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Energy crops for biofuel feedstocks: facts and recent patents on genetic manipulation to improve biofuel crops. 用于生物燃料原料的能源作物:改良生物燃料作物的基因操作的事实和最近的专利。
Pub Date : 2013-12-01 DOI: 10.2174/18722156113076660022
Suresh Kumar

Burning fossil-fuels to meet the global energy requirements by human being has intensified the concerns of increasing concentrations of greenhouse gases. Therefore, serious efforts are required to develop nonfossil-based renewable energy sources. Plants are more efficient in utilizing solar energy to convert it into biomass which can be used as feedstocks for biofuel production. Hence with the increasing demands of energy and the needs of cost-effective, sustainable production of fuels, it has become necessary to switch over to plant biomass as a renewable source of energy. Biofuels derived from more sustainable biological materials such as lignocellulosic plant residues, considered as second generation biofuels, are more dependable. However, there are technical challenges such as pretreatment and hydrolysis of lignocellulosic biomass to convert it into fermentable sugars. Plant genetic engineering has already proven its potential in modifying cell wall composition of plants for enhancing the efficiency of biofuel production. Interest and potential in the area are very much evident from the growing number of patents in the recent years on the subject. In this review, recent trends in genetic engineering of energy crops for biofuel production have been introduced, and strategies for the future developments have been discussed.

燃烧化石燃料以满足人类对全球能源的需求,加剧了人们对温室气体浓度增加的担忧。因此,需要大力发展非化石可再生能源。植物更有效地利用太阳能将其转化为可作为生物燃料生产原料的生物质。因此,随着能源需求的增加以及成本效益高、可持续生产燃料的需要,有必要改用植物生物量作为可再生能源。从更可持续的生物材料中提取的生物燃料,如木质纤维素植物残留物,被认为是第二代生物燃料,更可靠。然而,存在诸如预处理和水解木质纤维素生物质将其转化为可发酵糖的技术挑战。植物基因工程已经证明了其在改变植物细胞壁组成以提高生物燃料生产效率方面的潜力。近年来有关该主题的专利数量不断增加,这表明人们对该领域的兴趣和潜力非常明显。本文介绍了用于生物燃料生产的能源作物基因工程的最新发展趋势,并对未来的发展策略进行了讨论。
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引用次数: 0
Biotechnological advances in amaranths species and their future outlook in crop improvement--a review. 苋菜生物技术研究进展及其在作物改良中的应用前景
Pub Date : 2013-12-01 DOI: 10.2174/187221560703140204115514
R M Pandey

The grain amaranths were important food crops for the ancient middle and South American civilization. The germplasm of amaranths also has not been well characterized from the point of view of its exploitation for improvement of amaranths in general, a grain amaranth in particular. Among all under exploited crops grain amaranth is the most suitable candidate to begin with. As it is one of the most important under exploited crops being used as subsidiary or supplementary food. This work will report a study concerning the patent related to the biotechnological applications of Amaranths. It has been summarized in results that RAPD is a powerful approach to understand both inter-as-well as intra species relationships in the genus amaranths. One result indicates the presence of at least two repetitive families, such that at least one family of sequences is present in both cot1 as well as total nuclear DNA. The grain amaranth cultivation plays an important role in changing the economy of rural life. It is a source of dietary protein in strictly vegetarian people. In amaranths, somatic hybridization can be combined to the tertiary gene pools. Some of amaranth triploids are reported to be good in (Sharma SK, Dawson IK and Waugh R 1995) foliage and nutritional quality. They have broader leaves and good growth. Amaranth is grown under variety of soils and environmental conditions such as alkalinity, salinity, drought, frost etc. One of the ways to improve quality of grain amaranths to isolate variants of lysine genes products of which are enriched in essential amino acids. The high lysine content gene named as 'amargene' has been isolated and the patents have been used as biotechnological approach to introduce the gene in the tuber crop improvement The scope of biotechnology for the genetic improvement of grain amaranth crop has been described.

