Method for reducing aberration rate of kelp germplasm parthenogenesis sporophytes
A technology of young sporophyte and female gametophyte, which is applied in the field of reducing the parthenogenetic deformity rate of female germplasm of kelp, and can solve problems such as environmental conditions not meeting the special requirements of parthenogenetic growth, high parthenogenous deformity rate, and missing chromosomes. Achieve good synchronization, shorten ovulation time, and high ovulation rate
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[0032] Embodiment 1: promote kelp germplasm to discharge ovum
[0033] 1) Prepare germplasm material for parthenogenetic development
[0034] The female germplasm filaments of kelp (Saccharina japonica) with dark brown color and no algae pollution were selected from the germplasm bank, and part of the germplasm was poured out for induction materials. Those used to induce germplasm were placed in 500ml sterile sea water.
[0035] 2) Pre-treatment for induction
[0036] The germplasm used for induction was placed in an induction incubator 24 hours before induction, the culture temperature was 15±1°C, the light source was a fluorescent tube, and the light was 1000lx, increasing by 500lx per hour until 6000±200lx.
[0037] 3) Ovulation induction treatment
[0038] The germplasm was crushed with a tissue grinder at 1500 rpm for 30 seconds, and repeated once. Then filter three times with a single-layer 500-mesh sieve to obtain filament fragments with a length of 3-6 cells.
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