Banana is one of the most important crops in tropical and subtropical regions of China. Fenjiao( Musa Spp. ABB,Pisang Awak subgroup) has been grown by small scale famers because of its stable market price and better s...Banana is one of the most important crops in tropical and subtropical regions of China. Fenjiao( Musa Spp. ABB,Pisang Awak subgroup) has been grown by small scale famers because of its stable market price and better sugar-acid blend. However,the traditional Fenjiao variety is susceptible to banana Fusarium wilt,has a high plant height( over 5. 0 m),and farmers lack large-scale planting techniques.Based on the traditional Fenjiao variety,we selected‘Refen 1’variety through mutagenesis technology,which has low temperature resistance,suitable to marginal soils and relatively low plant height( 3. 2-4. 0 m). This paper mainly introduces the major techniques of propagation,cultivation,and post-harvest stages of‘Refen 1’banana,including the selection of explant materials,treatment,disinfection,initial culture,nursery hardening of in vitro-produced banana plants,and transplant of tissue culture seedlings. The major points of the cultivation technology include banana plantation selection and preparation,planting methods,irrigation and fertilizer management,pruning and retaining,and prevention and control of plant diseases and insect pests.展开更多
[Objective] The aim of experiment was to lay molecular foundation for studying maturity mechanism of banana after harvest. [Method] The combined method of suppressing subtractive hybridization and cDNA micro-array wer...[Objective] The aim of experiment was to lay molecular foundation for studying maturity mechanism of banana after harvest. [Method] The combined method of suppressing subtractive hybridization and cDNA micro-array were used to obtain cDNA segment of one PRMT gene in banana and the whole cDNA sequence of the gene was cloned.The bioinformatics analysis was operated on it,in addition, the expression profile analysis was conducted in different organs and different mature periods of banana.[Result] The whole length of cDNA in MaPRMT1 was 1 158 bp and possessed a complete open reading frame,which could encode 385 amino acids.It had high homology with PRMT in plant,containing one Methyltransf_1 domain.The MaPRMT1 gene was expressed in root,stem,leaf and fruit of banana and the expression levels in stem and leaf were relatively high.As the increase of days after harvest,the expression level declined gradually,however it reached maximum when ethylene release was biggest,then it declined.[Conclusion] MaPRMT1 belonged to the first kind of arginine methyltransferase and it was expressed differently in different organs and fruits at different mature periods.展开更多
[Objective] The paper was to identify strain HN-1 against banana wilt disease and to determine its antagonism. [Method] The strain HN-1 was ob- tained from the soil in fields heavily infected by Fusarium oxysporum f. ...[Objective] The paper was to identify strain HN-1 against banana wilt disease and to determine its antagonism. [Method] The strain HN-1 was ob- tained from the soil in fields heavily infected by Fusarium oxysporum f. sp. cubense （FOC）. Antagonism of the strain against F. oxysporum was tested via dual-cul- ture and inhibition test on spore germination. [Result] HN-1 effectively inhibited mycelial growth and spore germination of F. oxysporum, Strain HN-1 was identi- fied as BrevibaciUus brevis according to its characteristics in morphology, physiology and biochemistry and its 16S rDNA sequence. The strain showed high inhibition effect on 15 species of fungal pathogens in the dual-culture trials with fungal pathogens. [ Conclusion] The study provides theoretical basis for application of strain HN-1 in agricultural fields.展开更多
基金Supported by the Earmarked Fund for China Agriculture Research System(CARS-31-02)Key R&D project in Hainan Province(ZDYF2019060)Agricultural Science and Technology Innovation Program of CAAS "Evaluation and Regulation of Nutritional Quality of Major Agricultural Products"
文摘Banana is one of the most important crops in tropical and subtropical regions of China. Fenjiao( Musa Spp. ABB,Pisang Awak subgroup) has been grown by small scale famers because of its stable market price and better sugar-acid blend. However,the traditional Fenjiao variety is susceptible to banana Fusarium wilt,has a high plant height( over 5. 0 m),and farmers lack large-scale planting techniques.Based on the traditional Fenjiao variety,we selected‘Refen 1’variety through mutagenesis technology,which has low temperature resistance,suitable to marginal soils and relatively low plant height( 3. 2-4. 0 m). This paper mainly introduces the major techniques of propagation,cultivation,and post-harvest stages of‘Refen 1’banana,including the selection of explant materials,treatment,disinfection,initial culture,nursery hardening of in vitro-produced banana plants,and transplant of tissue culture seedlings. The major points of the cultivation technology include banana plantation selection and preparation,planting methods,irrigation and fertilizer management,pruning and retaining,and prevention and control of plant diseases and insect pests.
文摘[Objective] The aim of experiment was to lay molecular foundation for studying maturity mechanism of banana after harvest. [Method] The combined method of suppressing subtractive hybridization and cDNA micro-array were used to obtain cDNA segment of one PRMT gene in banana and the whole cDNA sequence of the gene was cloned.The bioinformatics analysis was operated on it,in addition, the expression profile analysis was conducted in different organs and different mature periods of banana.[Result] The whole length of cDNA in MaPRMT1 was 1 158 bp and possessed a complete open reading frame,which could encode 385 amino acids.It had high homology with PRMT in plant,containing one Methyltransf_1 domain.The MaPRMT1 gene was expressed in root,stem,leaf and fruit of banana and the expression levels in stem and leaf were relatively high.As the increase of days after harvest,the expression level declined gradually,however it reached maximum when ethylene release was biggest,then it declined.[Conclusion] MaPRMT1 belonged to the first kind of arginine methyltransferase and it was expressed differently in different organs and fruits at different mature periods.
基金Supported by Special Funds for Construction of Modern Agricultural Technology System(nycytx-24)Fundamental Research Special Project for Central Public-interest Scientific Institutes(ITBB130502)
文摘[Objective] The paper was to identify strain HN-1 against banana wilt disease and to determine its antagonism. [Method] The strain HN-1 was ob- tained from the soil in fields heavily infected by Fusarium oxysporum f. sp. cubense （FOC）. Antagonism of the strain against F. oxysporum was tested via dual-cul- ture and inhibition test on spore germination. [Result] HN-1 effectively inhibited mycelial growth and spore germination of F. oxysporum, Strain HN-1 was identi- fied as BrevibaciUus brevis according to its characteristics in morphology, physiology and biochemistry and its 16S rDNA sequence. The strain showed high inhibition effect on 15 species of fungal pathogens in the dual-culture trials with fungal pathogens. [ Conclusion] The study provides theoretical basis for application of strain HN-1 in agricultural fields.
