红枣的营养成分及其保健功能

主要介绍红枣含有丰富的营养物质及生物活性成分,具有抗衰老作用、姗样作用、抗变态反应、抗肿瘤作用、免疫增强作用、增强肌肉力量、抗疲劳、保护肝脏、降压、镇静安神、抗惊厥等保健作用。     

药用植物内生真菌研究现状及其应用前景

随着对药用植物内生真菌研究的深入,从药用植物内生真菌中寻找新的生物活性成分已成为研究热点。内生真菌对药用植物的生长及活性成分的形成都有影响,内生真菌活性成分已成为发现新颖结构化合物及新药物的潜在资源。简要综述了近年来在内生真菌的分离鉴定、发酵、次生代谢产物、与宿主的关系等方面的研究进展。     

火棘植物功能性成分研究进展

火棘主要含黄酮、多糖、色素、多酚以及磷脂等功能性成分,具有酪氨酸酶抑制活性、抗氧化和抗疲劳活性、抗菌活性和预防肿瘤等作用。近年来,火棘的化学成分、活性研究及应用取得较大进展,本文通过对火棘的功能性成分、生物活性及应用进行了综述,以期为进一步研究和开发火棘资源提供参考。     

常见热加工方式对食源性活性成分影响的研究进展

食源性活性成分是来自于食物并具有调节人体机能，促进人体健康的一类具有生物活性的物质，主要包括生物活性肽、多糖、多酚、黄酮类物质等。热加工方式会引起食源性活性成分在食品中变化，如降解、氧化、美拉德反应等。因此，根据其热稳定性选择合适的加工方式对其应用至关重要。本文在对生物活性肽、多糖、多酚、黄酮类物质进行分类叙述的基础上，综述了杀菌、焙烤、蒸煮三种热加工条件下四种食源性活性成分含量、活性、结构变化的研究进展，以期对其在食品领域的合理利用和食品加工方式的改进提供理论参考。     

竹叶青属毒蛇的毒理机制与临床治疗新进展

作为中国南方常见毒蛇之一,竹叶青属毒蛇的毒液含有多种生物活性成分。近年来,随着研究的不断深入,竹叶青毒液中各生物活性成分的毒理机制正逐步被阐明。与此同时,竹叶青属毒蛇咬伤的临床治疗技术以及疗效亦在不断发展、提高。本文就近年来对竹叶青属毒蛇毒液活性成分的毒理学研究进展及相应的临床治疗手段等研究资料进行概括与综述。     

链霉菌来源生物碱及药理活性研究进展

不同来源的链霉菌所产生的次级代谢产物具有结构新颖、复杂多样且生物活性良好,是具有研究潜力的药物资源;生物碱类化合物是链霉菌代谢产物中重要活性成分之一。近十年从链霉菌中已经报道了许多生物碱的成分,本文按菌株来源综述了2007~2017年间报道的链霉菌来源的生物碱及其生物活性,为其他研究生物碱及其活性研究提供指导。     

米仔兰属化学成分及生物活性研究进展

米仔兰属植物在我国民间应用较多,已有不少学者从植物生态学和植物化学等方面对本属植物进行了广泛研究,但相关进展综述迄今尚未见报道。目前对米仔兰属植物化学成分及生物活性的报道较多集中于三萜类成分,该成分因其结构新奇成为米仔兰属所在楝科植物的特征性成分,因此其化学成分及生物活性均为当前研究热点。鉴于此,作者对国内外已报道的米仔兰属植物中化学成分及其生物活性研究进行归纳总结,特别关注其中三萜的不同类型及代表性活性,拟为进一步深入、系统地研究开发米仔兰属其它植物提供参考。     

香科科属植物化学成分及生物活性研究进展

近年来学术界对香科科属植物的化学成分和生理活性给予了很大关注。从该属植物中分离得封有萜类、黄酮类、苯丙素类化合物,生物活性测试表明该属植物具有抗氧化、抗菌消炎、解热镇痛、利胆利尿、降糖降压等活性,对昆虫具有拒食作用。本文综述了2000年来香科科属20余种植物成分及生物活性研究进展,为该属植物的研究与利用提供理论依据。     

