US20150225759A1

US20150225759A1 - Sophorolipids as protein inducers and inhibitors in fermentation medium

Info

Publication number: US20150225759A1
Application number: US14/690,837
Authority: US
Inventors: Richard A. Gross; Vishal Shah; Frantisek Nerud; Datta Madamwars
Original assignee: SyntheZyme LLC
Current assignee: SyntheZyme LLC
Priority date: 2004-12-22
Filing date: 2015-04-20
Publication date: 2015-08-13
Also published as: US9012194B2; WO2007073371A1; US20080076165A1; EP1963518A4; EP1963518A1; CA2600442A1

Abstract

A method for producing sophorolipids having protein inducer and/or repressor activities having the steps of synthesizing the sophorolipid by fermentation of Candida bombicola in a fermentation media to form a natural mixture of lactonic sophorolipids and non-lactonic sophorolipids and then utilizing the natural mixture as a protein inducing agent, utilizing the natural mixture as a protein repressing agent, and/or utilizing the natural mixture as a combined protein induction/repressor agent. An application of the sophorolipid compound produced according to the method as a microbial media component.

Description

STATEMENT OF RELATED APPLICATIONS

This patent application is a divisional of U.S. patent application Ser. No. 11/722,356 having a filing date of 11 Dec. 2007, which is the US National Phase application of International Application No. PCT/US2005/046457 having an International Filing Date of 22 Dec. 2005, which is based on and claims priority on U.S. Provisional Patent Application No. 60/638,747 having a filing date of 22 Dec. 2004.

BACKGROUND OF THE INVENTION

1. Technical Field
The present invention in general relates to the field of uses for sophorolipids and more specifically to the field of protein inducers and as a media component. The invention is directed to developing low cost inducers/repressors for protein production.

2. Prior Art

For production of proteins on a larger scale, a need exists for cheap and well defined molecules to act as inducers of the protein of interest and also as a repressor for unwanted enzymes. This aids in higher yields, decreasing the purification costs and enhancing the profits. Sophorose has been shown to be a good inducer of cellulase protein. See Hrmova, M., Petrakova, E., Biely, P., Journal of General Microbiology 137, 541-547 (1991). However, the cost of the molecule makes it impractical to be used at commercial level.
Sophorolipids are microbial extracellular glycolipids produced by resting cells of Candida bombicola. The chemical composition of sophorolipid is constituted by a disaccharide sugar viz. sophorose and a fatty acid or an ester group. Candida bombicola produces the sophorolipids as a mixture of macroloctones and free acid structures that are acetylated to various extents at the primary hydroxyl sophorose ring positions (FIG. 1). See Bisht, K. S. et al., J. Org. Chem., vol. 64, pp. 780-789 (1999).
It is to the development of sophorolipids for production and industrial purposes, and other purposes, that the present invention is directed.

BRIEF SUMMARY OF THE INVENTION

A natural mixture of sophorolipids was synthesized by fermentation of Candida bombicola. When B. subtilis was grown in presence of sophorolipids, increased production of amylase was observed. When Pleurotus ostreatus 473 strain, which produces both laccase and manganese peroxidase, was grown in the presence of sophorolipids, increased production of laccase was observed while the production of manganese peroxidase decreased.
Thus, the applications of sophorolipids in the fields of industry and basic sciences would have tremendous advantages in higher production or inhibition rates of proteins. Further, while sophorolipids can find applications in diversified fields, the present invention indicates that sophorolipids could be used as protein inducers and repressors.
These features, and other features and advantages of the present invention, will become more apparent to those of ordinary skill in the relevant art when the following detailed description of the preferred embodiments is read in conjunction with the appended drawing.

BRIEF DESCRIPTION OF THE FIGURE

FIG. 1 are representative structures of sophorolipids produced by Candida bombicola, with FIG. 1A showing lactonic sophorolipid and FIG. 1B showing open ring sophorolipid.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

1. Sophorolipid Fermentation
Sophorolipids were synthesized by fermentation of Candida bombicola. The fermentation media was composed of glucose 100 g, yeast extract 10 g, urea 1 g and oleic acid 40 g in 1000 ml of water. After 7 days of fermentation, sophorolipid was extracted thrice using ethyl acetate. The extracts were pooled and the solvent then was removed. The obtained product was therein washed with hexane to remove the residual fatty acids. This was “natural” sophorolipid. The sophorolipid was dried in a vacuum desiccator.
2. Study of Amylase Protein Induction
Bacillus subtilis strain was used to study the effect of sophorolipid on amylase induction. Culture was grown on Peptone: 5 gm/L, Beef extract: 3 gm/L and Starch: 2 gm/L. A single colony of Bacillus subtilis was inoculated in 10 ml medium and was allowed to grow for 12 hours. After the culture reached to the log phase, 1 ml of the same was inoculated in 100 ml of the medium. Control experiments having no sophorolipids also were conducted, whereas the experimental set has 1 mM of sophorolipid prepared in DMSO.
After 48 hours a sample was withdrawn, centrifuged at 8000 rpm for 20 minutes, and amylase activity determined using standard methods.
3. Study of Laccase Protein Induction and Manganese Peroxide Repression
Pleurotus ostreatus 473 was used to study the effect of sophorolipids on Laccase/Manganese peroxidase production. Culture was cultivated in agar medium containing 5 g/L cellulose, 1 g/L KH₂PO₄, 0.5 g/L MgSO₄.7H₂O, 0.2 g/L ammonium tartrate, 0.2 g/L NaH₂PO₄, 50 mg/L CaCl₂, 50 mg/L, FeSO₄.7H₂O, 10 mg/L CuSO₄. 5H₂O, 5 mg/L ZnSO₄.7H₂O, 5 mg/L MnSO₄.4H₂O and 25 g/L agar. pH of the medium was 6.0. For enzyme production studies, flasks with 20 mL of the above media (without agar) were inoculated with two wort agar plugs (2° Balling, 10 mm diameter), cut from the actively growing part of a colony on a Petri dish, and incubated at 27° C. for 14 days. After 14 days a sample was withdrawn, centrifuged at 8000 rpm for 20 minutes and laccase and MnP activity determined using standard methods.

