Genetic modification

遗传修饰
  • 文章类型: Journal Article
    虾青素是一种有价值的橙红色类胡萝卜素,在农业中具有广泛的应用。食物,化妆品,制药和营养食品领域。目前,虾青素的生物合成主要依靠雨生红球藻和枝状叶黄素菌。随着合成生物学的迅速发展,更多的重组微生物宿主已经被基因构建用于虾青素生产,包括大肠杆菌,酿酒酵母和解脂耶氏酵母。由于多个基因(15)参与虾青素的合成,采用不同的策略来平衡虾青素合成的代谢流尤为重要。此外,虾青素是一种储存在细胞内的脂溶性化合物,因此,有效的提取方法对于虾青素的经济生产也是必不可少的。近年来报道了几种高效绿色提取虾青素的方法,包括超流体提取,离子液体萃取和微波辅助萃取。因此,本文将全面介绍利用不同的微生物宿主和提高虾青素合成和提取效率的策略在虾青素生产和提取方面的研究进展。
    Astaxanthin is a valuable orange-red carotenoid with wide applications in agriculture, food, cosmetics, pharmaceuticals and nutraceuticals areas. At present, the biological synthesis of astaxanthin mainly relies on Haematococcus pluvialis and Xanthophyllomyces dendrorhous. With the rapid development of synthetic biology, more recombinant microbial hosts have been genetically constructed for astaxanthin production including Escherichia coli, Saccharomyces cerevisiae and Yarrowia lipolytica. As multiple genes (15) were involved in the astaxanthin synthesis, it is particularly important to adopt different strategies to balance the metabolic flow towards the astaxanthin synthesis. Furthermore, astaxanthin is a fat-soluble compound stored intracellularly, hence efficient extraction methods are also essential for the economical production of astaxanthin. Several efficient and green extraction methods of astaxanthin have been reported in recent years, including the superfluid extraction, ionic liquid extraction and microwave-assisted extraction. Accordingly, this review will comprehensively introduce the advances on the astaxanthin production and extraction by using different microbial hosts and strategies to improve the astaxanthin synthesis and extraction efficiency.
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  • 文章类型: Journal Article
    砷是一种广泛存在于地壳中的剧毒类金属,以及由于不同的人为活动而造成的污染(农用化学品的应用,采矿,废物管理)代表了一个新兴的环境问题。因此,需要不同的可持续和有效的修复方法和方法来防止和保护人类和其他生物免受有害砷的暴露。在众多的砷修复方法中,那些通过使用微生物作为吸附剂(微生物修复)支持的和/或植物作为绿色工厂(植物修复)被认为是具有成本效益和环境友好的生物修复。此外,遗传修饰和生物技术的最新进展已用于开发(i)更有效的转基因微生物和植物,可以(超)积累或解毒砷,和(ii)用于更有效地修复砷的新型有机矿物材料。在这次审查中,介绍了砷生物/植物修复的最新见解,以及砷生物途径中最相关的生理和分子机制,这可能是创造更多耐砷微生物和植物的有用起点,以及它们的共生关系进行了讨论。
    Arsenic is a highly toxic metalloid widespread in the Earth\'s crust, and its contamination due to different anthropogenic activities (application of agrochemicals, mining, waste management) represents an emerging environmental issue. Therefore, different sustainable and effective remediation methods and approaches are needed to prevent and protect humans and other organisms from detrimental arsenic exposure. Among numerous arsenic remediation methods, those supported by using microbes as sorbents (microbial remediation), and/or plants as green factories (phytoremediation) are considered as cost-effective and environmentally-friendly bioremediation. In addition, recent advances in genetic modifications and biotechnology have been used to develop (i) more efficient transgenic microbes and plants that can (hyper)accumulate or detoxify arsenic, and (ii) novel organo-mineral materials for more efficient arsenic remediation. In this review, the most recent insights from arsenic bio-/phytoremediation are presented, and the most relevant physiological and molecular mechanisms involved in arsenic biological routes, which can be useful starting points in the creation of more arsenic-tolerant microbes and plants, as well as their symbiotic associations are discussed.
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  • 文章类型: Journal Article
    用于检查特定信号传导途径在脉管系统中的作用和肺动脉高压(PH)发展的模型越来越多,这些模型基于具有不同遗传修饰的动物。本研究探讨了根据最常见的非遗传PH诱导剂,例如慢性暴露于缺氧或单次注射野百合碱,可通过遗传特定模型提供的PH相关病变的严重程度。对多种动物模型进行了516种干预措施的综述。它研究了旨在开发自发性PH的各种遗传驱动程序的优势,以及将此类程序与常见PH模型或其他刺激(“二次打击”)结合使用以加剧肺动脉重塑为目的的效果,右心室肥大和血流动力学或动物死亡率。广泛的转基因啮齿动物用于PH的临床前研究,与最常见的非遗传刺激相比,对遗传修饰的反应不同。然而,它们可以突出促进疾病病理生理特征表达的机制和途径,它们可能有助于识别新药的其他靶标。
    An increasing number of models used to examine the role of particular signaling pathways in vasculature and the development of pulmonary hypertension (PH) are based on animals with different genetic modifications. The present study explores the severity of PH-related lesions that can be provided by a genetic particular model in accordance to the most common non-genetic PH inducers such as chronic exposure to hypoxia or single injection of monocrotaline. A review of 516 interventions on a variety of animal models was performed. It examined the advantages of various genetically-driven procedures intended to develop spontaneous PH, and the effects of combining such procedures with common PH models or other stimuli (\'second-hit\') with the aim of exacerbating pulmonary artery remodeling, right ventricle hypertrophy and hemodynamics or animal mortality. A wide range of genetically-modified rodents are used for pre-clinical studies on PH, with different response to the genetic modification as compared to the most common non-genetic stimuli. Nevertheless, they could highlight the mechanisms and pathways that contribute to the expression of pathophysiological features of the disease, and they could be helpful in the identification of additional targets for new drugs.
