[1] 唐孝青,李斌,伍小兵,等.绿色荧光蛋白及其应用的研究进展[J].陕西农业科学,2007,53(1):123-145. [2] 张彩霞,李壮,陈莹,等.植物与病原菌互作的蛋白质组学研究进展[J].西北植物学报,2010,30(3):626-632. [3] 赵志文,李艳娇,户勋,等.用于植物病原细菌标记的pBB-GFP载体构建及应用[J].生物技术通报,2018,34(3):136-141. [4] 杨雷. 利用绿色荧光蛋白基因标记核盘菌菌丝[D].哈尔滨:哈尔滨工业大学,2006. [5] SHIMOMURA O,JOHNSON F H,SAIGA Y.Extraction,purification and properties of aequorin,a bioluminescent protein from theluminous hydromedusan,Aequorea[J].Journal Celularl and Comparative Physiology,1962,59:223-239. [6] PRASHER D C,ECKENRODE V K,WARD W W,et al.Primarystructure of the Aequorea victoria green-fluorescent protein[J].Gene,1992,111(2):229-233. [7] CHALFIE M,TU Y,EUSKIRCHEN G,et al.Green fluorescent protein as a marker for gene expression[J].Science,1994,263(5148):802-805. [8] HEIM R,PRASHER D C,TSIEN R Y.Wavelength mutations and posttranslational autoxidation of green fluorescent protein[J].Proceedings of the National Academy of Sciences,1994,91(26):12501-12504. [9] 张海洋. 外源基因在银耳芽孢中的高效表达体系研究及应用[D].福州:福建农林大学,2018. [10] 陈赟娟,韦建福.丝状真菌遗传转化的研究进展[J].云南农业大学学报,2009,24(3):448-454. [11] CAMPOY S,PÉREZ F,MARTIN J F,et al.Stable transformants of the azaphilone pigment-producing monascus purpureus obtained by protoplast transformation and agrobacterium-mediated dna transfer[J].Current Genetics,2003,43(6):447-52. [12] SCHIESTL R H,PETES T D.Integration of DNA fragments by illegitimate recombination in Saccharomyces cerevisiae[J].Proceedings of the National Academy of Sciences,1991,88(17):7585-7589. [13] 李娟,杨金奎,梁连铭,等.丝状真菌遗传转化系统研究进展[J].江西农业大学学报,2006,28(4):516-520. [14] KHAN M,TABE L M,HEATH L C,et al.Agrobacterium-mediated transformation of subterranean clover (Trifolium subterraneum L.)[J].Plant Physiology,1994,105(1):81-88. [15] 陈孝仁,程保平,王新乐,等.利用绿色荧光蛋白研究大豆疫霉与大豆的互作[J].科学通报,2009,54(13):1894-1901. [16] 宿景霞. GFP标记溶磷细菌在葡萄根际的定殖研究[D].杨凌:西北农林科技大学,2012. [17] 张鑫,刘爱芬,张玮,等.葡萄溃疡病菌限制性内切酶介导整合方法的建立及转化子库的构建[J].微生物学通报,2013,40(7):1272-1278. [18] 王军,付爱根,徐敏,等.基因枪法在遗传转化中的研究进展[J].基因组学与应用生物学,2018,37(1):459-468. [19] GU B,KALE S D,WANG Q H,et al.Rust secreted protein Ps87 is conserved in diverse fungal pathogens and contains a RXLR-like motif sufficient for translocation into plant cells[J].PloS One,2011,6(11) :e27217. [20] OLMEDO-MONFIL V,CORTÉS-PENAGOS C,HERRERA-ESTRELLA A.Three decades of fungal transformation[J].Recombinant Gene Expression:Reviews and Protocols,2004,267:297-313. [21] 赵凤轩. 绿色荧光蛋白标记的大丽轮枝菌的获得及其在棉花中侵染过程研究[D].北京:中国农业科学院,2010. [22] 贾娜娜. 梨腐烂病菌GFP标记及其在梨组织中侵染的显微观察病原菌侵染方式[D].武汉:华中农业大学,2015. [23] SEXTON A C,HOWLETT B J.Green fluorescent protein (GFP) as a reporter in the Brassica-Leptosphaeria maculans[J].Molecular Plant Pathology,2001,58:13-21. [24] 陶恺. 大豆疫霉侵染过程的分子细胞学研究[D].南京:南京农业大学,2012. [25] 韩小路. PEG介导的苹果果生刺盘孢Colletotrichum fructicola原生质体转化体系的研究[D].杨凌:西北农林科技大学,2015. [26] 张键. 向日葵大丽轮枝菌T-DNA突变体库的建立及微菌核形成和致病力相关基因的研究[D].呼和浩特:内蒙古农业大学,2016. [27] 姚锦爱,张鸿,黄鹏,等.建兰茎腐病原菌尖孢镰刀菌F02的绿色荧光蛋白基因标记[J].福建农业学报,2019,34(1):70-75. [28] 孙洪宝,吕桂云,许勇.绿色荧光蛋白(GFP)标记的尖孢镰刀菌在西瓜抗、感寄主根系中侵染和定殖[J].中国瓜菜,2019,32(8):200-201. [29] MAOR R,PUYESKY M,HORWITZ B A,et al.Use of the green fluorescent protein (GFP) for studying development and fungal-plant interaction in Cochliobolus heterostrophus[J].Mycological Research,1998,102(4):491-496. [30] CHEN N,HSIANG T,GOODWIN P H.Use of green fluorescent protein to quantify the growth of Colletotrichum during infection of tobacco[J].Journal of Microbiological Methods,2003,53(1):113-122. [31] 钟卫鸿,叶海仁,陈建孟,等.应用绿色荧光蛋白基因标记细菌进行生物膜结构定量化新方法[J].环境科学,2005,26(4):160-164. [32] 吴春利,刘洁生,杨维东.绿色荧光蛋白及其在细胞生物学研究中的应用[J].细胞生物学杂志,2002,24(4):226-230. [33] RIEDEL M,CALMIN C Z,BELBAHRI L,et al.Green fluorescent protein (GFP) as a reporter gene for the plant pathogenic oomycete Phytophthora ramorum[J].Eukaryot Microbiol,2009,56(2):130-135. [34] AUDREY M V,AH-FONG,JUDELSON H S.Vectors for fluorescent protein tagging in Phytophthora:tools for functional genomics and cell biology[J].Fungal Biology,2011,115(9):882-890. [35] 郭晓宇,李玲,董波,等.利用荧光蛋白标记研究稻瘟病菌有性世代的细胞结构[J].中国细胞生物学学报,2018,40(7):1138-1145. |