Scenedesmus sp. and use thereof
A technology of Scenedesmus, dry weight, applied in the field of microorganisms, can solve the problems of low processing capacity and performance, and achieve the effects of fast oil accumulation, high oil content and high utilization rate
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0037] Take a water sample from Dianchi Lake in Yunnan, add 1 / 3 of the volume of BG11 medium, and culture it for about 5 days at 25°C and a light intensity of 40μmol / m2.s. Take the water sample and observe it under a microscope to judge the water sample. main species present in . Adjust the cell concentration to about 1000 cells / ml, take 100 μl of water sample and spread it on the solid agar plate of BG11 medium, at 25°C, the light intensity is 40 μmol / m 2 After culturing for about 10 days under the condition of about .s, a single algae colony can be seen to grow. Use an inoculation loop or a sterile toothpick to pick a single algae colony and inoculate it in BG11 medium for culture. This process is repeated until a purely cultured algal strain is obtained, which is numbered "ENN34" in the present invention.
Embodiment 2
[0038] Example 2 Identification of algae species and their classification on the phylogenetic tree.
[0039] Identification of algae strains takes a combination of morphological identification and molecular identification.
[0040] 1. Morphological identification (see figure 1 ): The algae strain ENN34 isolated above was observed under a 1000-fold microscope. The cells were spherical, 6-10um in size, with perichrome, a pyrenoid, and asexual reproduction to produce spore-like spores. Initially identified as Scenedesmus.
[0041] 2. Molecular identification:
[0042] A, Amplification of 18S nucleotide sequences from isolated algae
[0043] Genomic DNA of ENN 34 algae cultured for 4 days was extracted by CTAB method. Take a certain amount of cells, add an appropriate amount of CTAB buffer after grinding, homogenate, add an equal volume of phenol:chloroform for extraction, an equal volume of isopropanol for precipitation, wash with 75% ethanol and dissolve in a certain volume ...
example 3
[0055] Indoor culture, oil accumulation and pigment analysis of example 3 ENN34 algae:
[0056]The green cells of Scenedesmus strain ENN 34 in the logarithmic growth phase were inoculated in the prepared BG11 medium (see Table 1 for the formula), so that the cell density reached an OD750 of 0.2-0.8. During the cultivation process, the light intensity is controlled at 50-500umol / m2.s. During the cultivation period, the pH value of the medium is adjusted between 7-9 by introducing a mixture of 1.5-2% carbon dioxide and air into the culture medium. During the period, the temperature is controlled within the range of 15-35°C. The reactor used for the cultivation was a column reactor with an inner diameter of 40 mm and a length of 600 mm. During the cultivation process, samples were taken regularly to determine the dry weight, and the results were shown in Figure 4 . On the 16th day of cultivation, when the color of the algae liquid turns red, the algae liquid is collected, and...
PUM

Abstract
Description
Claims
Application Information

- Generate Ideas
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com