 신품종 ‘여름향2호’는 ‘갈뫼’와 우리원 육성품종 ‘흑향’으로부터 분리한 단포자를 교배함으로써 육성된 품종으로, 갓 색이 흑갈색을 나타내며, 고온성이면서 재배 기간이 짧은 장점이 있다. 16°C 고온에서 병재배 시 배양 기간은 24일, 초발이 소요일수는 8일, 생육일수는 8일로 총재배기간이 40일 소요되어 대조품종 ‘흑향’에 비해 3일 단축되었다. 특히 초발이 소요일수가 2일 단축되면서도 버섯 발생이 균일한 특성을 보였다. 수량은 850 ml(∅59) 병 당 154 g으로 ‘흑향’에 비해 8% 증수되었다. 베타글루칸 함량은 67.89 g/ 100g으로‘흑향’, 시판 중인 황금팽이, 백색 팽이버섯에 비해서 1.1~2.2배 높았다.

This study was conducted to investigate the effects of fermented spent mushroom substrates (F-SMS) of Flammulina velutipes on growth performance, carcass traits, and economic characteristics of Hanwoo steers. A yeast strain (Saccharomyces sp. UJ14) and Bacillus strain (Bacillus sp. UJ03) isolated from fresh spent mushroom substrates of Flammulina velutipes were used as probiotics to prepare F-SMS. Twenty-four Hanwoo steers (14 months old) were allocated to three dietary treatments via a randomized block design and were slaughtered at 30 months of age. These treatment groups included Control (TMR), T1 (TMR containing 10% of F-SMS) group, and T2 (TMR containing 30% of F-SMS). Body weight gain was not influenced by the experimental diets. DM and TDN intakes in the finishing period were significantly (p < 0.05) greater in group T1 than in other groups. CP intake was significantly (p < 0.05) greater in group T2 than in other groups during the whole experimental period. Among carcass traits, rib-eye area and back fat thickness tended to increase with F-SMS supplementation. The appearance rate (%) of a meat yield more than grade A was the highest in group T1. The net profits increased by 1.2% and 13.3% in groups T1 and T2, respectively. In conclusion, if a proper feeding program (including feed safety) can be ensured, spent mushroom substrates of Flammulina velutipes can prove to be a highly profitable feed source for Hanwoo steers.

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.

Diets rich in flavonoid-containing foods are sometimes associated with cancer, neurodegenerative and cardiovascular disease prevention. β-glucan, one of the most important bioactive compounds in medicinal mushrooms, is used to boost the immune system, diabetes and cancer. In this study, we aimed to determine the content of two flavonoid compounds (naringenin and naringin) and β-glucan in Flammulina velutipes and Flammulina velutipe-gold strain. The naringenin, naringin, and β-glucan components from the Flammulina velutipes and Flammulina velutipe-gold strain were measured by the HPLC analysis. As a result, the contents of naringenin, naringin, and β-glucan were found to be much higher in Flammulina velutipe-gold strain than Flammulina velutipe. From the above results, we may suggest that Flammulina velutipe-gold strain might have useful as a material for functional food and pharmaceutics fir the pathological process of various human diseases.

본 연구는 팽이버섯 수확 후 배지를 첨가하여 호밀 사일리지 제조 시 팽이버섯 수확 후 배지를 에너 지원으로서 사용하기 위하여 in vitro 반추위 발효실험이 수행되었다. 공시 사일리지는 출수기의 호밀 에 팽이버섯 수확 후 배지 첨가비율(0%, 20%, 40%, 60%)에 따라 제조하여 6주일간 발효시켰다. In vitro 배양액 제조를 위한 반추위액은 농후사료와 볏짚을 40:60의 비율로 급여한 반추위 cannula가 시 술된 Holstein 수소 2두로 부터 채취하였다. In vitro 실험은 발효시간대를 3, 6, 9, 12, 24 및 48시간 으로 설정하고, 각 처리구별로 3반복으로 발효특성과 건물소화율을 측정하였다. In vitro 배양액의 pH 는 발효시간이 길어짐에 따라 낮아지는 경향이었으며, 48시간 경과 시에는 버섯수확 후 배지 60% 첨가 구가 타 처리구에 비해 유의적(p<0.05)으로 낮았다. 미생물 성장율은 배양시간이 경과함에 따라 증가 하는 경향이었으며, 발효 48시간 경과 시에는 버섯수확 후 배지 20% 첨가구가 타 처리구에 비해 유의 적으로(p<0.05) 높았다. Gas발생량은 48시간 발효 시에 대조구가 타 처리구에 비해 유의적(p<0.05)으 로 높았다. 건물소화율은 버섯수확 후 배지의 첨가비율이 높을수록 높았는데, 발효 24시간 및 48시간에 는 R-60구가 처리구 중에서 가장 높았으며(p<0.05), 대조구에서는 전 발효기간 동안 건물소화율이 현 저히 낮은(p<0.05) 상태에 있었다. In vitro 반추위내 발효실험의 결과와 버섯수확 후 배지의 활용성을 고려할 때, 호밀사일리지 제조 시 팽이버섯 수확 후 배지 첨가비율을 원물기준으로 60%수준이 가장 긍 정적인 것으로 나타났다. 향후 대사시험이나 사양시험을 통하여 가축사료로써의 최적 대체 비율을 규명 해야 할 것으로 사료되는 바다.

