首页 > 最新文献

Microbiological reviews最新文献

英文 中文
Strategies for achieving high-level expression of genes in Escherichia coli. 实现大肠杆菌基因高水平表达的策略。
Pub Date : 1996-09-01 DOI: 10.1128/MMBR.60.3.512-538.1996
S. Makrides
Progress in our understanding of several biological processes promises to broaden the usefulness of Escherichia coli as a tool for gene expression. There is an expanding choice of tightly regulated prokaryotic promoters suitable for achieving high-level gene expression. New host strains facilitate the formation of disulfide bonds in the reducing environment of the cytoplasm and offer higher protein yields by minimizing proteolytic degradation. Insights into the process of protein translocation across the bacterial membranes may eventually make it possible to achieve robust secretion of specific proteins into the culture medium. Studies involving molecular chaperones have shown that in specific cases, chaperones can be very effective for improved protein folding, solubility, and membrane transport. Negative results derived from such studies are also instructive in formulating different strategies. The remarkable increase in the availability of fusion partners offers a wide range of tools for improved protein folding, solubility, protection from proteases, yield, and secretion into the culture medium, as well as for detection and purification of recombinant proteins. Codon usage is known to present a potential impediment to high-level gene expression in E. coli. Although we still do not understand all the rules governing this phenomenon, it is apparent that "rare" codons, depending on their frequency and context, can have an adverse effect on protein levels. Usually, this problem can be alleviated by modification of the relevant codons or by coexpression of the cognate tRNA genes. Finally, the elucidation of specific determinants of protein degradation, a plethora of protease-deficient host strains, and methods to stabilize proteins afford new strategies to minimize proteolytic susceptibility of recombinant proteins in E. coli.
我们对几个生物学过程的理解的进展有望扩大大肠杆菌作为基因表达工具的用途。有一个扩大的选择严格调控原核启动子适合实现高水平的基因表达。新的寄主菌株促进细胞质还原环境中二硫键的形成,并通过最小化蛋白质水解降解提供更高的蛋白质产量。深入了解蛋白质在细菌膜上的易位过程,可能最终使特定蛋白质在培养基中的强劲分泌成为可能。涉及分子伴侣的研究表明,在特定情况下,伴侣可以非常有效地改善蛋白质折叠,溶解度和膜运输。从这些研究中得出的负面结果也对制定不同的策略具有指导意义。融合伙伴可用性的显著增加提供了广泛的工具,用于改善蛋白质折叠,溶解度,保护蛋白酶,产量和分泌到培养基中,以及检测和纯化重组蛋白。密码子的使用被认为是大肠杆菌高水平基因表达的潜在障碍。虽然我们仍然不了解控制这一现象的所有规则,但很明显,“罕见”密码子,取决于它们的频率和环境,可以对蛋白质水平产生不利影响。通常,这个问题可以通过修饰相关密码子或同源tRNA基因的共表达来缓解。最后,蛋白质降解的特定决定因素的阐明,大量蛋白酶缺乏的宿主菌株,以及稳定蛋白质的方法,为减少重组蛋白在大肠杆菌中的蛋白水解敏感性提供了新的策略。
{"title":"Strategies for achieving high-level expression of genes in Escherichia coli.","authors":"S. Makrides","doi":"10.1128/MMBR.60.3.512-538.1996","DOIUrl":"https://doi.org/10.1128/MMBR.60.3.512-538.1996","url":null,"abstract":"Progress in our understanding of several biological processes promises to broaden the usefulness of Escherichia coli as a tool for gene expression. There is an expanding choice of tightly regulated prokaryotic promoters suitable for achieving high-level gene expression. New host strains facilitate the formation of disulfide bonds in the reducing environment of the cytoplasm and offer higher protein yields by minimizing proteolytic degradation. Insights into the process of protein translocation across the bacterial membranes may eventually make it possible to achieve robust secretion of specific proteins into the culture medium. Studies involving molecular chaperones have shown that in specific cases, chaperones can be very effective for improved protein folding, solubility, and membrane transport. Negative results derived from such studies are also instructive in formulating different strategies. The remarkable increase in the availability of fusion partners offers a wide range of tools for improved protein folding, solubility, protection from proteases, yield, and secretion into the culture medium, as well as for detection and purification of recombinant proteins. Codon usage is known to present a potential impediment to high-level gene expression in E. coli. Although we still do not understand all the rules governing this phenomenon, it is apparent that \"rare\" codons, depending on their frequency and context, can have an adverse effect on protein levels. Usually, this problem can be alleviated by modification of the relevant codons or by coexpression of the cognate tRNA genes. Finally, the elucidation of specific determinants of protein degradation, a plethora of protease-deficient host strains, and methods to stabilize proteins afford new strategies to minimize proteolytic susceptibility of recombinant proteins in E. coli.","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"6 1","pages":"512-38"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84798659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1182