一种白僵菌代谢产物中生物活性物质的研究 Ⅰ.具有清除自由基的活性物质的分离和制备

通过对白僵菌Beauveriasp.的液体培养及生物活性测定,发现该菌代谢产物具有较强的清除自由基的活性,我们用甲醇成功地提取出该活性成分,同时用色谱等方法对该活性成分进行了分离和制备,并用高压液相色谱法和DPPH薄层试验对其纯度及活性进行了检验,得到了具消除自由基活性的纯化合物P-24-3。     

响应面试验优化红枣乳酸发酵饮料工艺

为获得红枣乳酸发酵饮料的最佳工艺条件,以乳酸发酵饮料中的总酸含量为考察指标,在单因素试验的基础上,应用Box Behnken试验设计和响应面分析法对红枣乳酸发酵工艺进行优化,并对乳酸发酵前后的活性物质含量进行了比较。结果表明：各因素对红枣乳酸发酵饮料中总酸含量的影响大小依次为接种量、发酵温度、发酵时间,最佳工艺条件为发酵温度43℃、发酵时间24h、接种量10%,在此条件下,活性成分得到了很好地保留,制备得到的红枣乳酸发酵饮料中的总酸含量可达0.897g/100g,得到的回归模型对试验拟合较好。     

Prospects for application of breakthrough technologies in breeding: The CRISPR/Cas9 system for plant genome editing

Integration of the methods of contemporary genetics and biotechnology into the breeding process is assessed, and the potential role and efficacy of genome editing as a novel approach is discussed. Use of molecular (DNA) markers for breeding was proposed more than 30 years ago. Nowadays, they are widely used as an accessory tool in order to select plants by mono- and olygogenic traits. Presently, the genomic approaches are actively introduced into the breeding processes owing to automatization of DNA polymorphism analyses and development of comparatively cheap methods of DNA sequencing. These approaches provide effective selection by complex quantitative traits, and are based on the full-genome genotyping of the breeding material. Moreover, biotechnological tools, such as doubled haploids production, which provides fast obtainment of homozygotes, are widely used in plant breeding. Use of genomic and biotechnological approaches makes the development of varieties less time consuming. It also decreases the cultivated areas and financial expenditures required for accomplishment of the breeding process. However, the capacities of modern breeding are not limited to only these advantages. Experiments carried out on plants about 10 years ago provided the first data on genome editing. In the last two years, we have observed a sharp increase in the number of publications that report about successful experiments aimed at plant genome editing owing to the use of the relatively simple and convenient CRISPR/Cas9 system. The goal of some of these experiments was to modify agriculturally valuable genes of cultivated plants, such as potato, cabbage, tomato, maize, rice, wheat, barley, soybean and sorghum. These studies show that it is possible to obtain nontransgenic plants carrying stably inherited, specifically determined mutations using the CRISPR/Cas9 system. This possibility offers the challenge to obtain varieties with predetermined mono- and olygogenic traits.     

CRISPR/Cas基因编辑技术及其在作物育种中的应用

CRISPR/Cas基因编辑技术在植物基因功能研究和作物遗传改良方面具有重要应用价值,其主要依赖gRNA引导核酸内切酶在目标基因组位置产生双链断裂（DSBs）,DSBs在通过非同源末端连接（NHEJ）或同源重组（HDR）方式进行修复时,会引起靶标位置核苷酸序列的缺失、插入或者替换,从而实现基因编辑。介绍了CRISPR/Cas基因编辑技术的作用机理及发展趋势,并对CRISPR/Cas技术在主要粮食及经济作物育种中的应用进展进行了总结,以期为农作物育种提供有益的参考。     

Exploring the potential of CRISPR/Cas genome editing for vegetable crop improvement: An overview of challenges and approaches

