Pseudoalteromonas fish killing and application thereof in aquaculture
A pseudoalteromonas and aquaculture technology, applied in the field of microorganisms, can solve problems such as difficulty in antagonizing pathogenic bacteria and immune function and promoting intestinal function, difficult and efficient application of bacterial disease technology, and few application technology reports, etc. Intestinal function, length increase, the effect of length increase
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Embodiment 1
[0049] Effect of Pseudoalteromonas piscicida 2013082515 on shrimp culture
[0050] 1. Material method
[0051] 1.1 Preparation of Pseudoalteromonas piscicida 2013082515 preparation
[0052] Take the 2013082515 strain of Pseudoalteromonas piscicida preserved at -80°C, streak it on 2216E solid medium, culture it at 28°C for 24 hours to obtain a single colony, and inoculate a single colony into the seed culture solution of Pseudoalteromonas piscicida In 28°C shake flask culture for 24 hours to obtain the seed liquid, then inoculate the seed liquid in the fermentation medium of Pseudoalteromonas ichthicida for 24 hours to carry out aerobic fermentation, the temperature is controlled at 28°C; when the OD600 value of the fermentation liquid reaches From 1.5 to 1.7 hours, the fermentation was terminated, and the fermentation broth was obtained, and the strain concentration of the fermentation broth was determined by plate counting.
[0053] The 16S rDNA base sequence of Pseudoalter...
Embodiment 2
[0090] Effect of Pseudoalteromonas piscicida 2013082515 on the culture of flounder
[0091] 1. Material method
[0092] 1.1 Preparation of Pseudoalteromonas piscicida 2013082515 preparation
[0093] Take the 2013082515 strain of Pseudoalteromonas piscicida preserved at -80°C, streak it on 2216E solid medium, culture it at 28°C for 24 hours to obtain a single colony, and inoculate a single colony into the seed culture solution of Pseudoalteromonas piscicida In 28°C shake flask culture for 24 hours to obtain the seed liquid, then inoculate the seed liquid in the fermentation medium of Pseudoalteromonas ichthicida for 24 hours to carry out aerobic fermentation, the temperature is controlled at 28°C; when the OD600 value of the fermentation liquid reaches From 1.5 to 1.7 hours, the fermentation was terminated, and the fermentation broth was obtained, and the strain concentration of the fermentation broth was determined by plate counting.
[0094] 1.2 Experimental flounder
[00...
Embodiment 3
[0131] Effect of Pseudoalteromonas piscicida 2013082515 on the breeding of bay scallops
[0132] 1. Material method
[0133] 1.1 Preparation of Pseudoalteromonas piscicida 2013082515 preparation
[0134] Take the 2013082515 strain of Pseudoalteromonas piscicida preserved at -80°C, streak it on 2216E solid medium, culture it at 28°C for 24 hours to obtain a single colony, and inoculate a single colony into the seed culture solution of Pseudoalteromonas piscicida In 28°C shake flask culture for 24 hours to obtain the seed liquid, then inoculate the seed liquid in the fermentation medium of Pseudoalteromonas ichthicida for 24 hours to carry out aerobic fermentation, the temperature is controlled at 28°C; when the OD600 value of the fermentation liquid reaches From 1.5 to 1.7 hours, the fermentation was terminated, and the fermentation broth was obtained, and the strain concentration of the fermentation broth was determined by plate counting.
[0135] 1.2 Bay scallop larvae used...
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