Application of lotus metallothionein gene MT2a in improving seed longevity and activity
A metallothionein and gene technology, applied in the field of molecular biology and biology, can solve problems such as the mechanism is not very clear, and achieve the effects of improving storage life and vitality, important economic benefits and application prospects, and reducing agricultural losses.
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Embodiment 1
[0032] Example 1: Lotus metallothionein gene MT2a Clone of
[0033] (1) Preparation of lotus seed hypocotyls: harvest the lotus seeds at the later stage of development and maturity, and strip the hypocotyls;
[0034] (2) Extraction of total RNA: Use Trizol product of Invitrogen to extract total RNA;
[0035] (3) cDNA library construction: use Clontech's SMART cDNA library construction kit to construct the library;
[0036] (4) EST sequencing: The obtained positive monoclonal bacterial liquid is a sequencing sample, and Shanghai Boya Biotechnology Company is entrusted to sequence the positive monoclonal after PCR verification with the 3730 sequencer;
[0037] (5) Homologous search: Use the BLAST tool to search for the homologous genes of the EST sequence in GenBank, and confirm that the gene obtained is the lotus metallothionein gene.
Embodiment 2
[0038] Example 2: Construction of plant expression vector
[0039] (1) Cloning of gene fragments: using the lotus cDNA library described in Example 1 as a template, cloned by PCR and added restriction sites Sma I and Sac PCR fragment of I. The PCR primers are as follows, and the underlined part is the restriction site.
[0040] Forward primer: SEQ ID NO: 3:
[0041] 5′-TCC CCCGGG AATGTCTTGCTGCGGAGGA-3′
[0042] Reverse primer: SEQ ID NO: 4:
[0043] 5′-CTG GAGCTC GCCCTC CTCTCATTTGCAG-3′
[0044] The PCR reaction system is: 2 μl lotus cDNA library, 6 μl dNTP (2.5 mM), 1.5 μl forward primer (10 μM), 1.5 μl reverse primer (10 μM), 5 μl 10*PCR buffer, 1 μl EX Taq enzyme (product of Takara), and finally add deionized water to make the total system 50 μl. The PCR reaction conditions are: 94°C for 3 minutes; then enter the following cycle: 94°C for 30 seconds, 58°C for 30 seconds, 72°C for 30 seconds, a total of 30 cycles; finally 72°C extension for 7 minutes;
[0045] (2) T vector conne...
Embodiment 3
[0050] Example 3: Genetic transformation of Arabidopsis
[0051] A pretreatment of Arabidopsis transformation
[0052] When the main moss grows to 5-6cm, cut off the entire inflorescence at the base of the inflorescence and remove its top advantage. After 1 week, 4-6 new side moss will grow in the axillary buds. After the side moss inflorescences form flower buds and partially bloom Or when 1-2 siliques are formed, they can be used for transformation, and the grown siliques must be cut off before transformation. The day before transformation, water the plants with sufficient water and cover them with a plastic bag to maintain a high humidity environment.
[0053] Two preparation of the dip medium
[0054] The composition of the dip medium used to soak the Arabidopsis flaccid is 1 / 2MS medium containing 5% sucrose, pH=5.8 (adjusted with KOH), and autoclaved. Add 0.02%-0.05% surface active agent Silwet L-77 or surface active agent soil temperature-20 when used, and the operation needs...
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