A method of cultivating algal cells of an algae belonging to a class selected from Chlorophyceae, Euglenophyceae, Bacillariophyceae and Haptophyceae includes: irradiating the algal cells with an artificial light having a ratio of (i) photon flux density in a wavelength range of 520-630 nm to (ii) photosynthetic photon flux density, that is 65% or more; and measuring a cell size of the algal cells. Irradiation and non-irradiation of the algal cells with the artificial light are switched, or the photon flux density in the wavelength range of 520-630 nm is changed, according to the measured cell size.

The present invention provides a cell treatment apparatus capable of treating cells in a cell culture vessel. The cell treatment apparatus 100 according to the present invention includes a first region 1, a second region 3, and a third region 5. The first region 1 and the second region 3 are placed in succession. The first region 1 is a cell treatment chamber for treating cells. The cell treatment chamber can be closed from the outside of the cell treatment chamber and includes a culture vessel placement portion for placing a cell culture vessel. The second region 3 includes: a laser irradiation device capable of irradiating the cell culture vessel placed in the culture vessel placement portion with a laser; and a spot diameter adjustment device that adjusts a spot diameter formed in a portion to be irradiated with the laser in an object to be irradiated. The third region 5 includes a control device that controls at least one device in the cell treatment apparatus 100 and a power supply device 52 that supplies electric power to at least one device in the cell treatment apparatus 100. The culture vessel placement portion is placed to be adjacent to the second region 3 in the cell treatment chamber. An adjacent portion to the second region 3 in the culture vessel placement portion is translucent.

A method of cultivating algal cells of an algae belonging to a class selected from Chlorophyceae, Euglenophyceae, Bacillariophyceae and Haptophyceae includes: irradiating the algal cells with an artificial light having a ratio of (i) photon flux density in a wavelength range of 520-630 nm to (ii) photosynthetic photon flux density, that is 65% or more; and measuring a condition of the algal cells and/or a condition of an algal cell culture provided by cultivating the algal cells. Irradiation and non-irradiation of the algal cells with the artificial light are switched, or the photon flux density in the wavelength range of 520-630 nm is changed, according to the measured condition of the algal cells and/or the measured condition of the algal cell culture.

The present invention relates to the field of stem cells. More specifically, the present invention provides compositions and methods for using optogenetics to sustain the pluripotency of stem cells. In one embodiment, a vector comprises a nucleotide sequencing encoding a fusion protein comprising the intracellular domain of fibroblast growth factor 1 receptor (FGFR1) and a photoactivatable domain.

Systems and methods are provided for growing algae and/or other microorganisms in a controlled environment while reducing or minimizing the amount of energy required for maintaining desired conditions in the growth medium. The systems can be based on a photobioreactor having a “tube-in-tube structure”, where an outer cylindrical tube contains a heat regulation fluid that surrounds one or more inner cylinders that contain microorganisms in growth media. The heat regulation fluid in the outer cylinder, as well as the outer cylinder itself, can assist with regulating the temperature of the growth media in the inner cylinder(s).

Quantum dot (QD) LEDs useful for plant, algael and photosynthetic bacterial growth applications. The QD LEDs utilizes a solid state LED (typically emitting blue or UV light) as the primary light source and one or more QD elements as a secondary light source that down-converts the primary light. The emission profile of the QD LED can be tuned to correspond to the absorbance spectrum of one or more photosynthetic pigments of the organism.

Disclosed are methods and apparatuses for fabrication of polymer scaffolds and biological tissues in the multi-well plates in a rapid, high-throughput, controllable and reproducible manner by using optical exposure of the wells to patterned probe light without using a photomask. In some aspects, an apparatus includes a light source to produce a probe light; a digital display device to spatially modulate the probe light to encode a programmable spatial pattern in a spatially-modulated light; a stage to hold a target surface or chamber, wherein the target surface or chamber contains a solution including a material that forms a scaffold or construct based on interaction with the spatially-modulated light projected at the solution; and a computer control device in communication with the light source and the digital display device to control a change of the solution including the material to form the scaffold or construct.

Disclosed is a microalgae culture system using wavelength conversion which selectively provides light having a predetermined wavelength band depending on the species, the growth step and the health status of microalgae received in a reaction unit and a target material to be produced from the microalgae, so as to increase growth efficiency of the microalgae or to improve the output of the target material to be produced from the microalgae. The microalgae culture system includes a first culture sector including microalgae reaction units using a wavelength conversion material configured to transmit light of a first wavelength, a second culture sector including microalgae reaction units using a wavelength conversion material configured to transmit light of a second wavelength, and a control pump configured to transfer microalgae in the first culture sector to the second culture sector through a transmission pipe, when a control condition is achieved.

The present disclosure is generally directed to systems and methods for retrieving cells from a continuous culture microfluidic device. In some aspects, a system that allows for selective extraction of one or more cells of interest from an arbitrary population of cells using a high-throughput negative cell selection technique is disclosed herein. For example, the system may comprise a microfluidic device comprising a plurality of cell growth trenches configured to contain cells and a patterned light source capable of selectively killing unwanted cells contained within the device. Coupled with time-lapse imaging, one or more cells of interest within the device may, in some aspects, be identified and extracted with a relatively high extraction efficiency, e.g., at least 99.9% of cells of interest may be extracted from the plurality of cells. In addition, some aspects of the disclosure are directed to methods for using such a system.

The present invention relates to the field of stem cells. More specifically, the present invention provides compositions and methods for using optogenetics to sustain the pluripotency of stem cells. In one embodiment, a vector comprises a nucleotide sequencing encoding a fusion protein comprising the intracellular domain of fibroblast growth factor 1 receptor (FGFR1) and a photoactivatable domain.