Microsatellite SSR markers were developed and utilized to reveal the genetic diversity of 32 strains of Flammulina velutipes collected in Korea, China, and Japan. From the SSR-enriched library, 490 white colonies were randomly selected and sequenced. Among the 490 sequenced clones, 85 (17.35%) were redundant. Among the remaining 405 unique clones, 201 (49.6%) contained microsatellite sequences. We used 12 primer pairs that produced reproducible polymorphic bands for four diverse strains, and these selected markers were further characterized in 32 Flammulina velutipes strains. A total of 34 alleles were detected using the 12 markers, with an average of 3.42 alleles, and the number of alleles ranged from two to seven per locus. The major allele frequency ranged from 0.42 (GB-FV-127) to 0.98 (GB-FV-166), and values for observed (HO) and expected (HE) heterozygosity ranged from 0.00 to 0.94 (mean = 0.18) and from 0.03 to 0.67 (mean = 0.32), respectively. SSR loci amplified with GB-FV-127 markers gave the highest polymorphism information content (PIC) of 0.61 and mean allele number of five, whereas for loci amplified with GB-FV-166 markers these values were the lowest, namely 0.03 and two. The mean PIC value (0.29) observed in the present study with average number of alleles (3.42). The genetic relationships among the 32 Flammulina velutipes strains on the basis of SSR data were investigated by UPGMA cluster analysis. In conclusion, we succeeded in developing 12 polymorphic SSRs markers from an SSR-enriched library of Flammulina velutipes. These SSRs are presently being used for phylogenetic analysis and evaluation of genetic variations. In future, these SSR markers will be used in clarifying taxonomic relationships among the Flammulina velutipes.

Microsatellite SSR markers were developed and utilized to reveal the genetic diversity of 32 strains of Flammulina velutipes collected in Korea, China, and Japan. From SSR-enriched library, 490 white colonies were randomly selected and sequenced. In the 490 sequenced clones, 85 clones (17.35%) were redundant. Among the remaining 405 unique clones, 201 clones (49.6%) contained microsatellite sequences. As a result, 12 primer pairs produced reproducible polymorphic bands within diverse 4 strains and these selected markers were further characterized in 32 Flammulina velutipes strains. A total of 34 alleles were detected using the 12 markers, with an average of 3.42 alleles and the number of alleles ranged from two to seven per locus. The major allele frequency ranged from 0.42 (GB-FV-127) to 0.98 (GB-FV-166), and values for observed (HO) and expected (HE) heterozygosity ranged from 0.00 to 0.94 (mean = 0.18) and from 0.03 to 0.67 (mean = 0.32), respectively. SSR loci amplified with GB-FV-127 markers gave the highest polymorphism information content (PIC) of 0.61 and mean allele number of five, while for loci amplified with GB-FV-166 markers these values were the lowest, namely 0.03 and two. The mean PIC value (0.29) observed in the present study with average number of alleles (3.42). The genetic relationships among 32 Flammulina velutipes strains based on SSR data were generated by UPGMA cluster analysis. In conclusion, we succeeded in developing 12 polymorphic SSRs markers from SSR-enriched library of Flammulina velutipes. These SSRs are presently being used for phylogenic analysis and evaluation of genetic variations. In future, these SSR markers will be used in clarifying taxonomic relationships among the Flammulina velutipes.