Strategies for achieving high-level expression of genes in Escherichia coli. 实现大肠杆菌基因高水平表达的策略。
Pub Date : 1996-09-01 DOI: 10.1128/mr.60.3.512-538.1996
S C Makrides

Progress in our understanding of several biological processes promises to broaden the usefulness of Escherichia coli as a tool for gene expression. There is an expanding choice of tightly regulated prokaryotic promoters suitable for achieving high-level gene expression. New host strains facilitate the formation of disulfide bonds in the reducing environment of the cytoplasm and offer higher protein yields by minimizing proteolytic degradation. Insights into the process of protein translocation across the bacterial membranes may eventually make it possible to achieve robust secretion of specific proteins into the culture medium. Studies involving molecular chaperones have shown that in specific cases, chaperones can be very effective for improved protein folding, solubility, and membrane transport. Negative results derived from such studies are also instructive in formulating different strategies. The remarkable increase in the availability of fusion partners offers a wide range of tools for improved protein folding, solubility, protection from proteases, yield, and secretion into the culture medium, as well as for detection and purification of recombinant proteins. Codon usage is known to present a potential impediment to high-level gene expression in E. coli. Although we still do not understand all the rules governing this phenomenon, it is apparent that "rare" codons, depending on their frequency and context, can have an adverse effect on protein levels. Usually, this problem can be alleviated by modification of the relevant codons or by coexpression of the cognate tRNA genes. Finally, the elucidation of specific determinants of protein degradation, a plethora of protease-deficient host strains, and methods to stabilize proteins afford new strategies to minimize proteolytic susceptibility of recombinant proteins in E. coli.

我们对几个生物学过程的理解的进展有望扩大大肠杆菌作为基因表达工具的用途。有一个扩大的选择严格调控原核启动子适合实现高水平的基因表达。新的寄主菌株促进细胞质还原环境中二硫键的形成,并通过最小化蛋白质水解降解提供更高的蛋白质产量。深入了解蛋白质在细菌膜上的易位过程,可能最终使特定蛋白质在培养基中的强劲分泌成为可能。涉及分子伴侣的研究表明,在特定情况下,伴侣可以非常有效地改善蛋白质折叠,溶解度和膜运输。从这些研究中得出的负面结果也对制定不同的策略具有指导意义。融合伙伴可用性的显著增加提供了广泛的工具,用于改善蛋白质折叠,溶解度,保护蛋白酶,产量和分泌到培养基中,以及检测和纯化重组蛋白。密码子的使用被认为是大肠杆菌高水平基因表达的潜在障碍。虽然我们仍然不了解控制这一现象的所有规则,但很明显,“罕见”密码子,取决于它们的频率和环境,可以对蛋白质水平产生不利影响。通常,这个问题可以通过修饰相关密码子或同源tRNA基因的共表达来缓解。最后,蛋白质降解的特定决定因素的阐明,大量蛋白酶缺乏的宿主菌株,以及稳定蛋白质的方法,为减少重组蛋白在大肠杆菌中的蛋白水解敏感性提供了新的策略。
{"title":"Strategies for achieving high-level expression of genes in Escherichia coli.","authors":"S C Makrides","doi":"10.1128/mr.60.3.512-538.1996","DOIUrl":"https://doi.org/10.1128/mr.60.3.512-538.1996","url":null,"abstract":"<p><p>Progress in our understanding of several biological processes promises to broaden the usefulness of Escherichia coli as a tool for gene expression. There is an expanding choice of tightly regulated prokaryotic promoters suitable for achieving high-level gene expression. New host strains facilitate the formation of disulfide bonds in the reducing environment of the cytoplasm and offer higher protein yields by minimizing proteolytic degradation. Insights into the process of protein translocation across the bacterial membranes may eventually make it possible to achieve robust secretion of specific proteins into the culture medium. Studies involving molecular chaperones have shown that in specific cases, chaperones can be very effective for improved protein folding, solubility, and membrane transport. Negative results derived from such studies are also instructive in formulating different strategies. The remarkable increase in the availability of fusion partners offers a wide range of tools for improved protein folding, solubility, protection from proteases, yield, and secretion into the culture medium, as well as for detection and purification of recombinant proteins. Codon usage is known to present a potential impediment to high-level gene expression in E. coli. Although we still do not understand all the rules governing this phenomenon, it is apparent that \"rare\" codons, depending on their frequency and context, can have an adverse effect on protein levels. Usually, this problem can be alleviated by modification of the relevant codons or by coexpression of the cognate tRNA genes. Finally, the elucidation of specific determinants of protein degradation, a plethora of protease-deficient host strains, and methods to stabilize proteins afford new strategies to minimize proteolytic susceptibility of recombinant proteins in E. coli.</p>","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"60 3","pages":"512-38"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC239455/pdf/600512.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19807799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 66
Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia. 囊性纤维化的微生物发病机制:粘液样铜绿假单胞菌和洋葱伯克氏菌。
Pub Date : 1996-09-01 DOI: 10.1128/MMBR.60.3.539-574.1996
J. Govan, V. Deretic
Respiratory infections with Pseudomonas aeruginosa and Burkholderia cepacia play a major role in the pathogenesis of cystic fibrosis (CF). This review summarizes the latest advances in understanding host-pathogen interactions in CF with an emphasis on the role and control of conversion to mucoidy in P. aeruginosa, a phenomenon epitomizing the adaptation of this opportunistic pathogen to the chronic chourse of infection in CF, and on the innate resistance to antibiotics of B. cepacia, person-to-person spread, and sometimes rapidly fatal disease caused by this organism. While understanding the mechanism of conversion to mucoidy in P. aeruginosa has progressed to the point where this phenomenon has evolved into a model system for studying bacterial stress response in microbial pathogenesis, the more recent challenge with B. cepacia, which has emerged as a potent bona fide CF pathogen, is discussed in the context of clinical issues, taxonomy, transmission, and potential modes of pathogenicity.
铜绿假单胞菌和洋葱伯克霍尔德菌的呼吸道感染在囊性纤维化(CF)的发病机制中起主要作用。本文综述了CF中宿主-病原体相互作用的最新进展,重点介绍了铜绿假单胞菌(P. aeruginosa)向粘液样质的转化的作用和控制,这一现象体现了这种机会性病原体对CF慢性感染过程的适应,以及该菌对抗生素的先天耐药、人际传播和有时由该菌引起的快速致命疾病。虽然对P. aeruginosa向粘液样质的转化机制的理解已经取得了进展,这种现象已经演变为研究微生物发病机制中细菌应激反应的模型系统,但最近对洋葱芽孢杆菌的挑战已经成为一种有效的CF病原体,在临床问题,分类,传播和潜在的致病性模式的背景下进行了讨论。
{"title":"Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia.","authors":"J. Govan, V. Deretic","doi":"10.1128/MMBR.60.3.539-574.1996","DOIUrl":"https://doi.org/10.1128/MMBR.60.3.539-574.1996","url":null,"abstract":"Respiratory infections with Pseudomonas aeruginosa and Burkholderia cepacia play a major role in the pathogenesis of cystic fibrosis (CF). This review summarizes the latest advances in understanding host-pathogen interactions in CF with an emphasis on the role and control of conversion to mucoidy in P. aeruginosa, a phenomenon epitomizing the adaptation of this opportunistic pathogen to the chronic chourse of infection in CF, and on the innate resistance to antibiotics of B. cepacia, person-to-person spread, and sometimes rapidly fatal disease caused by this organism. While understanding the mechanism of conversion to mucoidy in P. aeruginosa has progressed to the point where this phenomenon has evolved into a model system for studying bacterial stress response in microbial pathogenesis, the more recent challenge with B. cepacia, which has emerged as a potent bona fide CF pathogen, is discussed in the context of clinical issues, taxonomy, transmission, and potential modes of pathogenicity.","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"1 1","pages":"539-74"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91092607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1771
Microbial metabolism of pyridine, quinoline, acridine, and their derivatives under aerobic and anaerobic conditions. 吡啶、喹啉、吖啶及其衍生物在好氧和厌氧条件下的微生物代谢。
Pub Date : 1996-09-01 DOI: 10.1128/mr.60.3.483-498.1996
J P Kaiser, Y Feng, J M Bollag

Our review of the metabolic pathways of pyridines and aza-arenes showed that biodegradation of heterocyclic aromatic compounds occurs under both aerobic and anaerobic conditions. Depending upon the environmental conditions, different types of bacteria, fungi, and enzymes are involved in the degradation process of these compounds. Our review indicated that different organisms are using different pathways to biotransform a substrate. Our review also showed that the transformation rate of the pyridine derivatives is dependent on the substituents. For example, pyridine carboxylic acids have the highest transformation rate followed by mono-hydroxypyridines, methylpyridines, aminopyridines, and halogenated pyridines. Through the isolation of metabolites, it was possible to demonstrate the mineralization pathway of various heterocyclic aromatic compounds. By using 14C-labeled substrates, it was possible to show that ring fission of a specific heterocyclic compound occurs at a specific position of the ring. Furthermore, many researchers have been able to isolate and characterize the microorganisms or even the enzymes involved in the transformation of these compounds or their derivatives. In studies involving 18O labeling as well as the use of cofactors and coenzymes, it was possible to prove that specific enzymes (e.g., mono- or dioxygenases) are involved in a particular degradation step. By using H2 18O, it could be shown that in certain transformation reactions, the oxygen was derived from water and that therefore these reactions might also occur under anaerobic conditions.

