Method for increasing yield of extracellular polysaccharide produced by submerged fermentation of long thread moss cells
An extracellular polysaccharide, deep fermentation technology, applied in the directions of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve problems such as no related literature reports on the yield of Nostoc polysaccharide, achieve high production efficiency, increase yield, Yield improvement effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0014] Embodiment 1: comparative example
[0015] The Nostocella cell species used in the present invention is isolated and preserved by Tianjin Key Laboratory of Industrial Microbiology (Chinese patent ZL031191101.0, inventors: Jia Shiru, Su Jianyu, Qiao Changsheng, date of authorization: March 8, 2006).
[0016] This invention separates and obtains the long-term preservation of Nostocchia cell species from the wild Nostocchis algae, carries out the suspension culture of Nostocys cells, adopts high-density culture technology, and adds the mixed nutrition mode of organic carbon source (Chinese patent 2006100113589.4, inventor: Jia Shiru Yu Haifeng, Su Jianyu, Lin Yongxian, published), using BG-11 medium supplemented with glucose, cultured for 7 days, the temperature was 24°C, the rotation speed was 140rpm, and the light intensity was 40-90μmol / m 2 ·s, the yield of polysaccharides of Nostocaria spp. was 2.25g / L.
Embodiment 2
[0018] The light reactor adopts the method of controlling light intensity and culture medium in stages, and the conditions such as temperature and rotation speed are the same as those in Comparative Example 1.
[0019] In the 4th day of the first stage of fermentation, nitrogenous BG-11 medium with 4g / L glucose was used, and the light intensity was controlled at 40~60μmol / m 2 s, on the fifth day of culture, feed nitrogen-free BG-11 medium with 2g / L sodium acetate and 3-3.5g / L glucose, adjust the pH above 9.0, and control the average light intensity of the liquid surface at 100-160μmol / m 2 ·s.
[0020] Using this step-by-step control strategy to produce polysaccharides from Nostoconia spp., the yield of polysaccharides obtained by ethanol precipitation was 3.5g / L.
Embodiment 3
[0022] The light reactor adopts the method of controlling light intensity and culture medium in stages, and the conditions such as temperature and rotation speed are the same as those in Comparative Example 1.
[0023] In the 4 days of the first stage of submerged fermentation, the aerobic BG-11 medium supplemented with 4g / L glucose was used, and the light intensity was controlled at 40-60μmol / m 2 s, harvest the cells on the 5th day of cultivation, all transfer to the nitrogen-free BG-11 medium that adds 2g / L sodium acetate and 4g / L glucose, adjust the pH of the medium above 9.0, and light intensity (average value of the liquid level) ) is controlled at 100~160μmol / m 2 ·s.
[0024] Using this step-by-step control strategy to produce the polysaccharides of Nostoconia spp., the yield of polysaccharides obtained by the two-stage fermentation broth was 4g / L by ethanol precipitation.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More