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95 results about "Colletotrichum sp." patented technology

Primer for detecting orchid colletotrichum gloeosporioides molecules and quick detection method

The invention relates to a primer for detecting orchid colletotrichum gloeosporioides molecules and a using method of the primer, which is specially used for detecting orchid colletotrichum gloeosporioides specific molecules and belongs to the fields of detection, identification and prevention and treatment of crop diseases. A pair of specific primers of orchid colletotrichum gloeosporioides comprising an upstream primer P1:5'-GGCCTCCCGCCTCCGGGCGGGTC-3' and a downstream primer P2:5'-TGAGGGCCTACATCAGCT-3' are subjected to polymerase chain reaction (PCR) amplification and agarose gel electrophoresis and can specifically amplify a specific amplification product with the segment length of 304bp in a plant infected with orchid colletotrichum gloeosporioides with pure DNA and germs and a culture medium. The specific molecule detection primer and the using method thereof can be used for detecting the orchid colletotrichum gloeosporioides in the plant infected with the orchid colletotrichum gloeosporioides and the culture medium quickly, sensitively and specifically, can also be used for performing early diagnosis on field diseases and monitoring and identifying germs, and provides reliable technological and theoretical basis for preventing and treating diseases caused by the orchid colletotrichum gloeosporioides.
Owner:INST OF PLANT PROTECTION FAAS

Primer and detection method for real-time fluorescent quantitative PCR detection of colletotrichum gloeosporioides of hevea brasiliensis

The invention discloses a primer and a detection method for real-time fluorescent quantitative PCR detection of colletotrichum gloeosporioides of a hevea brasiliensis. A specific primer is designed according to a ribosome ITS sequence of colletotrichum gloeosporioides of the hevea brasiliensis, quantitative analysis is performed on the colletotrichum gloeosporioides through real-time fluorescent quantitative PCR, and the change rule of DNA of the colletotrichum gloeosporioides in tissue after inoculation of leaves of the hevea brasiliensis along with time is determined. The hevea brasiliensiscolletotrichum gloeosporioides quantitative detection technology provided by the invention is high in specificity, high in sensitivity, high in repeatability, accurate in quantification, high in speedand capable of achieving a full-closed reaction, colletotrichum gloeosporioides is identified and can be accurately quantified, the thallus content of hevea brasiliensis leaves at different time points after thallus infection is obtained, and therefore, early warning and preventive measures are carried out when the disease does not appear, the loss caused by the disease is reduced to the minimum,and the method is of great significance to early diagnosis, disease prediction and comprehensive prevention and treatment of the disease.
Owner:HAINAN UNIVERSITY

Method for detecting bacillus subtilis Y13 volatile bacteriostatic substances based on HS-SPME and GC-MS

The invention belongs to the field of testing, and particularly discloses a method for detecting bacillus subtilis Y13 volatile bacteriostatic substances based on HS-SPME technology and GC-MS. According to the method, volatile substances of bacillus subtilis Y13 are collected by utilizing the HS-SPME technology, and GC-MS is used for detecting the components and amounts of the volatile substances.The method can comprehensively and accurately determine the components and amounts of the bacillus subtilis Y13 volatile substances, also can be completed in a normal-temperature range, and avoids the generation of a new compound in an analysis process. The working conditions of the HS-SPME technology provided by the invention can effectively enrich each component of the Y13 volatile substances;GC-MS detection adopts sectional heating, volatile substance components can be effectively separated, and the volatile substance components can be rapidly and accurately identified through corresponding mass spectrum parameters; in addition, colletotrichum fructicola is used as an indicator bacterium to identify the effective components of the bacillus subtilis Y13 volatile substances with strongbacteriostatic effect.
Owner:HAINAN KEDA FORESTRY CO LTD +1

Trichoderma fermentation medium for antagonizing tea colletotrichum bacteria and fermentation method

The invention discloses a trichoderma fermentation medium for antagonizing tea colletotrichum bacteria and a fermentation method, and relates to the technical field of microbial fermentation. According to key points of the technical scheme, the diameter of a tea colletotrichum bacterial colony treated by trichoderma fermentation liquor prepared by the fermentation medium and the fermentation method designed by the invention is 2.98-6.50 cm; the diameter of the tea colletotrichum bacterial colony is generally lower than the diameter 7.0 cm of a tea colletotrichum bacterial colony treated by trichoderma fermentation liquor prepared by an existing trichoderma culture medium, wherein the optimal fermentation medium is prepared from 200 g/L of potatoes, 18.34 g/L of glucose, 1.88 g/L of yeast extract, 0.86 g/L of dipotassium hydrogen phosphate and 0.63 g/L of ferrous sulfate. Under the condition, the diameter of the tea colletotrichum bacterial colony treated by the trichoderma fermentationliquor is 3.01 cm and is reduced by 13% compared with the diameter of the bacterial colony before optimization. A liquid fermentation medium is designed for trichoderma with an effect of antagonizingthe tea colletotrichum bacteria, so that the content of substances for inhibiting the growth of the tea colletotrichum bacteria in the trichoderma fermentation liquor is increased, the cost is savedto a certain extent, and the fermentation efficiency is improved.
Owner:贵州省生物技术研究所

PCR primer and quantitative detection method for rapidly detecting strawberry colletotrichum gloeosporioides

The invention relates to a PCR primer and quantitative detection method for rapidly detecting strawberry colletotrichum gloeosporioides. The PCR primer is designed according to a cutinase gene consensus sequence of colletotrichum gloeosporioides physiological races and comprises two primers Cfcut1 and Cfcut2 and an amplification product 115bp; by utilizing the PCR primer and the quantitative detection method, fungal genome DNA or field sample DNA can be subjected to PCR detection without separation and culture of pathogenic bacteria, the amplification efficiency is high, the specificity is good, the amplification efficiency of the primer is 99.47%, and colletotrichum gloeosporioides compound species causing strawberry anthracnose can be rapidly detected and identified; and through real-time fluorescent quantitative PCR, absolute quantitative detection can be carried out on the biomass of the colletotrichum gloeosporioides in a sample, the occurrence period and the prevalence intensityof the anthracnose are predicted timely and accurately, the anthracnose is prevented and treated and even avoided, negative influences caused by use of pesticide can be reduced, and a basis is provided for comprehensive prevention and treatment of the anthracnose.
Owner:SHANGHAI ACAD OF AGRI SCI
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