Strain of antagonistic poplar colletotrichumgloeosporioides and application thereof
A technology of anthrax bacteria and anthracnose, applied in the field of microorganisms, can solve the problems of difficult chemical pesticide control and environmental pollution, and achieve the effect of easy cultivation and maintenance, and wide adaptability
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Embodiment 1
[0044] Example 1 Screening and identification of antagonistic bacteria Bacillus atrophaeus XW2
[0045] 1. Screening of antagonistic bacteria Bacillus atrophaeus XW2 against poplar anthracnose
[0046] The bacterial strain of the present invention is collected from healthy poplars in Datangshan Village, Changping District, Beijing.
[0047] 1A) Take 1.5g of freshly collected healthy poplar leaves, put them in a sterilized mortar filled with 10mL of sterile water, add a little sterilized quartz sand to grind evenly, and let it stand for 15min. Take 1mL of suspension and dilute sequentially with 10-fold serial dilution method to obtain 10 -3 、10 -4 、10 -5 Concentration gradient dilution, take 0.1mL from each concentration gradient suspension, spread it on the LB medium plate with a sterile applicator stick, use sterile water as the control, put it in an incubator and invert it at a constant temperature of 28°C after smearing evenly Culture; LB medium (1000mL): tryptone 10g, ...
Embodiment 2B
[0062] Determination of the utilization of different carbon sources and nitrogen sources by the Bacillus atrophaeus XW2 strain of embodiment 2
[0063] 1. Determination of the utilization of different carbon sources by Bacillus atrophaeus XW2 strain
[0064] 1A) Referring to the method in the "Common Bacteria System Identification Manual", use the carbon source basal medium (each 1000mL contains (NH 4 ) 2 SO 4 2.0g, NaH 2 PO 4 ·H 2 O0.5g, K 2 HPO 4 0.5g, MgSO 4 ·7H 2 O0.2g, CaCl 2 2H 2 (00.1g, pH7.0-7.2), adding different carbon sources respectively, the final concentration of carbon sources is generally 0.1% to 0.2% except for sugar alcohols which are 0.5% to 1%. carbon source basal medium;
[0065] 1B) Pick an activated Bacillus atrophaeus XW2 bacteria in 1 mL of sterile water and shake and mix to prepare a bacterial suspension;
[0066] 1C) Take 10uL of the bacterial suspension and inoculate them into 5mL test tubes containing carbon source basal medium contain...
Embodiment 3B
[0079] Determination of the culture characteristics of embodiment 3 Bacillus atrophaeus XW2 bacterial strain
[0080] 1. Determination of the optimal medium for the growth of Bacillus atrophaeus XW2 strain
[0081] 1A) Prepare medium
[0082] LB medium composition: tryptone 10g, yeast extract 5g, NaCl 10g, distilled water to adjust the total volume to 1000ml, pH7.0-7.2;
[0083] NB medium composition: peptone 10g, beef extract 3g, NaCl 5g, distilled water to adjust the total volume to 1000ml, pH7.0-7.2;
[0084] PDB medium composition: potato 200g, glucose 20g, distilled water to adjust the total volume to 1000ml, pH7.0-7.2;
[0085] Gaoshi No. 1 medium composition: soluble starch 20g, KNO 3 1g, NaCl0.5g, K 2 HPO 4 0.5g, MgSO 4 ·7H 2 O0.5g, FeSO 4 ·7H 2 O0.01g, distilled water to adjust the total volume is 1000ml, pH7.0-7.2;
[0086] King B2 medium composition: peptone 20g, MgSO 4 ·7H 2 O1.5g, glycerol 10mL, K 2 HPO 4 1.5g, distilled water to adjust the total vol...
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