摘要:
The present disclosure generally relates to a planter (100) and method for growing plants (200) with air pruning. The planter (100) comprises an outer container (110) for a planting material (210) to grow the plants (200), and an inner container (120) to reduce the volume of the outer container (110). The inner container (120) comprises an inner space (130) and holes (132 / 134) to expose the plant roots (202) to air in the inner space (130) to air prune the exposed roots (202).
摘要:
Methods and compositions are provided for inhibiting or treating enterovirus infections, particularly EV71 and coxsackievirus infections, and diseases associated with enterovirus infections, including hand, foot and mouth disease (HFMD), polio, aseptic meningitis, encephalitis, acute flaccid paralysis, and acute cardiopulmonary dysfunction, using food dyes, particularly azo dyes and sulfonated azo dyes. Preferably, the food dyes are E102 Tartrazine, El 10 Sunset Yellow FCF, E122 Carmoisine, E123 Amaranth, El 24 Ponceau 4R, El 26 Ponceau 6R, El 29 Allura Red or E151 Brilliant Black BN (Black PN).
摘要:
The present invention relates to the field of fungal production fatty alcohols. More specifically, the present invention relates to genetically modified host cells, nucleic acid constructs and culture medium for the production of fatty alcohols in Rhodosporidium .
摘要:
The present invention relates to Enterovirus 71 (EV71), the development of an animal model and screening of candidate anti-EV71 compounds. More specifically, the present invention relates to the discovery that Enterovirus 71 (EV71 ) strains that have been adapted to infect rodent cell lines or cloned derived virus containing mutations in VP1 can cause disease in immuno-competent rodents.
摘要:
There is provided at least one isolated antibody or fragment thereof, wherein the antibody or fragment thereof is capable of specifically binding to at least one EV71 derived peptide. In particular the antibody or fragment thereof is capable of binding a conformational epitope on the VP3 capsid.
摘要:
The present invention provides nucleic acids and methods for conferring resistance to bacterial disease in plants. The present invention also provides promoters and promoter sequences useful for controlling expression in transgenic plants.
摘要:
The present invention relates to a universal H5N1 vaccine. More specifically, the present invention relates to the identification of three H5N1 strains which cover the entire variants in the neutralizing epitopes of hemagglutinin among most H5N1 lineages. The present invention further relates a universal H5N1 vaccine that comprises the three H5N1 strains or that comprises hemagglutinin peptides of each of these three strains.
摘要:
The present invention relates to the field of controlling pests, such as insects, using a virus to express pest genes in hosts. More specifically, the present invention relates to a method for rapidly screening for pest genes which can lead to mortality of the pest when the pest has ingested host tissues expressing virus-linked pest gene sequences. The present invention also relates to a method for controlling pests by viral expression of target pest sequences to modify endogenous expression of pest genes in cells or tissues of the pest.
摘要:
The present invention relates to the isolation of Jatropha curcas curcin genes and tissue-specific promoters and to the production of curcin-deficient Jatropha plants. More specifically, the present invention relates to the isolation of Jatropha curcas Curcin 1, Curcin 2 and Curcin 2 A. The present invention further relates to of the Curcin 1, Curcin 2 A and Curcin 2 genes and more particularly to tissue specific promoters of the Curcin 1 and Curcin 2A genes. The present invention further relates to production of curcin-deficient transgenic jatropha plants by using RNAi technology to suppress curcin gene expression.
摘要:
The present invention relates to the field of functional analysis of Jatropha genes on a genomic scale. More specifically, the present invention relates to a method for high-throughtput functional analysis of Jatropha curcas genes on a genomic scale using virus-induced gene silencing. The method involves use of the tobacco rattle virus (TRV).