The present invention provides for a fully integrated microfluidic system capable of producing single-dose amounts of biotherapeutics at the point-of-care wherein protein production, purification and product harvest are all integrated as a single microfluidic device which is portable and capable of continuous-flow production of biotherapeutics at the microscale using a cell-free reaction system.

The present invention provides for a fully integrated microfluidic system capable of producing single-dose amounts of biotherapeutics at the point-of-care wherein protein production, purification and product harvest are all integrated as a single microfluidic device which is portable and capable of continuous-flow production of biotherapeutics at the microscale using a cell-free reaction system.

A multisensor and a process for the production of the multisensor for a bioreactor for use in cell culture and/or in microbiology is disclosed. The multisensor comprises at least three measurement arrangements configured to measure at least three parameters, where a first of the three measurement arrangements is configured to carry out an impedance measurement and/or a capacitive measurement, and where the first measurement arrangement has at least two electrodes which comprise an electrically conductive plasti.

The purpose of the present invention is to provide an automatic culture system whereby cells can be released from a vessel by a simple constitution and damage on the cells can be minimized In the automatic culture system according to the present invention, cells are cultured in a stimulus-responsive culture vessel and then the cells are released from the culture vessel by stimulating the culture vessel with a solution which is supplied from another vessel (see FIG. 3).

The present disclosure features methods and compositions for increasing the amount of products of cellular metabolism, e.g., proteins, by lowering the temperature of cells expressing the product at one or more steps while culturing the cells, expressing the product, and/or recovering the product.

Described herein are methods for using solid electrodes as an alternative source or sink of electrons to regulate the redox potential of mixed culture anaerobic reactors, so tunable fermentation products can be generated.

An extracellular potential measurement device includes multiple insulating films each of which is made from an electric insulating material, the insulating films being stacked and bonded to each other; and multiple electrode wires each of which is made from an electroconductive material, the electrode wires being arranged in multiple heights. Each of the electrode wires is interposed between an upper insulating film and a lower insulating film. Each of the insulating films, except for a lowermost insulating film, has an opening penetrating the insulating film. The opening in a lower insulating film has a size that is less than that of the opening in an upper insulating film, the openings in the insulating films being overlapped to form a recess having a size reducing downward, the recess being adapted to store a collection of cells. Each of the electrode wires has an end that is located near an opening in an insulating film that is immediately below the electrode wire, the ends being exposed in the recess.

Described herein are biofilm bioreactors for synthesis at the interface between two liquids, and methods of using such bioreactors for the biotransformation of feedstocks into chemical products. Also contemplated is the extraction of such products.

Improved methods for anaerobic digestion of organic matter to produce biogas. Among the improvements given are including ferric iron in a hydrolysis reactor to increase the rate and efficiency of anaerobic hydrolysis to provide substrates for methanogenesis. A solids separation step is added after hydrolysis and before methanogenesis to improve the efficiency of the methanogenesis step. Other improvements involve using separate tanks for the hydrolysis and methanogenesis stages and using two (or more) methanogenesis tanks in sequence, and switching the order of the two (or more) methanogenesis tanks periodically.

The United States faces significant environmental burden to treat and transport 0.61 billion kg of defective tomatoes (culled tomatoes) every year. The present disclosure provides for the treatment and processing of culled tomatoes in microbial-electrochemical systems, using the microbial fuel cell as a model reactor. The fundamental differences between the long-term oxidative behavior of unprocessed culled tomatoes compared to the three readily soluble substrates (dextrose, acetate, and wastewater) are disclosed. AC electrochemical impedance spectroscopy (EIS) analyses indicate the influential impedance contributions of the peel & seed to the cull oxidation. Cyclic voltammetry tests indicate that the indigenous redox-active pigments in the cull influence the faradaic processes involved in the cull oxidation.