苋菜是古代中美洲和南美洲文明的重要粮食作物。从开发改良苋菜,特别是籽粒苋菜的角度来看,对苋菜的种质资源也没有很好的定性。在所有未开发的作物中,苋菜是最合适的候选作物。因为它是最重要的欠开发作物之一,被用作副食或补充食物。本文报道了紫红花生物技术应用相关专利的研究。研究结果表明,RAPD是了解苋菜属植物种间和种内关系的有效方法。一个结果表明至少存在两个重复家族,这样至少一个家族的序列存在于cot1和总核DNA中。粮食苋菜种植在改变农村经济生活中起着重要作用。它是严格素食者饮食中蛋白质的来源。在苋菜中,体细胞杂交可以结合到三级基因库中。据报道,一些苋菜三倍体的叶片和营养品质都很好(Sharma SK, Dawson IK和Waugh R 1995)。它们有更宽的叶子和良好的生长。苋菜生长在各种土壤和环境条件下,如碱性、盐度、干旱、霜冻等。从籽粒苋菜中分离富含必需氨基酸的赖氨酸基因变体是提高籽粒苋菜品质的途径之一。摘要分离出了高赖氨酸含量的“amargene”基因,并利用专利技术将该基因引入到块茎作物改良中,阐述了粮食苋菜作物遗传改良的生物技术范围。
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引用次数: 3
Patented aptamers for C-reactive protein detection: a review about their use in clinical diagnostics. c反应蛋白检测专利适体:临床诊断应用综述。
Pub Date : 2013-12-01 DOI: 10.2174/187221560703140204122543
Maria Viviana Miramontes-Espino, Marina Maria de Jesus Romero-Prado

C-reactive protein (CRP) is a homopentameric oligoprotein composed of monomeric subunits that are about 21 kD each. The form of detectable native CRP in validated assays was developed in 2007 and from that time has been considered as an excellent biomarker for peripheral artery disease and/or atherosclerosis, as well as a cardiovascular disease marker for risk prediction. The improvements in the detection of CRP levels could predict significantly the population that have increased risk of stroke being the modulation of CRP levels as a therapeutical outcome for prevention of cardiovascular diseases. Nowadays antibodies that specifically bind CRP, as monoclonal anti-CRP antibodies, are available from commercial sources. Aptamers are biomolecules conformed principally by RNA or DNA, able to adopt secondary structures that can bind to epitopes from oligopeptides or complete proteins. The sensitivity and accuracy of aptamers has let to consider them as more efficient to identify proteins than just antibodies. These properties have become the base for testing these molecules for different uses. A battery of patented aptamers has been developed for detecting and/or measuring CRP. In this sense, aptamers against CRP (CRP-apt) would help to modulate CRP physiological actions at systemic, tissue, cellular and molecular levels by using appropriate experimental designs. This kind of studies would lead to fully understand which systems are regulated by the protein, what disturbances are produced if the CRP is missing or overexpressed. Finally, we hallmark other applications of CRP in terms of patents for both basic and applied research.

c -反应蛋白(C-reactive protein, CRP)是一种均五聚体低聚蛋白,由每个约21 kD的单体亚基组成。可检测的天然CRP是在2007年开发出来的,从那时起就被认为是外周动脉疾病和/或动脉粥样硬化的优秀生物标志物,以及用于风险预测的心血管疾病标志物。CRP水平检测的改善可以显著预测卒中风险增加的人群,通过调节CRP水平作为预防心血管疾病的治疗结果。目前,可以从商业来源获得特异性结合CRP的抗体,如单克隆抗CRP抗体。适配体是主要由RNA或DNA构成的生物分子,能够采用二级结构,可以结合寡肽或完整蛋白质的表位。适配体的灵敏度和准确性使人们认为它们比抗体更有效地识别蛋白质。这些性质已经成为测试这些分子不同用途的基础。一组专利适体已经开发用于检测和/或测量CRP。从这个意义上说,通过适当的实验设计,抗CRP适体(CRP-apt)将有助于在系统、组织、细胞和分子水平上调节CRP的生理作用。这类研究将导致充分了解哪些系统是由蛋白质调节的,如果CRP缺失或过度表达会产生什么干扰。最后,我们在基础研究和应用研究方面对CRP的其他应用进行了专利标记。
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引用次数: 6
Recent advances in gene therapy of endometriosis. 子宫内膜异位症基因治疗进展。
Pub Date : 2013-12-01 DOI: 10.2174/18722156113079990021
Anastasia N Shubina, Anna A Egorova, Vladislav S Baranov, Anton V Kiselev

