Modification of bacterial profile of tobacco

US9155334B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9155334-B2
Application numberUS-201313857677-A
CountryUS
Kind codeB2
Filing dateApr 5, 2013
Priority dateApr 5, 2013
Publication dateOct 13, 2015
Grant dateOct 13, 2015

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A method of modifying the content of certain bacteria in uncured tobacco material is provided, the method including contacting an uncured tobacco material with a treatment solution, wherein the treatment solution is selected from the group consisting of: (i) a solution comprising salt, sugar, or a combination thereof; (ii) a solution comprising one or more enzymes; and (iii) a solution comprising one or more probiotics, wherein said contacting provides a treated tobacco material having a reduced total bacterial content following harvest. In certain embodiments, the treated tobacco material is subsequently cured, and can optionally be fermented. Smoking articles and smokeless tobacco products including such treated tobacco materials are also provided.

First claim

Opening claim text (preview).

What is claimed: 1. A method of modifying the bacterial content of a tobacco material, comprising contacting an unharvested tobacco material less than about 24 hours before harvest with a treatment solution, wherein the treatment solution is selected from the group consisting of: (i) a solution comprising salt, sugar, or a combination thereof, wherein the salt is selected from the group consisting of NaCl, CaCl 2 , MgCl 2 , KCl, and combinations thereof; (ii) a solution comprising one or more enzymes; and (iii) a solution comprising one or more probiotic Lactobacillus bacteria, wherein said contacting provides a treated tobacco material having a reduced total bacterial content following harvest. 2. The method of claim 1 , wherein the unharvested tobacco material is selected from the group consisting of a tobacco seed, a tobacco seedling, an immature live plant, a mature live plant, or a portion thereof. 3. The method of claim 1 , wherein the total bacterial content of the treated tobacco material is reduced by at least about 50% in number following harvest. 4. The method of claim 1 , wherein the total bacterial content of the treated tobacco material is reduced by at least about 80% in number following harvest. 5. The method of claim 1 , wherein the total bacterial content of the tobacco material comprises Gram-negative bacteria and wherein the Gram-negative bacterial content of the treated tobacco material is reduced by at least about 50% in number following harvest. 6. The method of claim 1 , wherein the total bacterial content of the tobacco material comprises bacteria of the Lactobacillus genus, and wherein the Lactobacillus bacterial content of the treated tobacco material is increased following harvest. 7. The method of claim 1 , wherein the treatment solution comprises NaCl. 8. The method of claim 1 , wherein the treatment solution has a concentration of salt, sugar, or a combination thereof of between about 1 and about 4 percent by weight. 9. The method of claim 1 , wherein the treatment solution comprises Lactobacillus helveticus. 10. The method of claim 1 , wherein the treatment solution has a concentration of probiotic bacteria of between about 1×10 5 colony forming units/mL and about 1×10 10 colony forming units/mL. 11. The method of claim 1 , wherein the treatment solution has a concentration of enzyme of between about 10 AU and about 50,000 AU per plant. 12. The method of claim 1 , wherein the treatment solution further comprises a surfactant. 13. The method of claim 1 , further comprising curing the treated tobacco material to give a treated, cured tobacco material. 14. The method of claim 13 , wherein the tobacco-specific nitrosamine content of the treated, cured tobacco material is reduced relative to an untreated, cured tobacco material. 15. The method of claim 13 , further comprising subjecting the treated, cured tobacco material to fermentation, wherein the fermentation is completed in less time than that required for fermentation of untreated, cured tobacco material. 16. The method of claim 13 , further comprising: processing the treated, cured tobacco material to provide a processed tobacco material in a form suitable for incorporation in a tobacco product; and incorporating the processed tobacco material into a smokeless tobacco product or a smoking article. 17. The method of claim 16 , wherein the processed tobacco material is in the form of cut filler. 18. The method of claim 16 , wherein the processed tobacco material is in the form of a tobacco blend. 19. The method of claim 16 , wherein the smoking article, upon smoking, is characterized by a TSNA content of mainstream smoke that is reduced relative to an untreated control smoking article. 20. The method of claim 1 , comprising contacting an unharvested tobacco material with a solution containing salt to give a treated tobacco material; harvesting and curing the treated tobacco material; subjecting the cured tobacco material to fermentation; and incorporating the fermented tobacco material into a smokeless tobacco product. 21. A method of modifying the bacterial content of a tobacco material, comprising: contacting an unharvested tobacco material less than about 24 hours before harvest with a salt solution comprising NaCl in a concentration of about 0.5% to about 15% by weight of the treatment solution, wherein said contacting provides a treated tobacco material having a reduced total bacterial content following harvest; harvesting the treated tobacco material; and curing the harvested, treated tobacco material to give a treated, cured tobacco material. 22. The method of claim 21 , wherein the unharvested tobacco material is selected from the group consisting of a tobacco seed, a tobacco seedling, an immature live plant, a mature live plant, or a portion thereof. 23. The method of claim 21 , wherein the total bacterial content of the treated tobacco material is reduced by at least about 50% in number following harvest. 24. The method of claim 21 , wherein the total bacterial content of the tobacco material comprises bacteria of the Lactobacillus genus, and wherein the Lactobacillus bacterial content of the treated tobacco material is increased following harvest. 25. The method of claim 21 , further comprising: processing the treated, cured tobacco material to provide a processed tobacco material in a form suitable for incorporation in a tobacco product; and incorporating the processed tobacco material into a smokeless tobacco product or a smoking article. 26. The method of claim 21 , further comprising: subjecting the treated, cured tobacco material to fermentation; and incorporating the fermented tobacco material into a smokeless tobacco product. 27. A method of modifying the bacterial content of a tobacco material, comprising contacting an unharvested tobacco material with a treatment solution comprising one or more probiotic Lactobacillus bacteria, wherein said contacting provides a treated tobacco material having a reduced total bacterial content following harvest. 28. The method of claim 27 , wherein the total bacterial content of the treated tobacco material is reduced by at least about 50% in number following harvest. 29. The method of claim 27 , wherein the treatment solution comprises Lactobacillus helveticus. 30. The method of claim 27 , wherein the treatment solution has a concentration of probiotic Lactobacillus bacteria of between about 1×10 5 colony forming units/mL and about 1×10 10 colony forming units/mL. 31. The method of claim 27 , further comprising curing the treated tobacco material to give a treated, cured tobacco material. 32. The method of claim 31 , wherein the tobacco-specific nitrosamine content of the treated, cured tobacco material is reduced relative to an untreated, cured tobacco material.

Assignees

Inventors

Classifications

  • A24B15/20Primary

    Biochemical treatment · CPC title

  • A24B15/183Primary

    sterilization, preservation or biological decontamination · CPC title

  • Preparation of tobacco on the plantation · CPC title

  • using microorganisms or enzymes as catalysts · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9155334B2 cover?
A method of modifying the content of certain bacteria in uncured tobacco material is provided, the method including contacting an uncured tobacco material with a treatment solution, wherein the treatment solution is selected from the group consisting of: (i) a solution comprising salt, sugar, or a combination thereof; (ii) a solution comprising one or more enzymes; and (iii) a solution comprisi…
Who is the assignee on this patent?
Moldoveanu Serban C, Riddick Marvin Glenn, Marshall Jerry Wayne, and 1 more
What technology area does this patent fall under?
Primary CPC classification A24B15/20. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Oct 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).