Natural composition based on Chilean monofloral honey extract from native vegetable species for bacterial infection control in vegetables at all
AssigneesPontificia Universidad Catolica De Chile, Fundación Copec Universidad Católica
InventorGloria Montenegro Rizzardini
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Abstract
Natural composition for controlling bacterial infections in potatoes, lettuce, vegetables, cores and flowers in general comprising extracts from monofloral honey flavonoids and/or phenols that act independently as controller of various bacterial infections.
Claims7
An extract comprising flavonoids and/or phenols from monofloral ulmo honey (Eucryphia cordifolia), said extract comprising gallic acid in the amount of 0.236±0.005 μg/ml, coumaric acid in the amount of 0.221±0.005 μg/ml, pherulic acid in the amount of 0.235±0.005 μg/ml, salicylic acid in the amount of 0.435±0.005 μg/ml, naringenin in the amount of 0.456±0.005 μg/ml and kaempherol in the amount of 0.174±0.005 μg/ml, with a pH:
- 4.9 to 5.5, wherein said extract is prepared by a process comprising:
- a) weighing a quantity of honey;
- b) diluting said honey in distilled water acidified with HCI (pH=2) to form a solution;
- c) putting the solution in a volumetric flask and filling the flask up with additional acid water;
- d) filtering said solution obtained in step c) and passing it through a column of cationic exchange at a constant dropping speed for phenolic compounds to be retained in said column;
- e) cleaning said column with acid water and discarding the acid water that passes through the column;
- f) cleaning said column a second time with neutral distilled water and discarding the neutral distilled water that passes through the column;
- g) cleaning for a third time with pure methanol to elute the phenolic compounds from the column, gathering methanol elute, and rotoevaporating the methanol elute to vacuum dryness at a temperature of 45° C., in order to eliminate the methanol and concentrate the obtained phenolic compounds to form a residue in a rotoevaporator;
- h) re-suspending the residue in distilled water to form a suspension;
- i) extracting the suspension 3 times with diethyl ether to form a diethyl ether extraction solution;
- j) concentrating said diethyl ether extraction solution to dryness in a rotoevaporator to form a second residue;
- k) re-suspending the second residue in sterilized distilled water;
- l) filtering the resuspended residue through a nitrocellulose syringe filter of 20 μm and storing the filtered residue at −20° C.
Dependencies are inferred from the claim text.