Endometriosis is a gynecological disease that affects up to 10%-15% of all reproductive-age women worldwide. It is characterized by the presence of endometrial tissues outside the uterine cavity. Endometriosis is a complex disease; its pathogenesis includes altered steroid metabolism and immune system abnormalities such as inflammation, increased angiogenic activity in the peritoneal fluid and impaired recognition of ectopic endometrial cells. The development of endometriosis also depends on genetic, anatomical and environmental factors. Numerous surgical and medical approaches to treat endometriosis have been developed to date. However, complete resolution of the problem has not been achieved so far. Gene therapy holds exciting promise for the treatment of numerous disorders and current studies have indicated it can also be applied to endometriosis. The focus of this review is to summarize the pathogenetic background of the disease and to highlight current gene therapy approaches for this common gynecological disorder.

子宫内膜异位症是一种妇科疾病,影响全世界10%-15%的育龄妇女。它的特点是子宫腔外存在子宫内膜组织。子宫内膜异位症是一种复杂的疾病;其发病机制包括类固醇代谢改变和免疫系统异常,如炎症、腹膜液血管生成活性增加和异位子宫内膜细胞识别受损。子宫内膜异位症的发生还与遗传、解剖和环境因素有关。迄今为止,已经开发了许多治疗子宫内膜异位症的手术和医学方法。然而,到目前为止,这个问题还没有完全解决。基因疗法在治疗许多疾病方面有着令人兴奋的前景,目前的研究表明它也可以应用于子宫内膜异位症。本文综述了该病的发病背景,并重点介绍了目前这种常见妇科疾病的基因治疗方法。
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引用次数: 24
Patent landscape for biological hydrogen production. 生物制氢专利景观。
Pub Date : 2013-12-01 DOI: 10.2174/187221560703140204124201
David B Levin, Simona Lubieniechi

Research and development of biological hydrogen production have expanded significantly in the past decade. Production of renewable hydrogen from agricultural, forestry, or other organic waste streams offers the possibility to contribute to hydrogen production capacity with no net, or at least with lower, greenhouse gas emissions. Significant improvements in the volumetric or molar yields of hydrogen production have been accomplished through genetic engineering of hydrogen synthesizing microorganisms. Although no commercial scale renewable biohydrogen production facilities are currently in operation, a few pilot scale systems have been demonstrated successfully, and while industrial scale production of biohydrogen still faces a number of technical and economic barriers, understanding the patent landscape is an important step in developing a viable commercialization strategy. In this paper, we review patents filed on biological hydrogen production. Patents on biohydrogen production from both the Canadian and American Patents databases were classified into three main groups: (1) patents for biological hydrogen by direct photolysis; (2) patents for biological hydrogen by dark fermentation; and (3) patents for process engineering for biological hydrogen production.

生物制氢的研究和开发在过去十年中有了显著的扩大。从农业、林业或其他有机废物流中生产可再生氢提供了一种可能性,即在没有净排放或至少减少温室气体排放的情况下,为氢生产能力做出贡献。通过合成氢微生物的基因工程,在体积或摩尔产氢量方面取得了显著的进步。虽然目前还没有商业规模的可再生生物氢生产设施在运行,但一些中试规模的系统已经成功地证明了这一点,尽管生物氢的工业规模生产仍然面临许多技术和经济障碍,但了解专利情况是制定可行的商业化战略的重要一步。本文对生物制氢方面的专利进行了综述。加拿大和美国专利数据库中的生物制氢专利可分为三大类:(1)直接光解生物制氢专利;(2)深色发酵生物制氢专利;(3)生物制氢工艺工程专利。
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引用次数: 2
Genetic algorithms with permutation coding for multiple sequence alignment. 多序列比对的排列编码遗传算法。
Pub Date : 2013-08-01 DOI: 10.2174/1872215611307020004
Mohamed Tahar Ben Othman, Gamil Abdel-Azim

