粤北地区食用菌产业及其循环经济发展概述     

余梓婷  潘林思  冯慧敏  李海渤 《蔬菜》2019,(10):31-35

从食用菌种类及其分布、产值、食用菌企业、食用菌产业循环经济发展情况等方面介绍了粤北地区食用菌产业发展现状,总结食用菌产业发展中存在的问题,如菌种问题突出,品牌意识缺乏;食用菌产业标准化落后;产品质量参差不齐,食品质量安全无保障;资源浪费严重;精深加工不足等,并提出相应的对策。  相似文献   

Transcriptome Analysis of Myzus persicae to UV-B Stress     

Chang-Li Yang  Jian-Yu Meng  Meng-Shuang Yao  Chang-Yu Zhang 《Journal of insect science (Online)》2021,21(3)

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Identification,characterization and full-length sequence analysis of a novel endornavirus in common sunflower (Helianthus annuus L.)     

Wen-wen LIU  Min XIN  Meng-ji CAO  Meng QIN  Hui LIU  Shou-qi ZHAO  Xi-feng WANG 《农业科学学报》2018,17(10):2281-2291

To identify the possible quarantine viruses in seven common sunflower varieties imported from the United States of America and the Netherlands, we tested total RNAs extracted from the leaf tissues using next-generation sequencing of small RNAs. After analysis of small RNA sequencing data, no any quarantine virus was found, but a double-stranded RNA(dsRNA) molecule showing typical genomic features of endornavirus was detected in two varieties, X3939 and SH1108. Full-length sequence and phylogenetic analysis showed that it is a novel endornavirus, temporarily named as Helianthus annuus alphaendornavirus(HaEV). Its full genome corresponds to a 14 662-bp dsRNA segment, including a 21-nt 5′ untranslated region(UTR), 3' UTR ending with the unique sequence CCCCCCCC and lacking a poly(A) tail. An open reading frame(ORF) that encodes a deduced 4 867 amino acids(aa) polyprotein with three domains: RdRP, Hel and UGT(UDP-glycosyltransferase). HaEV mainly distributed in the cytoplasm but less in the nucleus of leaf cells by fluorescence in situ hybridization(FISH) experiment. This virus has a high seed infection rate in the five varieties, X3907, X3939, A231, SH1108 and SR1320. To our knowledge, this is the first report about the virus of the family Endornaviridae in the common sunflower.  相似文献   

T7 RNA多聚酶基因的克隆、序列测定及其在E.coli中的表达     

余兴龙  涂长春  徐兴然  张茂林  张青婵  李作生 《中国兽医学报》2003,23(5):452-454

从BL21(DE3)E．coli菌株中以PCR的方法扩增得到了与T7RNA多聚酶(T7RNApolymerase，T7pol)基因大小一致的DNA片断。将PCR产物纯化后直接克隆到pGEM—T载体中，经酶切鉴定和DNA序列分析表明克隆得到了正确的T7pol基因。将T7pol基因亚克隆入pET-28b( )中，构建得到原核表达质粒pET28T7。该质粒的BL21(DE3)pLysS转化菌在IPTG的诱导下可表达约98800的蛋白，这与T7pol的相对分子质量一致。将该质粒转化DH5α、JMl09、HBl01、BL21(DE3)和BL21(DE3)pLysS等5种不同的宿主菌，仅有转化T7pol酶活性受到抑制的宿主菌BL21(DE3)pLysS才能得到转化子，而其余4种T7T7pol酶活性不受抑制的E．coli宿主菌不能得到转化子。pET28T7原核表达质粒这种仅能在T7pol酶活性受到抑制的宿主菌中才能存活的现象说明本试验所克隆的T7pol基因能正确表达出具有RNA转录酶活性的蛋白。  相似文献   

