Real Time PCR을 이용한 벼 흰잎마름병균의 밀도를 측정할 수 있는 새로운 방법을 개발하였다. Real Time PCR을 이용하여 벼 흰잎마름병을 예찰하기 위하여 TaqMan MGB probe를 이용한 프라이머인 Xan_PahgeF & Xan_PahgeR primer와 Xan_Pahge FAM MGB probe를 제작하였으며, 높은 특이성이 인정되었다. 병원균 배양액, 벼 흰잎마름병원균의 DNA, 병원세균에 오염된 물에서도 효과적으로 검출이 되었다. 농수로물이나 관개수에서 벼 흰잎마름병균의 밀도를 측정할 때 정량 PCR의 저해인자 제거 후 신속하게 벼 흰잎마름병균의 밀도를 측정할 수 있다.

In vitro high-frequency plant regeneration of Muscari comosum var. plumosum through somatic embryogenesis was obtained via two developmental pathways: direct embryos and multiple shoots regenerated from embryogenic callus. Flower bud with pedicel, receptacle, petal and ovary wall, floral stalk and leaf as explants were cultured in MS medium supplemented with various plant growth regulators. Embryos formed directly from pedicel, receptacle and floral stalk. Depending on explant sources, the optimal medium was MS medium supplemented with 0.2 mg/L IBA and 0.3 mg/L BA, 3.0 mg/L IBA and 3.0 mg/L BA, and MS-free medium for pedicel, receptacle, and floral stalk, respectively. Multiple shoots regenerated from embryogenic cal]i which was initiated from petal, ovary and leaf were observed in MS medium with different concentrations and combinations of hormone. The most suitable medium for each type of explant was 3.0 mg/L IBA and 3.0 mg/L BA(petal and ovary) and 5.0 mg/L IBA and 5.0 mg/L BA (leaf) Furthermore, the combination of 0.1 mg/L 2,4-D and 1.0 mg/L BA was also good for all sources of explants not only for direct embryo formation, but also, for embryogenic callus induction.