Vegetables provide many nutrients in the form of fiber, vitamins, and minerals, which make them an important part of our diet. Numerous biotic and abiotic stresses can affect crop growth, quality, and yield. Traditional and modern breeding strategies to improve plant traits are slow and resource intensive. Therefore, it is necessary to find new approaches for crop improvement. Clustered regularly interspaced short palindromic repeats/CRISPR associated 9 (CRISPR/Cas9) is a genome editing tool that can be used to modify targeted genes for desirable traits with greater efficiency and accuracy. By using CRISPR/Cas9 editing to precisely mutate key genes, it is possible to rapidly generate new germplasm resources for the promotion of important agronomic traits. This is made possible by the availability of whole genome sequencing data and information on the function of genes responsible for important traits. In addition, CRISPR/Cas9 systems have revolutionized agriculture, making genome editing more versatile. Currently, genome editing of vegetable crops is limited to a few vegetable varieties (tomato, sweet potato, potato, carrot, squash, eggplant, etc.) due to lack of regeneration protocols and sufficient genome sequencing data. In this article, we summarize recent studies on the application of CRISPR/Cas9 in improving vegetable trait development and the potential for future improvement.     

Genome editing of polyploid crops: prospects,achievements and bottlenecks

Plant breeding aims to develop improved crop varieties. Many crops have a polyploid and often highly heterozygous genome, which may make breeding of polyploid crops a real challenge. The efficiency of traditional breeding based on crossing and selection has been improved by using marker-assisted selection (MAS), and MAS is also being applied in polyploid crops, which helps e.g. for introgression breeding. However, methods such as random mutation breeding are difficult to apply in polyploid crops because there are multiple homoeologous copies (alleles) of each gene. Genome editing technology has revolutionized mutagenesis as it enables precisely selecting targets. The genome editing tool CRISPR/Cas is especially valuable for targeted mutagenesis in polyploids, as all alleles and/or copies of a gene can be targeted at once. Even multiple genes, each with multiple alleles, may be targeted simultaneously. In addition to targeted mutagenesis, targeted replacement of undesirable alleles by desired ones may become a promising application of genome editing for the improvement of polyploid crops, in the near future. Several examples of the application of genome editing for targeted mutagenesis are described here for a range of polyploid crops, and achievements and bottlenecks are highlighted.

     

植物基因组编辑新工具——引导编辑技术

基于CRISPR/Cas9系统的引导编辑(prime editing,PE)技术作为一种新兴的基因组编辑技术,能在不产生双链断裂的情况下实现所有12种单碱基替换和小片段DNA的缺失或插入.引导编辑技术已经在多种植物中成功应用并将在植物精准育种中发挥重要作用.虽然植物引导编辑(plant prime editing,PP...     

动物基因组编辑中提升CRISPR/Cas9介导的同源重组效率研究进展*

基因组编辑技术可以对DNA或RNA进行精准改造,极大地促进了生命科学的发展。CRISPR/Cas9系统在靶位点诱导DNA发生双链或单链损伤,细胞对损伤部位采用无供体模板的非同源末端连接(non-homologous end joining,NHEJ)或有供体模板的同源重组(homologous recombination,HR)修复。基于HR的基因组编辑策略通常被用于获得DNA的精准改造,而NHEJ在动物DNA损伤修复中起主导作用。为了提升HR效率,研究人员设计了多种方案,包括CRISPR/Cas9系统优化和DNA修复通路调控等。从DNA损伤修复途径、Cas9变体选择、sgRNA设计、供体模板设计、DNA修复途径相关蛋白功能调控、供体模板募集效率提升、细胞周期调控及编辑细胞生存效率提升等方面详细综述了相关研究成果,发现尚未开发出放之四海而皆准的HR提升策略,基于HR的基因组编辑需要针对具体案例制定个体化策略。旨在为动物基因组编辑中提升CRISPR/Cas9介导的HR效率研究提供理论参考,为动物基因功能分析、基因治疗和经济动物基因编辑育种提供帮助。     

Current and future editing reagent delivery systems for plant genome editing

Many genome editing tools have been developed and new ones are anticipated; some have been extensively applied in plant genetics, biotechnology and breeding, especially the CRISPR/Cas9 system. These technologies have opened up a new era for crop improvement due to their precise editing of user-specified sequences related to agronomic traits. In this review, we will focus on an update of recent developments in the methodologies of editing reagent delivery, and consider the pros and cons of current delivery systems. Finally, we will reflect on possible future directions.