Method for promoting rapid development of gametophytes of chelmydomonas palustris
A technology of gametophyte and Cheschiella, which is applied in the field of promoting the rapid development of Chessia pachyphyllum gametophytes, can solve the problems of reduced yield at harvest time, asynchronous development of male and female, and long development time, so as to reduce the time required for seedling cultivation and promote synchronization Growth, the effect of accelerating the development process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0022] Embodiment 1: optimize nitrogen source
[0023] Take an appropriate amount of the female and male gametophytes of Chrysophylla pachyphyllum, break them up for 5 minutes with a micro-submersible pump, and then filter them with a 300-mesh sieve to obtain a gametophyte cell segment with 2 to 5 cells as the main part. The female and male gametophytes were mixed at a mass ratio of 2:1, cultured in a Petri dish, at a temperature of 10°C, under white light, and an illumination intensity of 30 μmol photons / (m 2 s), photoperiod 20L: 4D, culture medium added effective N10mg / L, KH 2 PO 4 -P 1mg / L and FeC 6 h 5 o 7 - Sterilized seawater with Fe 0.5mg / L (sterilized by boiling to reduce the pollution of diatoms, etc.), and NaNO as nitrogen source 3 , CO(NH 2 ) 2 , NH 4 NO 3 , NH 4 Cl and NH 4 HCO 3 During the cultivation process, the culture medium was changed every 3 days. At the same time, the growth and development of the gametophytes were observed under the microscope...
Embodiment 2
[0030] Example 2: Optimizing Light Quality
[0031] Take an appropriate amount of female and male gametophytes of Chrysophylla pachyphyllum, break them up for 5 minutes with a micro-submersible pump, and then filter them with a 300-mesh sieve to obtain gametophytic cell segments with 2 to 5 cells as the main part. , and male gametophytes were mixed at a mass ratio of 2:1 and cultured in a petri dish at a temperature of 10°C and a light intensity of 30 μmol photons / (m 2 s), photoperiod 20L: 4D, the culture medium is added effective NaNO 3 -N 10mg / L, KH 2 PO 4 -P1mg / L and FeC 6 h 5 o 7- Fe 0.5mg / L sterilized seawater (sterilized by boiling), using different wavelengths of visible light (white light, blue light, red light), changing the culture medium every 3 days during the culture process, and at the same time under the microscope Observe the growth and development status of gametophytes, observe and take pictures, randomly observe 10 100×fields of view in each petri dish...
Embodiment 3
[0037] Example 3: Optimizing Fe Concentration
[0038] Take an appropriate amount of the female and male gametophytes of Chrysophylla pachyphyllum, break them up for 5 minutes with a micro-submersible pump, and then filter them with a 300-mesh sieve to obtain a gametophyte cell segment with 2 to 5 cells as the main part. Female and male gametophytes were mixed at a mass ratio of 2:1 and cultured in a Petri dish at a temperature of 10°C under white light with a light intensity of 30 μmol photons / (m 2 s), photoperiod 20L: 4D, the culture medium is added effective NaNO 3 -N10mg / L, KH 2 PO 4 -P1mg / L and FeC 6 h 5 o 7 - Fe sterilized seawater (sterilized by boiling), the amount of Fe added is set to 5 gradients, respectively 0.05mg / L, 0.1mg / L, 0.5mg / L, 1mg / L, 2mg / L, each There were 3 replicates in each group, and the culture medium was changed every 3 days during the culture process. At the same time, the growth and development of gametophytes were observed under a microscope...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com