Method for effectively screening out chlamydomonas hydrogen desorption mutant
A technology of mutants and Chlamydomonas, applied in the field of screening Chlamydomonas hydrogen-releasing mutants, can solve problems such as unclear mechanisms and regulation methods, ineffective genetic modification, and ineffective conversion of light energy to hydrogen. Achieve the effect of reducing workload and improving efficiency
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[0021] 1. Materials
[0022] 1. Plant material: Chlamydomonas reinhardtii (Chlamydomonas reinhardtii), algae species CC425 (arginine-deficient, Arg-) from Duke University algae library Chlamydomonas reinhardtii (Chlamy center, http: / / www.chlamy.org / ) were purchased; other mutants were obtained by our laboratory using T-DNA random insertion method.
[0023] 2. Plasmid: pJD67 plasmid was purchased from Duke University Chlamydomonas Center (Chlamy center, http: / / www.chlamy.org / ); The pJD67 plasmid is transformed from the commercialized pBluscript SK plasmid, with a full length of 11284bp, containing the gene of spermylsuccinate lyase and the gene of ampicillin resistance. When transforming algal strains, linearize with KpnI to improve the transformation efficiency. The sequence of pJD67 is sequence 1.
[0024] 3. Medium
[0025] 1) Normal TAP medium: NH 4 C1 0.4g / L; MgSO 4 ·7H 2 O 0.1g / L; CaCl 2 2H 2 O 0.05g / L; K 2 HPO 4 0.108g / L; KH 2 PO 4 0.056g / L; Trisbase 2.42...
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