‘Baekseung’, a new variety of Flammulina velutipes, was bred by mating two monokaryotic strains isolated from KMCC 4210 and KMCC 4216 in the Mushroom Research Division, Baekseung ARES in 2016. The Baekseung and Uri1ho strains showed fast mycelial growth and mycelial density on malt extract agar media after 7 days of incubation. The spawn running period on the sawdust substrate required a cultivation period and temperature of 30 days and 25oC, respectively, for primordia formation where in fruiting body development occurred from 11±1 days at 14oC and 14±1 days at 7oC. The length of the pilei and stipes of the Baekseung harvested in optimal stag were 11.3±0.4 and 89.2±7.1 mm, respectively, whereas the values for Uri1ho were 10.7±1.0 and 91.3±20.8 mm, respectively. The yield of the Baekseung and Uri1ho strain grown on the sawdust substrate was 153.7±12.5 and 139.8±17.8 g, respectively, per 850 ml in bottle cultivation. The inferred tree exhibited a phylogenetic relationship between the Korean white fruiting body strains of Baekseung, Uri1ho and Fv-14-a-38, Fv-14-a-51, and the Japanese white fruiting body-forming strains of KMCC 4226, and these were confirmed to be genetically related.

NGS data was yielded by using Illumina Hiseq platform. The short reads were filtered by quality score and read length were mapped against the reference genome (KACC42780). Genome-wide reanalyzed data of Flammulina strains were compared against the reference genome to establish a genome-wide single nucleotide polymorphism (SNP). The rate of mapping differences between the strains reflected in the strain variation in its result. The genome-wide SNPs distribution divided into types of homozygous SNP and heterozygous SNP moreover all of the strains demonstrated a wide variation in all of the regions. In the further study of topological relationship between the collected strains, phylogenetic tree was separated into 3 major groups. Group I contained F. velutipes var. related strains of ASI 4062, 4148, 4195. Group Ⅱ contained strains that were different species of ASI 4188 F. elastica, ASI 4190 F. fennae, and ASI 4194 F. rossica. The other 19 strains F. velutipes were classified as a single group. Polymorphic SNPs of F. velutipes strains representing the phylogenetic segregation of whiteand brown-fruiting body forming groups were compared. As previously reported, white gene expression is recessive to brown in fruiting body color gene expression. The white strains produced 131,874 SNPs to be aa type and homozygous from of SNP. 407,947 SNPs were detected as AA, Aa type from the brown-fruiting body of SNP. We constructed a SNP matrix with 8 white strains and 12 brown strains. To develop the molecular marker related in to fruiting body color and geographical origin, we isolated 240 SNPs from the white-and brown-fruiting body forming. To determine the chromosome relationship on polymorphic SNP between Korea and Japan strains producing white-fruiting body, we analyzed that the Korea white strains detected 185,695 SNPs and the Japan white strains produced 263,811 SNPs. Using the constructed SNP matrix with 3 Korea white strains and 3 Japan white strains, the experiment generated 475 SNPs of phylogenetic SNPs fromKorea and Japan white-fruiting body. As a result, we regarded as they are potentially related to the white color. White and brown color and origin specific SNPs could be used as an identification marker for selection of F. veluipes strains in the breeding program.

본 연구에서는 버섯 수확후배지를 바이오매스로 활용하 고자 수행하였으며, 적정 전처리 조건을 구명한 결과는 다음과 같다. 버섯 수확후 배지의 전처리방법 중 알카리 처리가 리그닌 함량을 효과적으로 경감시키면서, 당전환 율이 우수하였고 큰느타리 수확후 배지가 당전환율 80.7%로 가장 우수하였다. 큰느타리 수확후 배지에 1% NaOH를 이용한 알카리 처리시 전처리 온도별 성분분석 결과 120℃처리시에 glucose 25.3%, xylose 14.8%로 유 리당 함량이 가장 높고, 효소에 의한 당전환율도 66%로 무처리구 28.2%에 비해 2.3배 증가되었다. 촉매제 농도 (NaOH 0.5~2.0%)에 따른 당분석결과 glucose 함량은 촉 매제 농도와 관계가 적었으며, xylose와 arabinose는 촉매제 농도가 높을수록 다소 감소하는 경향이었다. 그러나 당전환율은 NaOH 1% 처리시에 66%로 가장 높았다.

팽이버섯 포장필름의 국산화 및 동남아시아 지역을 대 상으로 한 수출용 필름을 개발하기 위하여, 개발된 포장 필름을 현재 시중에 유통 중인 포장필름 및 수입산 포장 필름과 함께 저장 중 팽이버섯의 저장 온도별 품질변화에 이어 유리당, 유리아미노산, 구성아미노산 등에 대한 영양 학적 특성변화를 검토하였다. 유리당 함량을 분석한 결과, 저장 온도가 높아질수록 유리당 함량이 약간씩 증가하는 경향을 보였으나, 포장 필름의 종류에 따라서는 큰 차이 를 나타내지 않았다. 유리아미노산의 경우 저장온도가 올 라감에 따라 methionine은 증가하는 반면, tyrosine은 감 소하였다. Polyphenol oxidase의 활성 확인결과 본 과제 로 인해 개발된 포장지가 우수함을 확인하였다. 베타글루 칸 함량은 건강 기능성 식품의 표준 지표로 사용되는 성 분이나 버섯 저장성을 판단하는 지표로 사용하기에는 적 당하지 않을 것으로 여겨진다.

