Method of increasing biomass and lipid content in a micro-organism and a genetically modified micro-organism exhibiting enhanced autophagy

US2016369307A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016369307-A1
Application numberUS-201515110683-A
CountryUS
Kind codeA1
Filing dateJan 9, 2015
Priority dateJan 10, 2014
Publication dateDec 22, 2016
Grant date

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.

According to an embodiment of the invention, there is provided a method of increasing biomass and lipid content in a micro-organism comprising cloning in a vector an exogenous gene sequence selected from the group comprising Atg1 gene, Atg6 gene, and Atg8 gene sequence wherein the sequence is codon optimized for said micro-organism, for inducing autophagy; introducing the vector containing the gene into the genome of the micro-organism to yield a genetically modified micro-organism; and growing the genetically modified micro-organism in suitable medium. According to another embodiment of the invention there is provided a method of increasing biomass and lipid content in a micro-organism exposed to stress, comprising treating the microorganism with an autophagy inducing agent.

First claim

Opening claim text (preview).

1 . A method of increasing biomass and lipid content in a micro-organism exposed to stress comprising: a. cloning in a vector an exogenous gene sequence selected from the group comprising Atg1 gene, Atg6 gene, and Atg8 gene sequence wherein the sequence is at least 50% homologous with Atg1 gene, Atg6 gene, and Atg8 gene, codon optimized for said micro-organism, for inducing autophagy; b. introducing the vector containing the gene into the genome of the micro-organism to yield a genetically modified micro-organism; and c. growing the genetically modified micro-organism in suitable medium. 2 . The method as claimed in claim 1 wherein, the genetically modified micro-organism is exposed to abiotic stresses comprisinq ultraviolet radiation (UV), salinity, light, unfavourable temperature, alkalinity, nutrient limitation, oxidative stress, senescence, sulfur deficiency, carbon deficiency, nitrogen use inefficiency, or stress due to biotic reasons comprising virus, bacteria, fungus or other stress causing pathogens. 3 . The method as claimed in claim 1 wherein, the vector is pChlamy_1. 4 . The method as claimed in claim 1 wherein, the exogenous gene has at least 52% homology with Atg1 gene of yeast. 5 . The method as claimed in claim 4 wherein, the exogenous gene having at least 52% homology with Atg1 gene of yeast is obtained from Chlorella. 6 . A method of increasing biomass and lipid content in a micro-organism exposed to stress, comprising treating the micro-organism with an autophagy inducing agent. 7 . The method as claimed in claim 6 wherein, the stress is abiotic stresses comprising ultraviolet radiation (UV), salinity, light, unfavourable temperature, alkalinity, nutrient limitation, oxidative stress, senescence, sulfur deficiency, carbon deficiency, nitrogen use inefficiency, or stress due to biotic reasons comprising virus, bacteria, fungus or other stress causing pathogens. 8 . The method as claimed in claim 6 wherein, the UV exposure is not more than 6 hours. 9 . The method as claimed in claim 6 wherein, the autophagy inducing agent is z-vad-fmk when the stress is UV. 10 . The method as claimed in claim 6 wherein, the micro-organism is treated with 1 mM to 1M of z-vad-fmk for 1 minute to 5 days. 11 . The method as claimed in claim 6 wherein, the micro-organism is kept in the dark for 24 hours after UV exposure followed by exposure to light. 12 . The method as claimed in claim 6 wherein, salinity exposure is not more than 10 days. 13 . The method as claimed in claim 6 wherein, the autophagy inducing agent is LiCl when the stress is salinity. 14 . A genetically modified micro-organism exhibiting enhanced autophagy, the micro-organism comprising a vector carrying an exogenous gene sequence selected from the group comprising Atg1 gene, Atg6 gene, and Atg8 gene sequence wherein the sequence is at least 50% homologous with Atg1 gene, Atg6 gene, and Atg8 gene codon optimized for algae, known to induce autophagy. 15 . The micro-organism as claimed in claim 14 wherein, the vector is pChlamy_1. 16 . The micro-organism as claimed in claim 14 wherein, the exogenous gene has at least 52% homology with Atg1 gene of yeast. 17 . The micro-organism as claimed in claim 14 wherein, the exogenous gene having at least 52% homology with Atg1 gene of yeast is obtained from Chlorella. 18 . A genetically modified eukaryotic micro-organism exhibiting enhanced autophagy comprising a nucleic acid sequence of SEQ ID No. 1. 19 . A genetically modified micro-organism exhibiting enhanced autophagy comprising a nucleic acid sequence coding a protein kinase domain of SEQ ID No. 2. 20 . The genetically modified micro-organism as claimed in claim 18 is a photosynthetic micro-organism. 21 . A nucleic acid sequence comprising SEQ ID No. 1. 22 . A nucleic acid sequence encoding a polypeptide comprising an amino acid sequence of SEQ ID No. 2 23 . A polypeptide comprising an amino acid sequence of SEQ ID No. 2 24 . A vector comprising a regulatory nucleic acid segment operably coupled to a nucleic acid sequence of SEQ ID No. 1. 25 . A vector comprising a regulatory nucleic acid segment operably coupled to a nucleic acid sequence encoding a polypeptide comprising an amino acid sequence of SEQ ID No. 2.

Assignees

Inventors

Classifications

  • from algae · CPC title

  • Unicellular algae; Culture media therefor (as new plants A01H13/00) · CPC title

  • involving modified lipid metabolism, e.g. seed oil composition · CPC title

  • C12P7/64Primary

    Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats · CPC title

  • Vectors or expression systems specially adapted for eukaryotic hosts · 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 US2016369307A1 cover?
According to an embodiment of the invention, there is provided a method of increasing biomass and lipid content in a micro-organism comprising cloning in a vector an exogenous gene sequence selected from the group comprising Atg1 gene, Atg6 gene, and Atg8 gene sequence wherein the sequence is codon optimized for said micro-organism, for inducing autophagy; introducing the vector containing the …
Who is the assignee on this patent?
Reliance Ind Ltd
What technology area does this patent fall under?
Primary CPC classification C12P7/64. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Dec 22 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).