Disclosed are genetically engineered microbial cells for the production of oligosaccharides comprising a galactose-β1,4-glucose moiety at their reducing end, wherein said microbial cells are able to produce said oligosaccharides in the absence of exogenously added lactose, and a method of producing said oligosaccharides using said microbial cells.

Compositions and methods relating to regulatable chimeric antigen receptors (RCARs), where the intracellular signaling or proliferation of the RCAR can be controlled to optimize the use of an RCAR-expressing cell to provide an immune response, are provided. For example, a RCAR can comprise a dimerization switch that, upon the presence of a dimerization molecule, can couple an intracellular signaling domain to an extracellular recognition element, e.g., an antigen binding domain, an inhibitory counter ligand binding domain, or costimulatory ECD domain. An RCAR can be engineered to include an appropriate antigen binding domain that is specific to a desired antigen target and used in the treatment of a disease.

Provided herein, in some embodiments, are enzymatic methods for producing an oligonucleotide comprising phosphoramidate-linked nucleotides, and compositions comprising the oligonucleotide thus produced.

High-fidelity, high-throughput nucleic acid sequencing enables healthcare practitioners and patients to gain insight into genetic variants and potential health risks. However, previous methods of nucleic acid sequencing often introduces sequencing errors (for example, mutations that arise during the preparation of a nucleic acid library, during amplification, or sequencing). Provided herein are sequencing adapters comprising a nondegenerate or variable length molecular barcode and compositions comprising a plurality of sequencing adapters, which can be useful for sequencing nucleic acids. Further provided are methods of using the sequencing adapters, including methods of sequencing nucleic acids, methods of identifying an error in a nucleic acid sequence, and methods of determining the number of nucleic acid molecules in a library.

This invention relates to compositions and methods for modifying root architecture in a plant through modification of an endogenous Ser-Thr protein kinase gene, such as endogenous PHOSPHOROUS STARVATION TOLERANCE 1 (PSTOL1) nucleic acids. The invention further relates to plants produced using the methods and compositions of the invention.

This invention relates to compositions and methods for modifying root architecture in a plant through modification of an endogenous Ser-Thr protein kinase gene, such as endogenous PHOSPHOROUS STARVATION TOLERANCE 1 (PSTOL1) nucleic acids. The invention further relates to plants produced using the methods and compositions of the invention.

Disclosed herein is a device for synthesizing ribonucleic acids (RNAs). According to embodiments of the present disclosure, the device comprises an in vitro transcription (IVT) module, a digestion module, and a processor. Optionally, the present device further comprises an IVT reaction monitoring means, a digestion reaction monitoring means, and/or a purifying means. Also disclosed herein are the methods of synthesizing RNA by use of the present device.

The present invention relates to Actinomycetales strains for the improved formation of acarbose. Provided are Actinomycetales strains which are engineered to overexpress dTDP-D-glucose-4,6-dehydratase (AcbB) and/or uridyltransferase (GtaB). Also provided are Actinomycetales strains which are engineered to have a reduced or absent expression of the small carbohydrate binding protein (Cgt) and/or a reduced or absent expression of genes which are essential for carotenoid synthesis. Also provided are tools, methods and means to generate these strains.

Provided herein are modified Archaeal family B polymerases derived from the Archaeal microorganism Thermococcus sp. EP1 that exhibit improved incorporation of nucleotide analogues utilized in DNA sequences.

This disclosure relates to thermophilic family B DNA polymerases comprising a neutral amino acid residue at a certain position near the C-terminus of the catalytic domain, which corresponds to a position occupied by a basic amino acid residue in wild-type Pfu polymerase. Related uses, methods, and compositions are also provided. In some embodiments, the polymerases comprise a 3′-5′ exonuclease domain and/or a sequence non-specific dsDNA binding domain.