• 한국작물학회지
• /
• 제62권1호
• /
• pp.1-8
• /
• 2017

벼 직파재배에서 새 피해, 발아 및 입모불량 그리고 도복피해 등 기술보급저해요인을 해소하기 위하여 개발된 규산 코팅볍씨의 이앙용 상자육묘에서 건묘육성과 벼키다리병 발병 경감을 구명하기 위하여 호기조건인 상자육묘조건과 혐기조건인 Pot이앙조건으로 수행한 결과는 다음과 같다. 1. 코팅볍씨에서 묘의 출현은 무코팅볍씨에서 보다 2-3일 빨랐고 입고병과 벼키다리병 발생이 현저히 경감되었다. 2. 파종후 45일 생체중은 건전묘에서 11%, 이병묘에서 2.01배로 규산코팅볍씨의 건묘 육성효과가 뚜렷하였다. 3. 육묘 중 파종후 80일까지 벼키다리병 발생은 무코팅볍씨 91.6%에 비하여 7.8%로 현저하게 경감되었다. 4. 최대발병률을 보인 파종 후 45일에 이앙된 코팅볍씨에서 무코팅볍씨에 비하여 건전묘의 추가발병이 거의 없었고 이병묘의 정상생육 회복도 가능하였다. 5. 코팅볍씨에서 육묘된 토양과 식물체의 뿌리와 엽초기부조직에서 활동성 소형포자와 대형포자의 분포가 무코팅에서보다 현저하게 줄었다. 특히 코팅볍씨의 육묘토양과 이병묘/건전묘에서는 무코팅볍씨에서 나타난 전형적인 대형포자(3-7개의 격막과 양끝이 낫처럼 굽은)와는 다른 격막이 없고 두터운 세포벽을 갖는 장방형 미성숙 대형포자 출현이 발병 경감원인으로 주목되었다. 6. 이상의 결과를 종합하여 보면 코팅볍씨의 육묘 중 벼키다리병 발병경감과 이앙 후 이병묘의 정상생육 회복 그리고 건전묘의 이병화경감은 강알칼리성 수용성 규산과 다공성 지오라이트 그리고 종피 잠복 병원균 간의 물리화학적 특성과 건전묘의 균에 대한 저항성에 기인되었을 것으로 판단되었다.

• Mycobiology
• /
• 제43권4호
• /
• pp.373-383
• /
• 2015

Five halophytic plant species, Suaeda maritima, Limonium tetragonum, Suaeda australis, Phragmites australis, and Suaeda glauca Bunge, which are native to the Muan salt marsh of South Korea, were examined for fungal endophytes by sequencing the internal transcribed spacer (ITS) region containing ITS1, 5.8S rRNA, and ITS2. In total, 160 endophytic fungal strains were isolated and identified from the roots of the 5 plant species. Taxonomically, all 160 strains belonged to the phyla Ascomycota, Basidiomycota, and Zygomycota. The most dominant genus was Fusarium, followed by the genera Penicillium and Alternaria. Subsequently, using 5 statistical methods, the diversity indices of the endophytes were determined at genus level. Among these halophytic plants, P. australis was found to host the greatest diversity of endophytic fungi. Culture filtrates of endophytic fungi were treated to Waito-C rice seedlings for plant growth-promoting effects. The fungal strain Su-3-4-3 isolated from S. glauca Bunge provide the maximum plant length (20.1 cm) in comparison with wild-type Gibberella fujikuroi (19.6 cm). Consequently, chromatographic analysis of the culture filtrate of Su-3-4-3 showed the presence of physiologically active gibberellins, $GA_1$ (0.465 ng/mL), $GA_3$ (1.808 ng/mL) along with other physiologically inactive $GA_9$ (0.054 ng/mL) and $GA_{24}$ (0.044 ng/mL). The fungal isolate Su-3-4-3 was identified as Talaromyces pinophilus.

• 한국자원식물학회:학술대회논문집
• /
• 한국자원식물학회 2020년도 추계국제학술대회
• /
• pp.65-65
• /
• 2020

Bakanae disease, caused by Gibberella fujikuroi, is one of the most devastating diseases threatening rice production in Korea. In recent years, the incidence of bakanae disease became alarming due to the mechanical transplanting practice where the spread of bakanae can be amplified during accelerating seeds growth, due to the use of seeding boxes. The development of resistant rice cultivars could be the primary and effective method for controlling bakanae disease. However, the effects of individual resistance genes are relatively small. Therefore, pyramiding of bakane R genes in rice breeding is a promising strategy having a high potential to mitigate the advert effects of bakanae disease. This study employed a gene pyramiding approach to develop bakanae disease resistant rice lines carrying qBK1, qFfR1 introduced from rice line MY299BK and cv. Nampyeong, respectively. The MY299BK carries qBK1 introduced from cv. Shingwang, which was found to have a high resistance compare to Nampyeong. In addition, the pyramiding effect of the qBK1 and qFfR1 resistance genes were investigated, and the presence or absence of these genes helped us investigate their interaction through bioassay method and MAS. Furthermore, the distribution of resistance in the population showed a biased distribution toward resistance in the F6:7 populutions. However, we could not confirm the accumulation effect of the resistance gene, but the difference between the two genes by the SN2 marker was confirmed. Therefore, the qBK1 gene harbored by MY299BK appears to be different from the qFfR1 carried by Nampyeong, suspected to possess a different bakanae disease resistant gene different from those found in MY299BK and Nampyeong.