首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Inoculant Production with Diluted Liquid Cultures of Rhizobium spp. and Autoclaved Peat: Evaluation of Diluents Rhizobium spp. Peats Sterility Requirements Storage and Plant Effectiveness
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Inoculant Production with Diluted Liquid Cultures of Rhizobium spp. and Autoclaved Peat: Evaluation of Diluents Rhizobium spp. Peats Sterility Requirements Storage and Plant Effectiveness

机译:用根瘤菌属稀释液体培养物生产孕育剂。和高压灭菌的泥炭:稀释剂根瘤菌泥炭无菌要求储存和植物有效性的评估

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摘要

Fully grown broth cultures of various fast- and slow-growing rhizobia were deliberately diluted with various diluents before their aseptic incorporation into autoclaved peat in polypropylene bags (aseptic method) or mixed with the peat autoclaved in trays (tray method). In a factorial experiment with the aseptic method, autoclaved and irradiated peat samples from five countries were used to prepare inoculants with water-diluted cultures of three Rhizobium spp. When distilled water was used as the diluent, the multiplication and survival of rhizobia in the peat was similar to that with diluents having a high nutrient status when the aseptic method was used. In the factorial experiment, the mean viable counts per gram of inoculant were log 9.23 (strain TAL 102) > log 8.92 (strain TAL 82) > log 7.89 (strain TAL 182) after 24 weeks of storage at 28°C. The peat from Argentina was the most superior for the three Rhizobium spp., with a mean viable count of log 9.0 per g at the end of the storage period. The quality of inoculants produced with diluted cultures was significantly (P = 0.05) better with irradiated than with autoclaved peat, as shown from the factorial experiment. With the tray method, rhizobia in cultures diluted 1,000-fold or less multiplied and stored satisfactorily in the presence of postinoculation contaminants, as determined by plate counts, membrane filter immunofluorescence, and plant infection procedures. All strains of rhizobia used in both the methods showed various degrees of population decline in the inoculants when stored at 28°C. Fast- and slow-growing rhizobia in matured inoculants produced by the two methods showed significant (P < 0.01) decline in viability when stored at 4°C, whereas the viability of some strains increased significantly (P < 0.01) at the same temperature. The plant effectiveness of inoculants produced with diluted cultures and autoclaved peat did not differ significantly from that of inoculants produced with undiluted cultures and gamma-irradiated peat.
机译:在将无菌包装掺入聚丙烯袋中高压灭菌的泥炭之前(无菌方法),有意将各种速生和缓慢生长的根瘤菌的完全生长的肉汤培养物用各种稀释剂稀释,或与在托盘中高压灭菌的泥炭混合(托盘方法)。在采用无菌方法的析因实验中,使用了来自五个国家的高压灭菌和辐照泥炭样品,以水稀释的三种根瘤菌属培养物制备接种物。当使用蒸馏水作为稀释剂时,泥炭中根瘤菌的繁殖和存活与使用无菌方法时营养水平高的稀释剂相似。在阶乘实验中,在28°C储存24周后,每克接种物的平均存活数为log 9.23(菌株TAL 102)> log 8.92(菌株TAL 82)> log 7.89(菌株TAL 182)。来自阿根廷的泥炭是三个根瘤菌属中最优质的,在储存期结束时,平均活菌数为每克9.0。如析因实验所示,用稀释培养物生产的孕育剂质量比用高压灭菌的泥炭辐照好(P = 0.05)。使用盘式方法,稀释度为1,000倍或更少的培养物中的根瘤菌在接种后污染物的存在下倍增并令人满意地储存,这由板数,膜滤器免疫荧光和植物感染程序确定。两种方法中使用的所有根瘤菌菌株在28°C储存时均显示接种物的不同程度的种群减少。两种方法生产的成熟接种物的根瘤菌快速生长和缓慢生长在4°C储存时均显示活力显着下降(P <0.01),而在相同温度下,某些菌株的活力显着提高(P <0.01)。用稀释培养物和高压灭菌的泥炭生产的孕育剂的植物效力与未稀释培养物和γ辐射泥炭生产的孕育剂的植物效力没有显着差异。

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