IP Library Granted Patent US 10,385,310
Granted Patent B2
US 10,385,310 · App. 15/312,615 · Granted Aug 20, 2019

Decreased light-harvesting antenna size in cyanobacteria

Inventors: Anastasios Melis (El Cerrito, CA); Henning Kirst (Burgwedel, DE)
Assignee: The Regents of the University of California
C12N1/20C07K14/195C12N1/12C12N13/00C12N2510/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,385,310
App. No.
15/312,615
Granted
Aug 20, 2019
Kind
B2
Abstract

The invention provides methods and compositions for increasing photosynthetic efficiency and biomass production in cyanobacterial cultures by minimizing the phycobilisome light-harvesting antenna size through disruption of the phycocyanin-encoding CPC-operon.

Claims (15)

1. A method of enhancing biomass accumulation of a cyanobacteria culture, the method comprising:

providing a cyanobacteria cell population comprising cyanobacteria that are genetically modified in the genome to have a disruption in an endogenous CPC-operon comprising genes encoding CPCA, CPCB, CPCC1, CPCC2, and CPCD polypeptide components of phycocyanin-containing rods, wherein the disruption decreases phycobilisome antenna size compared to counterpart wild-type cyanobacteria comprising a native CPC-operon;

growing the cyanobacterial cell population in a reactor to obtain a cyanobacterial culture;

maintaining the cyanobacteria culture under conditions in which the photosynthetically active radiation (PAR) intensity is at least 500 micromol photons per square meter per second; and the culture absorbs at least 70% of the incoming light.

2. The method of claim 1 , wherein the PAR intensity is at least 800 micromol photons per square meter per second.

3. The method of claim 1 , wherein the culture absorbs at least 80%, or at least 90% of the incoming light.

4. The method of claim 1 , wherein the disruption in the endogenous CPC-operon is inhibition of a CPCA and/or CPCB gene.

5. The method of claim 1 , wherein the disruption in the endogenous CPC-operon is inhibition of at least one of a CPCC1, CPCC2, or CPCD gene.

6. The method of claim 1 , wherein the disruption in the endogenous CPC-operon is a deletion of at least one of a CPCA, CPCB, CPCC1, CPCC2, or CPCD genes.

7. The method of claim 1 , wherein the cyanobacteria are a species of a genus selected from the group consisting of Synechocystis, Synechococcus, Cyanothece , and Thermosynechococcus.

8. The method of claim 1 , wherein the cyanobacteria are a species of a genus of filamentous cyanobacteria.

9. The method of claim 8 , wherein the genus is selected from the group consisting of Arthrospira, Nostoc , and Anabaena.

10. The method of claim 1 , wherein the disruption is deletion of the endogenous CPC-operon.

11. The method of claim 1 , wherein the disruption in the endogenous CPC-operon comprises deletion of a CPCA or CPCB gene.

12. The method of claim 1 , wherein the endogenous CPC-operon encodes a CPCA polypeptide that has at least 70% identity to the amino acid sequence of SEQ ID NO:2 or encodes a CPCB polypeptide that has at least 70% identity to SEQ ID NO:3.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 6, 2020
From: UNIVERSITY OF CALIFORNIA BERKELEY
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 052324/0992 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2017
From: MELIS, ANASTASIOS; KIRST, HENNING
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 041701/0984 →
Continuity (2)
Provisional Application 62001326 · May 21, 2014
Related Publication 20170088812A1 · Mar 30, 2017
Cited By (1)
US 12,612,638