Use of uric acid for culturing bacteria sensitive to oxygen tension

US10626421B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10626421-B2
Application numberUS-201515304887-A
CountryUS
Kind codeB2
Filing dateApr 21, 2015
Priority dateApr 23, 2014
Publication dateApr 21, 2020
Grant dateApr 21, 2020

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.

The present invention relates to a method for cultivating in vitro in an acellular culture medium, bacteria for which the growth is sensitive to oxygen content, said bacterium being selected from anaerobic bacteria and intracellular micro-aerophilic bacteria, characterized in that uric acid is added into said acellular culture medium, and said bacterium is cultivated in said culture medium in the presence of oxygen.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for cultivating, in vitro, in an acellular culture medium, a strict anaerobic bacterium, wherein said strict anaerobic bacterium is cultivated in said acellular culture medium under an atmosphere comprising oxygen gas, and wherein uric acid at a concentration of at least 0.1 g/L is added to said acellular culture medium. 2. The method according to claim 1 , wherein the uric acid is added at a concentration of at least 0.2 g/L. 3. The method according to claim 1 , wherein the uric acid is added without any additional antioxidant compound in said acellular culture medium. 4. The method according to claim 1 , wherein the uric acid is added with at least one additional antioxidant compound in said culture medium. 5. The method according to claim 4 , wherein the uric acid is added in combination with at least one additional antioxidant compound selected from the group consisting of ascorbic acid and glutathion. 6. The method according to claim 4 , wherein the uric acid is added in combination with ascorbic acid and glutathion. 7. The method according to claim 1 , wherein said acellular medium is selected from the group consisting of: an axenic medium consisting of chemical or biological substances qualitatively and quantitatively defined, and a medium comprising an extract of milled or lysed material of pluricellular tissue. 8. The method according to claim 1 , wherein said strict anaerobic bacterium is an extracellular strict anaerobic bacterium, and wherein said culture medium comprises a member selected from the group consisting of an extract of milled or lysed material of pluricellular tissue, an enzymatic digested material of casein, soya, and/or animal tissue, a peptone, a yeast extract, a sugar, a salt NaCl, Na 2 PO 4 , and a combination thereof. 9. The method according to claim 1 , wherein said strict anaerobic bacterium is cultivated under an atmosphere of ambient air.

Assignees

Inventors

Classifications

  • C12N1/20Primary

    Bacteria; Culture media therefor · CPC title

  • Chemical stimulation of growth or activity by addition of chemical compounds which are not essential growth factors; Stimulation of growth by removal of a chemical compound (C12N1/34 takes precedence) · CPC title

  • C12P5/023Primary

    Methane · CPC title

  • Processes involving microorganisms of different genera in the same process, simultaneously · CPC title

  • Cross-Sectional Technologies · mapped topic

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 US10626421B2 cover?
The present invention relates to a method for cultivating in vitro in an acellular culture medium, bacteria for which the growth is sensitive to oxygen content, said bacterium being selected from anaerobic bacteria and intracellular micro-aerophilic bacteria, characterized in that uric acid is added into said acellular culture medium, and said bacterium is cultivated in said culture medium in t…
Who is the assignee on this patent?
Fond Mediterranee Infection, Univ Aix Marseille, Centre Nat Rech Scient, and 2 more
What technology area does this patent fall under?
Primary CPC classification C12N1/20. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 21 2020 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).