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  • 文章类型: Journal Article
    鼻咽癌(NPC)是一种上皮性肿瘤,最常见的是从咽侧隐窝发展,并具有一些复杂的流行病学特征。其不寻常的种族和地理分布表明,不仅环境因素是这种罕见癌症类型发展的促成因素,而且遗传性状也起着重要的作用,以及含有亚硝胺的食物消费和EB病毒感染。患者可以呈现和遭受的体征和症状是各种各样的,包括鼻,otic,神经和一般;这种肿瘤的表现方式取决于肿瘤的阶段。适用于NPC的治疗管理需要根据患者的情况建立,包括放疗,化疗,手术,免疫疗法,靶向治疗或联合治疗。治疗的主要目的是局部和区域肿瘤控制;复发是远处转移未来发展的重要因素。一直在寻求新的治疗概念,目前专注于精准医学的研究,意味着根据肿瘤的特点,采用个性化的放射治疗方法进行全身治疗。
    Nasopharyngeal carcinoma (NPC) is an epithelial tumor, which develops most frequently from the lateral pharyngeal recess and holds some complex epidemiological characteristics. Its unusual race and geographic distribution suggests that not only the environmental factors are a contributing factor to the development of this rare cancer type, but also the genetic traits play an important role, along with nitrosamine-containing food consumption and Epstein-Barr virus infection. The signs and symptoms which a patient can present and suffer from are various and include nasal, otic, neurological as well as general ones; the way this tumor manifests being dependent on the stage of the tumor. The therapeutic management applicable in NPC needs to be established according to the case of the patient and include radiotherapy, chemotherapy, surgery, immune therapy, targeted therapy or combined treatment. The main objective of the treatment is local and regional tumor control; relapse is an important factor for future development of distant metastases. New therapeutic concepts are always sought of, current research focusing on precision medicine, meaning systemic treatment with a personalized radiotherapy approach according to the characteristics of the tumor.
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  • 文章类型: Journal Article
    UNASSIGNED: This article focused on the application scenarios of three-dimensional (3D) bioprinting and gene-editing technology in various medical fields, including gene therapy, tissue engineering, tumor microenvironment simulation, tumor model construction, cancer regulation and expression, osteogenesis, and skin and vascular regeneration, and summarizing its development prospects and shortcomings.
    UNASSIGNED: 3D bioprinting is a process based on additive manufacturing that uses biological materials as the microenvironment living cells. The scaffolds and carriers manufactured by 3D bioprinting technology provide a safe, efficient, and economical platform for genes, cells, and biomolecules. Gene modification refers to replacing, splicing, silencing, editing, controlling or inactivating genes and delivering new genes. The combination of this technology that changes cell function or cell fate or corrects endogenous mutations and 3D bioprinting technology has been widely used in various medical field.
    UNASSIGNED: We conducted a literature search for papers published up to March 2021 on the gene modification combined with 3D bioprinting in various medical fields via PubMed, Web of Science, China National Knowledge Infrastructure (CNKI). The following medical subject heading terms were included for a MEDLINE search: \"3D printing/gene editing\", \"3D printing/genetic modification\", \"3D printing/seed cell\", \"bioprinting/gene editing\", \"bioprinting/genetic modification\", \"bioprinting/seed cell\", \"scaffold/gene editing\", \"scaffold/genetic modification\", \"scaffold/seed cell\", \"gene/scaffold\", \"gene/bioprinting\", \"gene/3D printing\". Quantitative and qualitative data was extracted through interpretation of each article.
    UNASSIGNED: We have reviewed the application scenarios of 3D bioprinting and gene-editing technology in various medical fields, it provides an efficient and accurate delivery system for personalized tumor therapy, enhancing the targeting effect while maintaining the integrity of the fabricated structure. It exhibits significant application potential in developing tumor drugs. In addition, scaffolds obtained via 3D bioprinting provide gene therapy applications for skin and bone healing and repair and inducing stem cell differentiation. It also considers the future development direction in this field, such as the emergence and development of gene printing, 4D printing. The combination of nanotechnology and gene printing may provide a new way for future disease research and treatment.
