The present invention relates to recombinant Gram-negative bacterial strains and its use in a method of treating cancer in a subject.

The present invention relates to recombinant Gram-negative bacterial strains and its use in a method of treating cancer in a subject.

Disclosed are double stranded RNA molecules that are toxic to hemipteran insects. In particular, interfering RNA molecules capable of interfering with pest target genes and that are toxic to the target pest are provided. Further, methods of making and using the interfering RNA, for example in transgenic plants or as the active ingredient in a composition, to confer protection from insect damage are disclosed.

Disclosed are methods and compositions related to polypeptides comprising a fusion of the needle tip protein and translocator protein of a type III secretion apparatus (T3SA) from a type III secretion system (T3SS) of a Gram negative bacteria. Disclosed herein are fusion polypeptides comprising a fusion of a needle tip protein, such as, Bsp22, LcrV, BipD, PcrV, CT053, or CT668, or anantigenic fragment thereof; and a translocator protein, such as, BopB, YopB, BipB, PopB, CopB, or CopB2, or anantigenic fragment thereof from a Type III secretion system (T3SS) of a Gram negative bacteria, such as, Bordetella, Burkholderia, Chlamydia, Pseudomonas, Vibrio, or Yersinia.

Compositions and methods for controlling pests are provided. The methods involve transforming organisms with a nucleic acid sequence encoding an insecticidal protein. In particular, the nucleic acid sequences are useful for preparing plants and microorganisms that possess insecticidal activity. Thus, transformed bacteria, plants, plant cells, plant tissues and seeds are provided. Compositions are insecticidal nucleic acids and proteins of bacterial species. The sequences find use in the construction of expression vectors for subsequent transformation into organisms of interest including plants, as probes for the isolation of other homologous (or partially homologous) genes. The pesticidal proteins find use in controlling, inhibiting growth or killing Lepidopteran, Coleopteran, Dipteran, fungal, Hemipteran and nematode pest populations and for producing compositions with insecticidal activity.

Compositions and methods for controlling pests are provided. The methods involve transforming organisms with a nucleic acid sequence encoding an insecticidal protein. In particular, the nucleic acid sequences are useful for preparing plants and microorganisms that possess insecticidal activity. Thus, transformed bacteria, plants, plant cells, plant tissues and seeds are provided. Compositions are insecticidal nucleic acids and proteins of bacterial species. The sequences find use in the construction of expression vectors for subsequent transformation into organisms of interest including plants, as probes for the isolation of other homologous (or partially homologous) genes. The pesticidal proteins find use in controlling, inhibiting growth or killing Lepidopteran, Coleopteran, Dipteran, fungal, Hemipteran and nematode pest populations and for producing compositions with insecticidal activity.

The present disclosure provides compositions and methods for introducing or enhancing Aca activity in prokaryotic cells. The provided compositions and methods can be used to inhibit Acr activity in prokaryotic cells, thereby enhancing endogenous or exogenous CRISPR-Cas activity. Cells, polynucleotides, plasmids, phage, and other elements for practicing the present methods are also provided.

The present disclosure provides proteins, protein fragments, protein variants, fusion proteins, nucleic acids, vectors, cells, methods, kits, and compositions for cleaving DNA and/or inhibiting growth of bacterial growth using IdrD protein or a fragment thereof. In some embodiments, the disclosure provides an IdrD protein comprising a fragment of IdrD protein from Proteus mirabilis, a fragment of an IdrD protein from Rothia, or a fusion thereof. In some embodiments, the disclosure provides a method for inhibiting bacterial biofilm formation on a surface, the method comprising contacting or coating the surface with an IdrD protein. In some embodiments, the disclosure provides a method for inhibiting bacterial biofilm formation on a surface, the method comprising contacting or coating the surface with an IdrD protein.

The present disclosure provides proteins, protein fragments, protein variants, fusion proteins, nucleic acids, vectors, cells, methods, kits, and compositions for cleaving DNA and/or inhibiting growth of bacterial growth using IdrD protein or a fragment thereof. In some embodiments, the disclosure provides an IdrD protein comprising a fragment of IdrD protein from Proteus mirabilis, a fragment of an IdrD protein from Rothia, or a fusion thereof. In some embodiments, the disclosure provides a method for inhibiting bacterial biofilm formation on a surface, the method comprising contacting or coating the surface with an IdrD protein. In some embodiments, the disclosure provides a method for inhibiting bacterial biofilm formation on a surface, the method comprising contacting or coating the surface with an IdrD protein.

The present disclosure discloses a Microcin MccY, and a preparation method and use thereof, wherein the amino acid sequence of the Microcin MccY is GGRGHIAEYFSGPITQVSFYG. Compared with Microcin MccJ25 that only has a bactericidal activity against a small part of serotypes of Salmonella such as Salmonella enteritidis, the Microcin MccY has bacteriostatic/bactericidal effects on Salmonella Pullorum, Salmonella typhimurium, Salmonella kentucky, Salmonella Infantis, Salmonella London, and Shigella sonnei, and can kill other serotypes of Salmonella that MccJ25 cannot kill. Especially, the Microcin MccY has an outstanding bactericidal effect on Salmonella typhimurium and Salmonella Pullorum which are common in livestock and poultry production, and meanwhile it also has bacteriostatic/bactericidal effects on Shigella sonnei. Therefore, the Microcin MccY overcomes the shortcoming of the narrow spectrum of the Microcin, has breakthrough significance, and has the potential as a substitute to antibiotics.