Multiple sequence alignment (MSA) is one of the topics of bio informatics that has seriously been researched. It is known as NP-complete problem. It is also considered as one of the most important and daunting tasks in computational biology. Concerning this a wide number of heuristic algorithms have been proposed to find optimal alignment. Among these heuristic algorithms are genetic algorithms (GA). The GA has mainly two major weaknesses: it is time consuming and can cause local minima. One of the significant aspects in the GA process in MSA is to maximize the similarities between sequences by adding and shuffling the gaps of Solution Coding (SC). Several ways for SC have been introduced. One of them is the Permutation Coding (PC). We propose a hybrid algorithm based on genetic algorithms (GAs) with a PC and 2-opt algorithm. The PC helps to code the MSA solution which maximizes the gain of resources, reliability and diversity of GA. The use of the PC opens the area by applying all functions over permutations for MSA. Thus, we suggest an algorithm to calculate the scoring function for multiple alignments based on PC, which is used as fitness function. The time complexity of the GA is reduced by using this algorithm. Our GA is implemented with different selections strategies and different crossovers. The probability of crossover and mutation is set as one strategy. Relevant patents have been probed in the topic.

多序列比对(MSA)是生物信息学研究的热点之一。它被称为np完全问题。它也被认为是计算生物学中最重要和最艰巨的任务之一。关于这一点,已经提出了大量的启发式算法来寻找最优对齐。在这些启发式算法中有遗传算法(GA)。遗传算法主要有两个缺点:耗时长,可能导致局部最小值。MSA遗传过程的一个重要方面是通过增加和洗牌解编码(SC)的间隙来最大化序列之间的相似性。介绍了SC的几种方法。其中之一是排列编码(PC)。提出了一种基于遗传算法(GAs)与PC和2-opt算法的混合算法。PC机帮助编码MSA解决方案,从而最大限度地提高遗传算法的资源增益、可靠性和多样性。PC的使用打开了该区域通过应用所有功能的排列为MSA。因此,我们提出了一种基于PC计算多组队得分函数的算法,并将其作为适应度函数。该算法降低了遗传算法的时间复杂度。我们的遗传算法通过不同的选择策略和不同的交叉来实现。将交叉和变异的概率设为一种策略。本课题对相关专利进行了探讨。
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引用次数: 2
Pattern matching in indeterminate and Arc-annotated sequences. 不确定和arc注释序列中的模式匹配。
Pub Date : 2013-08-01 DOI: 10.2174/1872215611307020003
Md Tanvir Islam Aumi, Tanaeem M Moosa, M Sohel Rahman

In this paper, we present efficient algorithms for finding indeterminate Arc-Annotated patterns in indeterminate Arc-Annotated references. Our algorithms run in O(m+ (nm) w) time where n and m are respectively the length of our reference and pattern strings and w is the target machine word size. Here we have assumed the alphabet size to be constant, because, indeterminate Arc-Annotated sequences are used to model biological sequences. Clearly, for short patterns, our algorithms run in linear time and efficient algorithms for matching short patterns to reference genomes have huge applications in practical settings. We have also applied our algorithms to scan the ncRNAs without pseudoknots. We scanned three whole human chromosomes and it took only 2.5 - 4 minutes to scan one whole chromosome for an ncRNA family. Some relevant patents are discussed in.

在本文中,我们提出了在不确定的Arc-Annotated引用中寻找不确定的Arc-Annotated模式的有效算法。我们的算法在O(m+ (nm) w)时间内运行,其中n和m分别是我们的引用字符串和模式字符串的长度,w是目标机器字长。这里我们假设字母表的大小是恒定的,因为不确定的Arc-Annotated序列被用来模拟生物序列。显然,对于短模式,我们的算法在线性时间内运行,并且将短模式与参考基因组匹配的有效算法在实际环境中具有巨大的应用价值。我们也应用我们的算法来扫描没有假结的ncrna。我们扫描了三个完整的人类染色体,扫描一个ncRNA家族的整个染色体仅需2.5 - 4分钟。其中讨论了一些相关专利。
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引用次数: 0
Extraction of infrequent simple motifs from a finite set of sequences using a lattice structure. 用格结构从有限序列中提取不频繁的简单基元。
Pub Date : 2013-08-01 DOI: 10.2174/1872215611307020006
Tarek El-Falah, Thierry Lecroq, Mourad Elloumi

In this paper we present a method for finding infrequent simple motifs in a finite set of sequences. The method uses a lattice structure and minimal forbidden patterns. It is based on a method for solving the Simple Motif Problem and has the potential to discover new patents in biological macromolecules. Indeed, the extracted motifs can help biologists to learn about the biological functions of these macromolecules and, consequently, can help them to understand the mechanisms of the biological processes in which these sequences are involved.

