Compositions and methods for controlling microbial growth

US2016208227A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016208227-A1
Application numberUS-201615000640-A
CountryUS
Kind codeA1
Filing dateJan 19, 2016
Priority dateJan 19, 2015
Publication dateJul 21, 2016
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

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Provided are modified microorganisms which are modified such that their growth can be controlled using exogenously provided compounds. The microorganisms can be modified by genetic alterations that include a promoter inducible by a first exogenously supplied compound. The promoter can be configured to drive expression of an RNA coding sequence that may be essential to growth of the microorganism. The microorganisms may also be modified to include site specific recombinase recognition sites flanking or within the RNA coding sequence so that expression of the corresponding site specific recombinase will disrupt transcription of the RNA. The site specific recombinase can be configured such that it expression and/or activity is suppressed by a second exogenously supplied compound. Methods of making the modified microorganisms and kits that contain reagents for making and using the modified microorganisms are also provided.

First claim

Opening claim text (preview).

What is claimed is: 1 . A modified microorganism, the growth of which can be controlled by exogenously provided first and second compounds, the modified microorganism having genetic alterations comprising: i) a promoter inducible by the first compound, wherein the inducible promoter is operably linked to an RNA coding sequence, expression of which is essential for growth of the microorganism, wherein the RNA coding sequence does not encode an auxotrophic marker; ii) a pair of site specific recombinase recognition sites (SSRRS) flanking or within the RNA coding sequence such that recombination between the SSRRS disrupts expression of the RNA coding sequence; and iii) a site specific recombinase (SSR) coding region, wherein the SSR is specific for the SSRS, and wherein expression of the SSR is repressed by the second compound. 2 . The modified microorganism of claim 1 , wherein a) the promoter is inducible by a sub-micromolar concentration of the first compound, or b) wherein the expression of the SSR is repressible by or inhibited by a sub-micromolar concentration of the second compound, or both a) and b). 3 . The modified microorganism of claim 1 , wherein the modified microorganism has the same or an enhanced growth rate relative to a microorganism of the same type that does not comprise the genetic alterations. 4 . The modified microorganism of claim 1 , wherein the modified microorganism is in an in vitro culture comprising a culture medium, wherein the culture medium comprises a sub-micromolar concentration of the first and/or second compounds. 5 . The modified microorganism of claim 4 , wherein the culture medium comprises a greater than sub-micromolar concentration of at least one decoy compound. 6 . The modified microorganism of claim 1 , further comprising at least one decoy RNA coding sequence or other decoy genetic element introduced into the microorganism, wherein if the decoy RNA coding sequence is present and expressed its expression is not affected by the first or the second compound. 7 . The modified microorganism of claim 1 , wherein the modified microorganism is a pathogenic microorganism. 8 . A kit for use in controlling growth of a microorganism of claim 1 , the kit comprising a plurality of compounds, wherein the plurality of compounds includes the first and second compounds, and further comprises at least one additional decoy compound, wherein the at least one additional decoy compound is included in a molar excess relative to the first and second compounds. 9 . The kit of claim 8 , further comprising at least 2, 3, 4 or 5 additional decoy compounds, wherein the additional compounds are each included in a molar excess relative to the first and second compounds. 10 . The kit of claim 8 , further comprising a microorganism of claim 1 . 11 . The kit of claim 8 , further comprising a growth medium. 12 . A method for controlling growth of a population of microorganisms of claim 1 , comprising culturing the population of microorganisms in a culture medium that comprises a sub-micromolar concentration of the first and second compounds. 13 . The method of claim 12 , wherein the first and second compounds are added to the culture medium in a composition that comprises at least one decoy compound, wherein the one decoy compound is included in a molar excess relative to the first and second compounds, and wherein the at least one decoy compound does not retard the growth of the microorganisms in the population. 14 . The method of claim 12 , wherein the population of microorganisms comprises pathogenic microorganisms.

Assignees

Inventors

Classifications

  • Genetically modified cells · CPC title

  • C12N9/1241Primary

    Nucleotidyltransferases (2.7.7) · CPC title

  • Nucleotidyltransferases (2.7.7) · CPC title

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What does patent US2016208227A1 cover?
Provided are modified microorganisms which are modified such that their growth can be controlled using exogenously provided compounds. The microorganisms can be modified by genetic alterations that include a promoter inducible by a first exogenously supplied compound. The promoter can be configured to drive expression of an RNA coding sequence that may be essential to growth of the microorganis…
Who is the assignee on this patent?
Univ New York, Univ Johns Hopkins
What technology area does this patent fall under?
Primary CPC classification C12N9/1241. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jul 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).