The mannanase-producing bacteria, designated YJ17, was isolated from spent mushroom (Flammulina velutipes) substrates. The isolate YJ17 was a facultative anaerobic and was grown at temperatures ranging from 20oC to 50oC with an optimal temperature of 40oC. The DNA G+C content of the YJ17 was 44 mol%. The major fatty acids were anteiso-15:0 (38.9%), 17:0 (7.6%), and iso-15:0 (36.5%). The 16S rRNA gene sequence similarity between the isolate YJ17 and other Bacillus strains was from 98% to 99%. In the phylogenetic analysis based on these sequences, the isolate YJ17 and Bacillus amyloliquefaciens clustered within a group together and separated from other species of Bacillus. Based on the physiological and molecular properties, the isolate YJ17 was classified within the genus Bacillus as B. amyloliquefaciens YJ17. The optimal pH and temperature for mannanase activity of B. amyloliquefaciens YJ17 were pH 7.0 and 50oC, respectively.

This study was conducted to establish replacement the corncob used in winter mushroom bottle cultivation. Corncob is unstable quality in moisture content or total nitrogen(T-N) content. Fruit body yields according to the ratio of cassava stem chips mixing were compared. After treatment-1 and treatment-2, fruit body yields increased by 8.8% and 5.4% and raw material cost decreased by 7% and 19%. The results showed that cassava stem chips could replace 33% to 67% of corncob for winter mushroom bottle cultivation.

The aim of this study was to identify and characterize new Flammulina velutipes laccases from its whole-genome sequence. Of the 15 putative laccase genes detected in the F. velutipes genome, four new laccase genes (fvLac-1, fvLac-2, fvLac3, and fvLac-4) were found to contain four complete copper-binding regions (ten histidine residues and one cysteine residue) and four cysteine residues involved in forming disulfide bridges. fvLac-1, fvLac-2, fvLac3, and fvLac-4, encoding proteins consisting of 516, 518, 515, and 533 amino acid residues, respectively. Potential N-glycosylationsites(Asn-Xaa-Ser/Thr) were identified in the cDNA sequence of fvLac-1(Asn-454), fvLac-2(Asn- 437andAsn-455), fvLac-3(Asn-111andAsn-237), and fvLac4 (Asn-402andAsn-457). In addition, the first 19–20 amino acid residues of these proteins were predicted to comprise signal peptides. Laccase activity assays and reverse transcription polymerase chain reaction(RT-PCR) analyses clearly reveal that CuSO4 affects the induction and the transcription level of these laccase genes.

This study was conducted to obtain a growth correlation of basal information from the development of disease resistantFlammulina velutipes cultivars through back-crossing between the strains of wild-type brown monokaryon 4019-20 and thederivative of commercial quality white monokaryons 3. The two strains were selected to back-cross for further enhancing their latentattributes and growth characteristics. The parents of 4019-20×M3 back-crossed to reproduce F1, M3-Sn. Using F1, M3-Sn procuredand isolated into 94 monokaryon strains. Further examination of growth characteristics carried out by back-crossing between M3and BC1F1 from M3-n dikaryon. Monokaryon exhibited an irregular growth pattern and demonstrated to be sluggish development inthe sawdust medium. However BC1F1(M3-n) dikaryon strains confirmed mostly regular growth pattern and demonstrated ordinarygrowth in the sawdust medium. The fruitbody of BC1F1 confirmed as light-brown colour to be the dominant gene. The colourdistributions of fruitbody, BC1F1, resulted as follows; 7% of dark brown, 25% of brown , 27% of light brown, 16% of ivory and 25%of white. The ratio of the other color to white showed 3 to 1 which suggested two major genes were related to fruitbody color.

‘Baekjung’ adaptable to high temperature was made by crossing between monokaryon derived from selfing of brownstrain and monokaryon derived from Korea white strain. In the condition that temperature is maintained at 10oC without lowtemperature of 4oC suppressing treatment and wrapping during cultivation period, it showed good productivity thanUri1ho(control). The optimum temperature of mycelial growth was 30oC and that of fruiting body initiation and developmentwere 14oC and 7oC, respectively. The days for the fruiting and yield were 7days and 277±11.2g per 1,100ml bottle,respectively. This variety needed high concentration of carbon dioxide up to 4,000 ppm for the good quality.