[1] Mansfield J, Genin S, Magori S, et al. Top 10 plant pathogenic bacteria in molecular plant pathology[J]. Molecular Plant Pathology, 2012, 13(6):614-629. [2] Genin S, Boucher C. Lessons learned from the genome analysis of Ralstonia solanacearum[J]. Annual Review Phytopathology, 2004, 42:107-134. [3] Schell M A. Control of virulence and pathogenicity genes of Ralstonia solanacearum by an elaborate sensory network[J]. Annual Review of Phytopathology, 2000, 38:263-292. [4] 张勇, 李牧原, 罗锋. 青枯菌三型分泌系统研究进展[J]. 微生物学报, 2015, 55(6):675-682. [5] Li S, Su Y, Chen J, et al. Evaluation of the antibacterial effects and mechanism of action of protocatechualdehyde against Ralstonia solanacearum[J]. Molecules, 2016, 21(6):754. [6] 黎起秦, 叶云峰, 蒙显英, 等. 内生细菌B47菌株的鉴定及其对番茄青枯病的防效测定[J]. 中国生物防治, 2005, 21(3):178-182. [7] 胡菁. 恶臭假单胞菌A1在番茄青枯病生物防治中的应用[D]. 福州:福建农林大学, 2017. [8] Sijam K, Dikin A. Biochemical and physiological characterization of Burkholderia cepacia as biological control agent[J]. International Journal Agriculture Biology, 2005, 7(3):385-388. [9] Johunson S L, Bishop-Lilly K A, Ladner J T, et al. Complete genome sequences for 59Burkholderia isolates, both pathogenic and near neighbor[J]. Genome Announcements, 2015, 3(2):1-3. [10] Haas D, Défago G. Biological control of soil-borne pathogens by fluorescent pseudomonads[J]. Nature Reviews Microbiology, 2005, 3:307-319. [11] Sambrook J, Fritsch E F, Maniatis T. Molecular Cloning:A Laboratory Manual[C]. New York:Cold Spring Harbor Laboratory Press, 1989. [12] Simon R, Priefer U, Pühler A. A broad host range mobilization system for in vivo genetic engineering:transposon mutagenesis in gram negative bacteria[J]. Biotechnology, 1983, 1(9):784-791. [13] 方中达. 植病研究方法(第三版)[M]. 北京:中国农业出版社, 2007. [14] 东秀珠, 蔡妙英. 常见细菌系统鉴定手册[M]. 北京:科学出版社, 2001. [15] Marchesi J R, Sato T, Weightman A J, et al. Design and evaluation of useful bacterium-specific PCR primers that amplify genes coding for bacterial 16S rRNA[J]. Applied Environmental Microbiology, 1998, 64(2):795-799. [16] 冯震, 杨燕, 张宁, 等. 基于gyrB基因的伯克霍尔德菌属核酸测序鉴定与系统进化分析[J]. 药物分析杂志, 2019, 39(11):1940-1944. [17] 迟晓丽, 刘珂欣, 许超, 等. 番茄土传病害拮抗菌的筛选、鉴定及拮抗性能评价[J]. 中国农学通报, 2020, 36(3):135-141. [18] 张立新, 苏婷, 谢关林. 洋葱伯克氏菌群不同基因型菌株对几种重要植物病原真菌的抑制作用及其潜在致病性[J]. 中国生物防治, 2009, 25(1):25-29. [19] 张清霞, 张迎, 何玲玲, 等. 水稻纹枯病拮抗细菌7-5的鉴定及其生防机制初步研究[J]. 中国水稻科学, 2018, 32(3):277-284. [20] Howell C R, Stipanovic R D. Control of Rhizoctonia solani on cotton seedlings with Pseudomonas fluorescens and with an antibiotic produced by the bacterium[J]. Phytopathology, 1979, 69:480-482. [21] Castric K F, Castric P A. Method for the rapid detection of cyanogenic bacteria[J]. Applied Environmental Microbiology, 1983, 45(2):701-712. [22] 魏海雷, 王烨, 张力群, 等. 生防菌株2P24与CPF-10的鉴定及其生防相关性状的初步分析[J]. 