南京師范大學近日在《Agronomy 》發(fā)表文獻《Genome-Wide Analysis of Soybean Mosaic Virus Reveals Diverse Mechanisms in Parasite-Derived Resistance》，文獻中實驗使用了上海路陽儀器有限公司生產銷售的LUYOR-3415RG便攜式雙波長熒光蛋白激發(fā)光源，用于觀察綠色熒光蛋白GFP和紅色熒光蛋白RFP在葉片上的表達。LUYOR-3415RG內置了440-460nm藍光波段，佩戴LUV-30A熒光觀察眼鏡，可以觀察綠色熒光蛋白在動植物上的表達，同時還內置了520-530nm綠光波段，配合LUV-50A熒光觀察眼鏡，可以觀察紅色熒光蛋白（例如：tdtomato，mcherry，dsred2）在動植物上的表達，LUV-495A和LUV-590A拍照濾鏡可以配合單反相機進行熒光照片拍攝。

文獻摘要：

Plant viruses cause severe losses in agricultural production. Parasite-derived resistance (PDR) offers a promising avenue for developing disease-resistant varieties independent of resistance genes. However, for potyviruses with great agricultural importance, such as soybean mosaic virus (SMV), systematic research on viral genes that can be used for PDR has not been conducted. In this study, we transiently expressed the untranslated region (UTR) or each protein-coding cistron of SMV in Nicotiana benthamiana to evaluate their potential role in conferring PDR. A viral suppressor of RNA silencing (VSR) was also applied to investigate the possible mechanisms of the PDR. The results showed that the transient overexpression of UTR and each cistron of SMV could inhibit SMV infection. The expression of VSR in N. benthamiana leaves could compromise UTR and most of the SMV cistron-mediated inhibition of SMV infection, indicating the involvement of RNA silencing in PDR. In comparison, the expression of VSR could not compromise the PDR conferred by coat protein (CP), P3N-PIPO, cylindrical inclusion (CI), and NIa-Pro, suggesting that these viral cistrons may play roles in PDR at the protein level. These results reveal diverse mechanisms in PDR conferred by different viral cistrons and provide potential gene candidates that can be used for transgenic approaches against SMV.

2.4. Photograph and Microscopy

For assessment of the viral infection in the leaves, the GFP and RFP signals were excited using a handheld LED lamp LUYOR-3415RG (Shanghai Luyor Instrument Co., Ltd., Shanghai, China). Subsequently, the fluorescence emitted by GFP and RFP was captured using an LP510 filter or a BP590 filter (LUV-590A, Shanghai Luyor Instrument Co., Ltd., Shanghai, China), respectively, with a digital camera. In order to overlay images of the leaves with different fluorescence, Photoshop CC (version 14.0) was used to extract the RGB signals of fluorescent proteins.

文獻地址：https://doi.org/10.3390/agronomy14071457 

LUYOR-3415RG產品介紹：

中文：LUYOR-3415RG雙波長熒光蛋白激發(fā)光源

英文：Dual Fluorescent Protein Flashlight LUYOR-3415 

公司除在美國和中國設有公司外，還在加拿大、西班牙、俄羅斯等國家有授權代理商，如欲查詢當地聯系信息，請發(fā)郵件到：info@luyorgroup.com