Method for producing polyhydroxyalkanoate by fed-batch culture of bacillus bacteria in a medium containing date syrup
A method for producing a polyhydroxyalkanoate in a bacteria of a Bacillus species, the method comprising culturing the bacteria of the Bacillus species in a growth medium in the presence of a date syrup, said bacteria biosynthetically producing the polyhydroxyalkanoate intracellularly; and isolating the polyhydroxyalkanoate from the bacteria.
1. A method for producing a polyhydroxyalkanoate comprising:
fed-batch culturing Bacillus bacteria suspended in a culture medium containing date syrup,
separating the cultured bacteria from the growth medium,
lysing the separated cultured bacteria, and
isolating the polyhydroxyalkanoate;
wherein said Bacillus bacteria comprise a polynucleotide at least 95% identical to that described by GENBANK accession number HQ124332 (SEQ ID NO: 1).
2. The method of claim 1 , wherein the growth medium consists essentially of about 0.5 to 7% date syrup by volume based on a total volume of the growth medium, trace minerals and other non-sugar ingredients.
3. The method of claim 1 , wherein the date syrup comprises 1-90% v/v sugars, 1-10% v/v protein and 0.1-5% ash based on the total volume of the date syrup.
4. The method of claim 1 , wherein the date syrup comprises 15-20% by volume of fructose, 20-40% by volume of glucose, and 0.1 to 50% by volume of sucrose.
5. The method of claim 1 , wherein the growth medium contains no more than 10% v/v of tannins, citric acid or pectin; and wherein furfural, vanillin, levulinic acid, acetic acid, halogenated alkylacids, halogenated fatty acids, and halogenated sugars are not incorporated into it.
6. The method of claim 1 , wherein the growth medium further comprises 0.1%-5% v/v molasses or palm sugar, relative to the total volume of the growth medium.
7. The method of claim 1 , wherein the growth medium has a pH ranging from 6.9 to 7.4 and comprises 0.1 g/L-10 g/L of a nutrient broth other than date syrup containing 0.1 g/L-1 g/L of magnesium sulfate heptahydrate.
8. The method of claim 1 , wherein the growth medium has a pH ranging from 6.9 to 7.4 and comprises 0.1 g/L-10 g/L of a nutrient broth other than date syrup containing 0.1 g/L-1 g/L of magnesium sulfate heptahydrate, 0.05 g/L-1 g/L of zinc sulfate heptahydrate, 0.01-1.0 g/L of manganese chloride tetrahydrate, and 0.01 g/L-1.0 g/L copper sulfate tetrahydrate.
9. The method of claim 1 , wherein the culturing comprises growing the bacteria at a growth temperature of 25° C.-38° C. under mechanical agitation in a fed-batch process vessel.
10. The method of claim 1 , wherein the bacteria are forced to synthesize polyhydroxyalkanoate by culturing in a fed-batch process vessel for a period of 20 to 84 hours in a fed-batch phase in which the date syrup is added to the growth medium at a limiting level of 0.1%-5% v/v relative to a volume of the bacteria or at a limiting level of 5 to 50 g/L based on the volume of the growth medium.
11. The method of claim 1 , wherein the bacteria are forced to synthesize polyhydroxyalkanoate by culturing in a fed-batch process vessel for a period of 20 to 84 hours in a fed-batch phase in which the date syrup is added to the growth medium at a limiting level of 0.1%-5% v/v relative to a volume of the bacteria or at a limiting level of 5 to 50 g/L based on the volume of the growth medium; wherein the limiting level is administered by a pulse, a shot feeding, a linearly modulated feeding, an exponentially modulated feeding, or a constant feeding during fed-batch culturing.
12. The method of claim 1 , wherein the culturing further comprises reducing the growth temperature to an ambient temperature of 20° C.-24° C. after a fed-batch phase.
13. The method of claim 1 , wherein isolating the polyhydroxyalkanoate comprises recovering intracellular inclusion bodies and dispersing membranes surrounding the inclusion bodies to recover the polyhydroxyalkanoate.
14. The method of claim 1 , wherein isolating the polyhydroxyalkanoate comprises:
separating the bacteria from the growth media;
resuspending the bacteria in a detergent media, optionally containing lysozyme;
freezing the bacteria in the detergent media;
warming the bacteria in the detergent media to 30° C.-40° C. to lyse the bacteria;
sonicating the lysed bacteria in the detergent media optionally in the presence of a secondary detergent; and
separating the supernatant from the lysed bacteria.
15. The method of claim 14 , wherein the separating comprises centrifugation, settling, and/or filtration.
16. The method of claim 14 , wherein the detergent medium for sonicating the lysed bacteria further comprises at least one secondary detergent selected from the group consisting of polyethylene glycol sorbitan monolaurate, 4-(1,1,3,3-tetramethylbutyl)phenyl-polyethylene glycol, sodium dodecyl sulfate, 3-((3-cholamidopropyl) dimethylammonio)-1-propanesulfonate, and n-Octyl-β-D-thioglucopyranoside.
17. The method of claim 14 , wherein the detergent media further comprises at least One chaotropic agent selected from the group consisting of butanol, ethanol, guanidinium chloride, lithium perchlorate, lithium acetate, magnesium chloride, phenol, propanol, thiourea, and urea and a buffer that provides a pH of 5 to 8.
18. The method of claim 14 , further comprising sonicating after adding the secondary detergent.
19. The method of claim 14 , wherein the polyhydroxyalkanoate is a polyhydroxybutyrate.
20. The method of claim 14 , wherein the polyhydroxyalkanoate is a polyhydroxyvalerate.