植物病理学报, 2004(1):80-85. [23] Schwyn B, Neilands J B. Universal chemical assay for the detection and determination of siderophores[J]. Analytical Biochemistry, 1987, 160(1):47-56. [24] Reimmann C, Beyeler M, Latifi A, et al. The global activator GacA of Pseudomonas aeruginosa PAO positively controls the production of the autoinducer N-butyryl-homoserine lactone and the formation of the virulence factors pyocyanin, cyanide and lipase[J]. Molecular Microbiology, 1997, 24(2):309-319. [25] Herrero M, De L V, Timmis K N. Transposon vectors containing non-antibiotic resistance selection markers for cloning and stable chromosomal insertion of foreign genes in gram-negative bacteria[J]. Journal of Bacteriology, 1990, 172(11):6557-6567. [26] Kolibachuk D, Miller A, Dennis D. Cloning, molecular analysis, and expression of the polyhydroxyalkanoic acid synthase (phaC) gene from Chromobacterium violaceum[J]. Applied Environmental Microbiology, 1999, 65(8):3561-3565. [27] 吕俊, 于存. 一株高效溶磷伯克霍尔德菌的筛选鉴定及其对马尾松幼苗的促生作用[J]. 应用生态学报, 2020, 31(9):2923-2934. [28] Parke J L, Gurian-Sherman D. Diversity of the Burkholderia cepacia complex and implications for risk assessment of biological control strains[J]. Annual Review Phytopathology, 2001, 39(1):225-258. [29] Keel C, Schnider U, Maurfofer M, et al. Suppression of root diseases by Pseudomonas fluorescens CHA0:importance of the bacterial secondary metabolite 2,4-diacetylphloroglucinol[J]. Molecular Plant-Microbe Interactions, 1992, 5(1):4-13. [30] Loper J E, Henkels M D, Shaffer, B T, et al. Isolation and identification of rhizoxin analogs from Pseudomonas fluorescens Pf-5 by using a genomic mining strategy[J]. Applied Environmental Microbiology, 2008, 74(10):3085-3093. [31] Michelsen C F, Watrous J, Glaring M A, et al. Nonribosomal peptides, key biocontrol components for Pseudomonas fluorescens In5, isolated from a Greenlandic suppressive soil[J]. mBio, 2015, 6(2):e00079-15. [32] Zhao H, Liu Y P, Zhang L Q. In silico and genetic analyses of cyclic lipopeptide synthetic gene clusters in Pseudomonas spp. 11K1[J]. Frontiers in Microbiology, 2019, 10:544. [33] Taylor S D, Palmer M. The action mechanism of daptomycin[J]. Bioorganic and Medicinal Chemistry, 2016, 24(24):6253-6268. [34] Suvorova I A, Korostelev Y D, Gelfand M S. GntR family of bacterial transcription factors and their DNA binding motifs:structure, positioning and co-evolution[J]. PloS ONE, 2015, 10(7):e0132618. [35] Daddaoua A, Corrla-Lugo A, Ramos J L, et al. Identification of GntR as regulator of the glucose metabolism in Pseudomonas aeruginosa[J]. Environmental Microbiology, 2017, 19(9):3721-3733. [36] Yu Lingjun, Gao Wenyan, Li Shuxian, et al. GntR family regulator SCO6256 is involved in antibiotic production and conditionally regulates the transcription of myo-inositol catabolic genes in Streptomyces coelicolor A3(2)[J]. Microbiology (Reading, England), 2016, 162(3):537-551. [37] 刘晶, 李通, 刘增智, 等. 通过阻断调控基因ygrA挖掘海洋链霉菌OUC6819中抗MDR菌活性次级代谢产物[J]. 中国海洋药物, 2017, 36(5):16-22. |