本文给出了一种在有限序列集合中寻找不频繁简单基元的方法。该方法使用晶格结构和最小的禁止模式。它基于一种解决简单基序问题的方法,具有在生物大分子中发现新专利的潜力。事实上,提取的基序可以帮助生物学家了解这些大分子的生物学功能,从而可以帮助他们理解这些序列所涉及的生物过程的机制。
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引用次数: 1
GapMis: a tool for pairwise sequence alignment with a single gap. GapMis:一个工具,两两序列比对与一个单一的差距。
Pub Date : 2013-08-01 DOI: 10.2174/1872215611307020002
Tomás Flouri, Kimon Frousios, Costas S Iliopoulos, Kunsoo Park, Solon P Pissis, German Tischler

Motivation: Pairwise sequence alignment has received a new motivation due to the advent of recent patents in next-generation sequencing technologies, particularly so for the application of re-sequencing---the assembly of a genome directed by a reference sequence. After the fast alignment between a factor of the reference sequence and a high-quality fragment of a short read by a short-read alignment programme, an important problem is to find the alignment between a relatively short succeeding factor of the reference sequence and the remaining low-quality part of the read allowing a number of mismatches and the insertion of a single gap in the alignment.

Results: We present GapMis, a tool for pairwise sequence alignment with a single gap. It is based on a simple algorithm, which computes a different version of the traditional dynamic programming matrix. The presented experimental results demonstrate that GapMis is more suitable and efficient than most popular tools for this task.

动机:由于新一代测序技术专利的出现,成对序列比对获得了新的动机,特别是对于重测序的应用-由参考序列指导的基因组组装。在利用短读比对程序将参考序列的一个因子与短读片段的高质量片段快速比对之后,一个重要的问题是如何找到参考序列的一个相对较短的后续因子与剩余的低质量片段之间的比对,这些片段允许许多不匹配和在比对中插入单个间隙。结果:我们提出了GapMis,一种具有单个间隙的成对序列比对工具。它基于一种简单的算法,该算法计算传统动态规划矩阵的不同版本。实验结果表明,GapMis比大多数流行的工具更适合和有效地完成该任务。
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引用次数: 10
A computational approach to finding RNA tertiary motifs in genomic sequences: a case study. 在基因组序列中寻找RNA三级基序的计算方法:一个案例研究。
Pub Date : 2013-08-01 DOI: 10.2174/1872215611307020005
Kevin Byron, Christian Laing, Dongrong Wen, Jason T L Wang
Motif finding in DNA, RNA and proteins plays an important role in life science research. Recent patents concerning motif finding in biomolecular data are recorded in the DNA Patent Database which serves as a resource for policy makers and members of the general public interested in fields like genomics, genetics and biotechnology. In this paper, we present a computational approach to mining for RNA tertiary motifs in genomic sequences. Specifically, we describe a method, named CSminer, and show, as a case study, the application of CSminer to genome-wide search for coaxial helical stackings in RNA 3-way junctions. A coaxial helical stacking occurs in an RNA 3-way junction where two separate helical elements form a pseudocontiguous helix and provide thermodynamic stability to the RNA molecule as a whole. Experimental results demonstrate the effectiveness of our approach.
在DNA、RNA和蛋白质中寻找基序在生命科学研究中起着重要的作用。有关生物分子数据中基序发现的最新专利记录在DNA专利数据库中,该数据库为决策者和对基因组学、遗传学和生物技术等领域感兴趣的公众提供资源。在本文中,我们提出了一种计算方法来挖掘基因组序列中的RNA三级基序。具体来说,我们描述了一种名为CSminer的方法,并作为一个案例研究,展示了CSminer在全基因组搜索RNA 3-way连接中同轴螺旋堆叠的应用。同轴螺旋堆叠发生在RNA 3-way交界处,其中两个独立的螺旋元件形成假连续螺旋,并为RNA分子整体提供热力学稳定性。实验结果证明了该方法的有效性。
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引用次数: 2
期刊
Recent patents on DNA & gene sequences
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