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  • 文章类型: Journal Article
    Spider silk, as one of the hardest natural and biocompatible substances with extraordinary strength and flexibility, have become an ideal option in various areas of science and have made their path onto the biomedical industry. Despite its growing popularity, the difficulties in the extraction of silks from spiders and farming them have made it unaffordable and almost impossible for industrial scale. Biotechnology helped production of spider silks recombinantly in different hosts and obtaining diverse morphologies out of them based on different processing and assembly procedures. Herein, the characteristics of these morphologies and their advantages and disadvantages are summarized. A detailed view about applications of recombinant silks in skin regeneration and cartilage, tendon, bone, teeth, cardiovascular, and neural tissues engineering are brought out, where there is a need for strong scaffolds to support cell growth. Likewise, spider silk proteins have applications as conduit constructs, medical sutures, and 3D printer bioinks. Other characteristics of spider silks, such as low immunogenicity, hydrophobicity, homogeneity, and adjustability, have attracted much attention in drug and gene delivery. Finally, the challenges and obstacles ahead for industrializing the production of spider silk proteins in sufficient quantities in biomedicine, along with solutions to overcome these barriers, are discussed.
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  • 文章类型: Journal Article
    Mosquitoes are the vectors responsible for transmitting serious and life-threatening diseases such as malaria, dengue, yellow fever, chikungunya and lymphatic filariasis. Very few effective vaccines or drugs have been developed so far to prevent or treat these diseases, highlighting a need for vector control. This paper presents a comprehensive technology overview of patent documents disclosing biological agents for mosquito control. The patent analysis revealed that comparable number of patent documents were filed in two technology categories: non-recombinant agents and genetically modified (GM) agents. In the category of non-recombinant agents, toxic peptides from microbes and biological consortia seemed to be the earliest technology noted right from the year 1965 whereas the patent filings for suppression of mosquito population using genetic modification techniques have emerged from the year 2000 onwards. The United States of America is the leading patent filing jurisdiction followed by China and the Great Britain. Academic institutes have filed higher number of patent applications as compared to private companies. University of Florida was found to be the leading patent filing entity and its patents were focused on suppression of vector population using techniques such as release of insects with dominant lethal (RIDL) and RNA interference (RNAi).
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  • 文章类型: Journal Article
    A comprehensive review of available bioremediation technologies for the pesticide malathion is presented. This review article describes the usage and consequences of malathion in the environment, along with a critical discussion on modes of metabolism of malathion as a sole source of carbon, phosphorus, and sulfur for bacteria, and fungi along with the biochemical and molecular aspects involved in its biodegradation. Additionally, the recent approaches of genetic engineering are discussed for the manipulation of important enzymes and microorganisms for enhanced malathion degradation along with the challenges that lie ahead.
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  • 文章类型: Journal Article
    Genetic modification in plants was first recorded 10,000 years ago in Southwest Asia where humans first bred plants through artificial selection and selective breeding. Since then, advancements in agriculture science and technology have brought about the current GM crop revolution. GM crops are promising to mitigate current and future problems in commercial agriculture, with proven case studies in Indian cotton and Australian canola. However, controversial studies such as the Monarch Butterfly study (1999) and the Séralini affair (2012) along with current problems linked to insect resistance and potential health risks have jeopardised its standing with the public and policymakers, even leading to full and partial bans in certain countries. Nevertheless, the current growth rate of the GM seed market at 9.83-10% CAGR along with promising research avenues in biofortification, precise DNA integration and stress tolerance have forecast it to bring productivity and prosperity to commercial agriculture.
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  • 文章类型: Journal Article
    The hot topic of genetic modification and genome editing is sometimes presented as a rapid solution to various problems in the field of animal breeding and genetics. These technologies hold potential for future use in agriculture but we need to be aware of difficulties in large-scale application and integration in breeding schemes. In this review, we discuss applications of both classical genetic modifications (GM) using vectors and genome editing in dairy cattle breeding. We use an interdisciplinary approach considering both ethical and animal breeding perspectives. Decisions on how to make use of these techniques need to be made based not only on what is possible, but on what is reasonable to do. Principles of animal integrity, naturalness, risk perception, and animal welfare issues are examples of ethically relevant factors to consider. These factors also influence public perception and decisions about regulations by authorities. We need to acknowledge that we lack complete understanding of the genetic background of complex traits. It may be difficult, therefore, to predict the full effect of certain modifications in large-scale breeding programs. We present 2 potential applications: genome editing to dispense with dehorning, and insertion of human genes in bovine genomes to improve udder health as an example of classical GM. Both of these cases could be seen as beneficial for animal welfare but they differ in other aspects. In the former case, a genetic variant already present within the species is introduced, whereas in the latter case, transgenic animals are generated-this difference may influence how society regards the applications. We underline that the use of GM, as well as genome editing, of farm animals such as cattle is not independent of the context, and should be considered as part of an entire process, including, for example, the assisted reproduction technology that needs to be used. We propose that breeding organizations and breeding companies should take an active role in ethical discussions about the use of these techniques and thereby signal to society that these questions are being responsibly addressed.
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