NifTAL Project, Department of Agronomy and Soil Science, University of Hawaii, Honolulu, Hawaii 96822.
Appl Environ Microbiol. 1985 Aug;50(2):398-405. doi: 10.1128/aem.50.2.398-405.1985.
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 degrees 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 degrees 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 degrees 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.
充分成长的各种快速和慢速生长根瘤菌的肉汤培养物在无菌掺入到聚丙烯袋中的灭菌泥炭(无菌方法)或与在托盘灭菌的泥炭(托盘方法)之前用各种稀释剂故意稀释。在无菌方法的析因实验中,使用来自五个国家的灭菌和辐照泥炭样本制备接种剂,用三种根瘤菌的水稀释培养物。当使用蒸馏水作为稀释剂时,与使用无菌方法时具有高营养状态的稀释剂相比,根瘤菌在泥炭中的繁殖和存活情况相似。在析因实验中,在 28°C 下储存 24 周后,每克接种剂的活菌数平均为 log 9.23(菌株 TAL 102)> log 8.92(菌株 TAL 82)> log 7.89(菌株 TAL 182)。来自阿根廷的泥炭对三种根瘤菌最优越,在储存期结束时每克的活菌数平均为 log 9.0。与用灭菌泥炭相比,用辐照泥炭生产的用稀释培养物制成的接种剂的质量明显(P = 0.05)更好,这是从析因实验中得出的结果。用托盘方法,在存在接种后污染物的情况下,用 1000 倍或更低倍数稀释的培养物中的根瘤菌在平板计数、膜滤免疫荧光和植物感染程序中繁殖和储存令人满意。在这两种方法中使用的所有根瘤菌菌株在 28°C 下储存时都会在接种剂中出现不同程度的种群减少。在 4°C 下储存时,两种方法产生的成熟接种剂中的快速和慢速生长根瘤菌的存活率显著(P <0.01)下降,而一些菌株的存活率在相同温度下显著(P <0.01)增加。用稀释培养物和灭菌泥炭生产的接种剂的植物有效性与用未稀释培养物和γ辐照泥炭生产的接种剂没有显著差异。