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Mass Production of Spores of Lactic Acid-Producing Rhizopus oryzae NBRC 5384 on Agar Plate

机译:在琼脂平板上大量生产产乳酸米根霉NBRC 5384的孢子

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Mass production of sporangiospores (spores) of Rhizopus oryzae NBRC 5384 (identical to NRRL 395 and ATCC 9363) on potato-dextrose-agar medium was studied aiming at starting its L(+)-lactic acid fermentation directly from spore inoculation. Various parameters including harvest time, sowed spore density, size of agar plate, height of air space, and incubation mode of plate (agar-on-bottom or agar-on-top) were studied. Ordinarily used shallow Petri dishes were found out to be unsuitable for the full growth of R. oryzae sporangiophores. In a very wide range of the sowed spore density, the smaller it was, the greater the number of the harvested spores was. It was also interesting to find out that R. oryzae grown downward vertically with a deep air space in an agar-on-top mode gave larger amount of spores than in an agar-on-bottom mode at 30°C for 7-day cultivation. Scale-up of the agar plate culture from 26.4 to 292 cm~2 was studied, resulting in the proportional relationship between the number of the harvested spores/plate and the plate area in the deep Petri dishes. The number of plates of 50 cm in diameter needed for 100 m~3 industrial submerged fermentation started directly from 2 × 10~5 spores/mL inoculum size was estimated as about 6, from which it was inferred that such a fermentation would be feasible. Designing a 50 cm plate and a method of spreading and collecting the spores were suggested. Bioprocess technological significance of the "full-scale industrial submerged fermentation started directly from spore inoculation omitting pre-culture" has been discussed.
机译:研究了在马铃薯葡萄糖琼脂培养基上大量生产米根霉NBRC 5384(与NRRL 395和ATCC 9363相同)的孢子孢子(孢子)的目的,目的是直接从孢子接种开始其L(+)-乳酸发酵。研究了收获时间,播种孢子密度,琼脂平板大小,空气高度和平板的培养模式(底部琼脂或顶部琼脂)的各种参数。发现通常使用的浅培养皿不适合米曲霉孢子囊的完全生长。在播种的孢子密度的很大范围内,它越小,收获的孢子数量越多。还发现有趣的是,在30°C下进行7天培养时,在顶盖琼脂模式下在深空气空间中垂直向下生长的米曲霉产生的孢子数量要多于在30°C下的琼脂底模式。 。研究了琼脂平板培养物从26.4扩大至292 cm〜2的规模,得出了深培养皿中收获的孢子/平板数与平板面积之间的比例关系。 100 m〜3工业深层发酵所需的直径为50 cm的平板数直接从2×10〜5孢子/ mL接种物大小开始,估计约为6,由此推断这种发酵是可行的。建议设计一个50厘米的平板以及散布和收集孢子的方法。讨论了“直接从省略预培养的孢子接种开始的大规模工业深层发酵”的生物工艺技术意义。

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