The RNA interference     

KONG Xiang-ping  Lixing W. Reneker 《园艺学报》2004,20(5):900-903

The phenomenon of RNA interference (RNAi) is highly conserved mechanism in the organism evolution. As a immune system, RNAi is a ubiquitous mechanism against invading microorganism in plant and animal cells. Recently, it has been found that RNAi is the process by which double-strand RNA(dsRNA) directs sequence-specific degradation of messenger RNA and the mediations of sequence specific messenger RNA degradation are 21-and 23-nucleotide small interfering RNAs that generate by ribonuclease from endogenous longer dsRNA or by transfectious technics from heterologous dsRNA. Over the past few years, the way in which cells respond to dsRNA by silencing homologous genes has revealed a new regulating paradigm in biology.  相似文献   

Effects on several cell lines by plasmid expressing bcl-xL short hairpin RNA     

LIU Fang  HE Cheng-wei  ZHANG Yue-fei  ZHOU Ke-yuan△ 《园艺学报》2006,22(6):1229-1231

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改良热硼酸法高效提取苹果果实RNA   总被引：17，自引：1，他引：17  

姚玉新  赵玲玲  郝玉金  翟衡 《果树学报》2005,22(6):737-740

苹果果实、尤其是成熟期的果实中多糖和其他次生物质含量高,难以提取RNA。对此,在原热硼酸法的基础上进行了改进,通过添加提取辅助剂并根据辅助剂特性调整提取步骤,高效、稳定地从苹果果实、尤其是后期果实中提取到了高质量的RNA。所得RNA的A260/A230大于2.0,A260/A280为1.8-2.1,并且RNA产量高,其中前期果实RNA产率在13.40μg/g以上,后期果实RNA产率在7.02μg/g以上,完全可以满足RT-PCR、cDNA-AFLP等分子生物学实验的要求。  相似文献   

Tobacco Plants Transformed with an Untranslatable Form of the Coat Protein Gene of the Potato Virus Y are Resistant to Viral Infection     

Khaled Masmoudi  Ines Yacoubi  Afif Hassairi  Lobna Naeit Elarbi  Radhouane Ellouz 《European journal of plant pathology / European Foundation for Plant Pathology》2002,108(4):285-292

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Expression of IL-6 mRNA in endometrium with endometriosis     

ZHENG Hui  LI Hong-yi  WANG Zi-neng  ZHAO Ying-she  YU Li  HE Si-cun  BAI Zhi-quan  ZHOU Zuo-yan  YAO Ping  WANG Yue-chun 《园艺学报》2002,18(5):553-555

AIM: The purpose of the present study was to explore the relationship between interleukin-6 mRNA expression and endometriosis. METHODS: Using the rat model, IL-6 mRNA expression in the endometrium was examined by RT-PCR. RESULTS: The expression of IL-6 mRNA in control rats did not change at 2, 4, 6 and 8 weeks after sham operation (P>0.05), but in model rats it gradually increased at 2, 4, 6 and 8 weeks after endometriosis (P<0.01). The expression of IL-6 mRNA in uterine endometrium with endometriosis was lower than in endometriotic tissue, but higher than in endometrium from healthy controls. CONCLUSION: The IL-6 mRNA expression may contribute to the development of endometriosis . The increase in IL-6 mRNA expression may promote the implantation and growth of endometriotic tissue.  相似文献   

两种一步法RNA提取试剂的比较   总被引：2，自引：0，他引：2  

孙映雪孙承英  赵永刚陈继明宋翠平  王志亮 《中国动物检疫》2004,21(12):22-23

RNA的提取在生物医学研究和临床检测上应用广泛。本文分别用进口Invitrogen公司生产的以及我们自己研制的一步法RNA提取试剂，提取大肠杆菌RNA、鸡肌肉组织RNA和尿囊液RNA，通过核酸电泳和荧光定量RT-PCR进行比较。结果表明用我们自己研制的和进口的试剂提取的RNA都不含有DNA；这些RNA都可以作为模板进行RT-PCR检测，并且在数量上相互之间没有明显差异。说明我们自己研制的一步法RNA提取试剂可以取代进口试剂。此外，本文还讨论了此类试剂一些评定方法。  相似文献