RESULTS AND DISCUSSION

As shown in Table 1, upon growing B. subtilis in the presence of sophorolipid, an increase of 39% amylase protein production observed. Growing Pleurotus ostreatus 473 in the presence of 1 mM sophorolipid natural mixture resulted in 4.5 times increase in laccase protein whereas there was a decrease of 25% in the production of manganese peroxide protein. This shows that the sophorolipid natural mixture has the ability to act as an inducer for some proteins and the ability to act as a repressor for others.
The invention will find its place in industries that produce protein products such as enzymes through microbial fermentation. Also, microbial media that has sophorolipids as a component can be sold for protein induction studies.
Sophorolipids will be administered in the fermentation medium as either fine powder or in the form of solutions prepared in DMSO, alkaline sucrose solution, chloroform, methanol or ethyl acetate.

TABLE 1

% Increase/decrease of enzyme production

	Enzyme	% values

	Laccase
	Control	100
	Sophorolipid Induced	453
	Manganese peroxidase
	Control	100
	Sophorolipid Induced	73
	Amylase
	Control	100
	Sophorolipid induced	139

The foregoing detailed descriptions of the preferred embodiments and the appended FIGURE have been presented only for illustrative and descriptive purposes and are not intended to be exhaustive or to limit the scope and spirit of the invention. The embodiments were selected and described to best explain the principles of the invention and its practical applications. One skilled in the art will recognize that many variations can be made to the invention disclosed in this specification without departing from the scope and spirit of the invention.

Claims

What is claimed is:

1. A method for producing sophorolipids having protein inducer and/or repressor activities comprising the steps of:

a) synthesizing the sophorolipid by fermentation of Candida bombicola in a fermentation medium to form a natural mixture of lactonic sophorolipids and non-lactonic sophorolipids; and

b) utilizing the natural mixture as a protein inducing agent.

2. The method according to claim 1, wherein the fermentation medium comprises glucose, yeast extract, urea, and oleic acid in water.

3. The method according to claim 2, further comprising, after a period of fermentation, extracting the sophorolipid using ethyl acetate as a solvent.

4. The method according to claim 3, further comprising removing the solvent and washing the obtained product with hexane to remove residual fatty acids, resulting in the natural mixture of sophorolipids.

5. The method according to claim 4, further comprising drying the natural mixture of sophorolipids.

6. The method according to claim 1, further comprising adding an effective amount of the natural mixture of sophorolipids as a protein inducing agent to a microbial culture medium.

7. The method according to claim 6, wherein the protein is selected from the group consisting of amylase, laccase, and manganese peroxidase, and combinations thereof.

8. A method for producing sophorolipids having protein inducer and/or repressor activities comprising the steps of:

b) utilizing the natural mixture as a protein repressing agent.

9. The method according to claim 8, wherein the fermentation medium comprises glucose, yeast extract, urea, and oleic acid in water.

10. The method according to claim 9, further comprising, after a period of fermentation, extracting the sophorolipid using ethyl acetate as a solvent.

11. The method according to claim 10, further comprising removing the solvent and washing the obtained product with hexane to remove residual fatty acids, resulting in the natural mixture of sophorolipids.

12. The method according to claim 11, further comprising drying the natural mixture of sophorolipids.

13. The method according to claim 8, further comprising adding an effective amount of the natural mixture of sophorolipids as a protein repressing agent to a microbial culture medium.

14. The method according to claim 13, wherein the protein is selected from the group consisting of amylase, laccase, and manganese peroxidase, and combinations thereof.

15. A method for producing sophorolipids having protein inducer and/or repressor activities comprising the steps of:

b) utilizing the natural mixture as a combined protein induction/repressor agent.

16. The method according to claim 15, wherein the fermentation medium comprises glucose, yeast extract, urea, and oleic acid in water.

17. The method according to claim 16, further comprising, after a period of fermentation, extracting the sophorolipid using ethyl acetate as a solvent.

18. The method according to claim 17, further comprising removing the solvent and washing the obtained product with hexane to remove residual fatty acids, resulting in the natural mixture of sophorolipids.

19. The method according to claim 18, further comprising drying the natural mixture of sophorolipids.

20. The method according to claim 15, further comprising adding an effective amount of the natural mixture of sophorolipids as a protein inducing and repressing agent to a microbial culture medium.

21. The method according to claim 20, wherein the protein is selected from the group consisting of amylase, laccase, and manganese peroxidase, and combinations thereof.