Buell C R, Anderson A J
Department of Biology, Utah State University, Logan 84322-5305.
Mol Plant Microbe Interact. 1993 May-Jun;6(3):331-40. doi: 10.1094/mpmi-6-331.
In vitro agglutinability by Pseudomonas putida, isolate Corvallis, with a plant root surface agglutinin is correlated with rapid adhesion of cells of the fluorescent pseudomonad to bean (Phaseolus vulgaris) root surfaces. Agglutinability in P. putida cells is regulated by nutrient status as well as growth phase. Cells grown in three different nutrient complex media are agglutinable at early and mid-late logarithmic phase but become nonagglutinable at stationary phase. Cells grown in a minimal medium are weakly agglutinable, but the addition of lysine, aspartic acid, or histidine increases agglutinability. Cells in the same minimal medium supplemented with bean root surface components grow in a highly agglutinated state. Previous data indicate both agglutination and rapid adhesion to roots by P. putida Corvallis involves the aggA locus, which contains two putative open reading frames (ORF), ORF-AGG1 and ORFAGG2, on complementary strands. Sequence and deletion analyses suggest ORFAGG1 is the most probable ORF responsible for agglutination and adhesion. Chimeric fusion of an Escherichia coli lac promoter with ORFAGG1, but not with ORFAGG2, complemented agglutinability of an aggA::Tn5 P. putida Agg mutant, providing further evidence that ORFAGG1, not ORFAGG2, is responsible for agglutination. Heterologous expression of ORFAGG1 yields a 50-kDa precursor and a 48-kDa mature periplasmic protein. Fusions of ORFAGG1 and ORFAGG2 to the reporter gene, xylE, and detection of the reporter enzyme, catechol-2,3-oxygenase reveal an active promoter in the 5' noncoding region of ORFAGG1. The ORFAGG1 promoter is active during growth of the cells in liquid culture and is regulated by growth medium. Greatest activity of the catechol-2,3-oxygenase is observed in stationary phase when the cells are nonagglutinable. Expression of the ORFAGG1 promoter is detected in P. putida cells extracted from the root surface of bean at 48 and 72 hr after inoculation.
恶臭假单胞菌科瓦利斯分离株与植物根表面凝集素的体外凝集能力,与荧光假单胞菌细胞快速黏附到菜豆(Phaseolus vulgaris)根表面相关。恶臭假单胞菌细胞的凝集能力受营养状况以及生长阶段的调控。在三种不同的营养复合培养基中生长的细胞,在对数生长早期和中后期具有凝集能力,但在稳定期变为不可凝集。在基本培养基中生长的细胞凝集能力较弱,但添加赖氨酸、天冬氨酸或组氨酸会增加凝集能力。在添加了菜豆根表面成分的相同基本培养基中生长的细胞处于高度凝集状态。先前的数据表明,恶臭假单胞菌科瓦利斯的凝集和对根的快速黏附都涉及aggA基因座,该基因座在互补链上包含两个推定的开放阅读框(ORF),即ORF-AGG1和ORFAGG2。序列和缺失分析表明,ORFAGG1最有可能是负责凝集和黏附的ORF。大肠杆菌lac启动子与ORFAGG1而非ORFAGG2的嵌合融合,补充了aggA::Tn5恶臭假单胞菌Agg突变体的凝集能力,进一步证明负责凝集的是ORFAGG1而非ORFAGG2。ORFAGG1的异源表达产生一个50 kDa的前体和一个48 kDa的成熟周质蛋白。ORFAGG1和ORFAGG2与报告基因xylE的融合以及报告酶儿茶酚-2,3-加氧酶的检测,揭示了ORFAGG1 5'非编码区的一个活性启动子。ORFAGG1启动子在液体培养中的细胞生长期间具有活性,并受生长培养基调控。当细胞不可凝集时,在稳定期观察到儿茶酚-2,3-加氧酶的最大活性。在接种后48小时和72小时从菜豆根表面提取的恶臭假单胞菌细胞中检测到ORFAGG1启动子的表达。