Biology Department, Utah State University, Logan, Utah 84322-5305.
Appl Environ Microbiol. 1990 Nov;56(11):3576-82. doi: 10.1128/aem.56.11.3576-3582.1990.
Root-colonizing, saprophytic fluorescent pseudomonads of the Pseudomonas putida-P. fluorescens group express similar levels of catalase and superoxide dismutase activities during growth on a sucrose- and amino acid-rich medium. Increased specific activities of catalase but not superoxide dismutase were observed during growth of these bacteria on components washed from root surfaces. The specific activities of both enzymes were also regulated during contact of these bacteria with intact bean roots. Increased superoxide dismutase and decreased catalase activities were observed rapidly, by 10 min upon inoculation of cells onto intact bean roots. Catalase specific activity increased with time to peak at 12 h before declining. By 48 h, the cells displayed this low catalase but maintained high superoxide dismutase specific activities. Catalase with a low specific activity and a high superoxide dismutase activity also were present in extracts of cells obtained from 7-day-old roots colonized from inoculum applied to seed. This specific activity of superoxide dismutase of root-contacted cells was about fourfold-higher in comparison to cells grown on rich medium, whereas the specific activity for catalase was reduced about fivefold. A single catalase isozyme, isozyme A, and one isozyme of superoxide dismutase, isozyme 1, were detected during growth of the bacteria on root surface components and during exposure of cells to intact bean roots for 1 h. An additional catalase, isozyme B, was detected from bacteria after exposure to the intact bean roots for 12 h. Catalase isozyme A and superoxide dismutase isozyme 1 were located in the cytoplasm and catalase band B was located in the membrane of P. putida.
生存在植物根系的、具有根际定殖能力的、腐生的荧光假单胞菌(Pseudomonas putida-P. fluorescens group)在富含蔗糖和氨基酸的培养基中生长时,其过氧化氢酶和超氧化物歧化酶的活性表达水平相似。当这些细菌在从根表面冲洗下来的成分上生长时,观察到过氧化氢酶的比活增加,而超氧化物歧化酶的比活没有增加。在这些细菌与完整的豆根接触时,两种酶的比活也受到调节。当细胞接种到完整的豆根上时,迅速观察到超氧化物歧化酶活性增加,而过氧化氢酶活性降低,接种后 10 分钟即可观察到。过氧化氢酶的比活随着时间的推移而增加,在 12 小时时达到峰值,然后下降。到 48 小时时,细胞表现出这种低过氧化氢酶活性,但保持高超氧化物歧化酶比活。在接种到种子上的接种物中获得的 7 天龄根定殖细胞的提取物中,也存在具有低比活的过氧化氢酶和高比活的超氧化物歧化酶的细胞。与在丰富培养基中生长的细胞相比,接触根的细胞的超氧化物歧化酶的比活约高四倍,而过氧化氢酶的比活降低约五倍。在细菌生长在根表面成分上以及暴露于完整的豆根 1 小时期间,检测到一种单一的过氧化氢酶同工酶,同工酶 A,和一种超氧化物歧化酶同工酶 1。在将细菌暴露于完整的豆根 12 小时后,检测到另一种过氧化氢酶同工酶 B。过氧化氢酶同工酶 A 和超氧化物歧化酶同工酶 1 位于细胞质中,而过氧化氢酶同工酶 B 位于 P. putida 的膜中。