An imaging system and method for microbial growth detection, counting or identification. One colony may be contrasted in an image that is not optimal for another type of colony. The system and method provides contrast from all available material through space (spatial differences), time (differences appearing over time for a given capture condition) and color space transformation using image input information over time to assess whether microbial growth has occurred for a given sample.

An imaging system for imaging live biological systems comprises a detector array (12a) having an optical axis (X-X) and arranged to detect light and output detector signals, a support (10) arranged so support a biological system on the optical axis, an illuminating light source (16) located off the optical axis and arranged to direct at least partially-coherent light towards the biological system, and processing means (18) arranged to receive the detector signals and generate image data.

An imaging system and method for microbial growth detection, counting or identification. One colony may be contrasted in an image that is not optimal for another type of colony. The system and method provides contrast from all available material through space (spatial differences), time (differences appearing over time for a given capture condition) and color space transformation using image input information over time to assess whether microbial growth has occurred for a given sample.

An assembly and method to precisely and concurrently control the concentration, release, and depletion of chemical and biochemical species in localized regions in a three-dimensional volume of material using spatially patterned light. The system includes a container for holding a material comprising photo-responsive substance; the container is mounted to a motorized rotation stage that rotates the container along the z-axis at a predetermined rate; and a projector configured to project radiations at predefined wavelengths along an r-axis into the container while the container is rotating, wherein the radiations from multiple angles intersect to form localized photoreactive regions within a volume of the material.

One or more light sources may apply stimuli to a colony of organisms. The stimuli may include visible and non-visible light. The stimuli, taken together, may tend to favor survival of organisms that are adapted to perform photosynthesis which involves absorbing energy from infrared or ultraviolet light. In some cases, the set of stimuli may include illuminating the entire colony of organisms with green light, illuminating only a first portion of the colony with pulsed ultraviolet light, and illuminating only a second portion of the colony with pulsed infrared light.

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).

An improved cell culture monitoring system and method that detects cell growth and concentration in a dynamic environment of incubator/shaker. In order to reduce power consumption and make a wireless cell culture monitoring system practical, several methods of temperature compensation are used to replace a method of controlling the temperature of sensing module. Furthermore its power consumption can be significantly reduced by using an adaptive and synchronized light pulse detection technique.

Autotrophic algal growth in high incident light situations may be conducted in a reactor with circulation of algal reaction medium between light and dark zones with very short residence time in the light zone to maintain algal growth in the reactor in a linear growth regime in which the rate of algal biomass production is proportional to the incident photosynthetic photon flux density. Process monitoring and control may permit quick processing in a single step even in open pond systems. Dissolved nitrogen levels in product may be monitored and nitrogen nutrient input may be restricted to reduce dissolved nitrogen in effluent and to increase lipid yield without a separate nitrogen starvation step.

The invention relates to a bioreactor comprising a tank (100) capable of being operated for a working period, said tank (100) being intended to receive a culture medium comprising a cellular culture of photosynthetic microorganisms, a light source (200) arranged to emit incident light having a chosen incoming light intensity (Iin) in the direction of the tank, a temperature probe (400) for measuring the temperature of said culture medium in the tank, and a temperature regulator (500) capable of raising and lowering the temperature of said culture medium in the tank, and further comprising a control (700) of the temperature regulator arranged to adjust the temperature of the culture medium to a low setpoint value (VCB) during a first period, and to adjust the temperature of the culture medium to a high setpoint value (VCH) during a second period, the succession of said first and second periods making it possible to induce a cellular stress in at least some of said photosynthetic microorganisms during the working period.

Methods for laser-assisted repositioning of a micro-object and for culturing an attachment-dependent biological cell within a microfluidic device are described herein. Laser illumination is used to controllably create a bubble which repositions the micro-object. Further, methods of culturing an attachment-dependent biological cell are described, where the methods may include laser-assisted repositioning.