我们对吡啶和氮杂芳烃代谢途径的回顾表明,杂环芳烃的生物降解在好氧和厌氧条件下都发生。根据环境条件,不同类型的细菌、真菌和酶参与这些化合物的降解过程。我们的综述表明,不同的生物体使用不同的途径来生物转化底物。我们的回顾还表明,吡啶衍生物的转化速率依赖于取代基。例如,吡啶羧酸的转化率最高,其次是单羟基吡啶、甲基吡啶、氨基吡啶和卤代吡啶。通过代谢物的分离,可以证明各种杂环芳香族化合物的矿化途径。通过使用14c标记的底物,可以证明特定杂环化合物的环裂变发生在环的特定位置。此外,许多研究人员已经能够分离和表征参与这些化合物或其衍生物转化的微生物甚至酶。在涉及18O标记以及使用辅助因子和辅酶的研究中,有可能证明特定的酶(例如,单加氧酶或双加氧酶)参与特定的降解步骤。通过使用H2 18O,可以证明在某些转化反应中,氧来源于水,因此这些反应也可能在厌氧条件下发生。
{"title":"Microbial metabolism of pyridine, quinoline, acridine, and their derivatives under aerobic and anaerobic conditions.","authors":"J P Kaiser,&nbsp;Y Feng,&nbsp;J M Bollag","doi":"10.1128/mr.60.3.483-498.1996","DOIUrl":"https://doi.org/10.1128/mr.60.3.483-498.1996","url":null,"abstract":"<p><p>Our review of the metabolic pathways of pyridines and aza-arenes showed that biodegradation of heterocyclic aromatic compounds occurs under both aerobic and anaerobic conditions. Depending upon the environmental conditions, different types of bacteria, fungi, and enzymes are involved in the degradation process of these compounds. Our review indicated that different organisms are using different pathways to biotransform a substrate. Our review also showed that the transformation rate of the pyridine derivatives is dependent on the substituents. For example, pyridine carboxylic acids have the highest transformation rate followed by mono-hydroxypyridines, methylpyridines, aminopyridines, and halogenated pyridines. Through the isolation of metabolites, it was possible to demonstrate the mineralization pathway of various heterocyclic aromatic compounds. By using 14C-labeled substrates, it was possible to show that ring fission of a specific heterocyclic compound occurs at a specific position of the ring. Furthermore, many researchers have been able to isolate and characterize the microorganisms or even the enzymes involved in the transformation of these compounds or their derivatives. In studies involving 18O labeling as well as the use of cofactors and coenzymes, it was possible to prove that specific enzymes (e.g., mono- or dioxygenases) are involved in a particular degradation step. By using H2 18O, it could be shown that in certain transformation reactions, the oxygen was derived from water and that therefore these reactions might also occur under anaerobic conditions.</p>","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"60 3","pages":"483-98"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC239453/pdf/600483.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19809132","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 36
RNA-protein interactions in regulation of picornavirus RNA translation. RNA-蛋白相互作用调控小核糖核酸翻译。
Pub Date : 1996-09-01 DOI: 10.1128/MMBR.60.3.499-511.1996
G. Belsham, N. Sonenberg
The translation of picornavirus RNA occurs by a cap-independent mechanism directed by a region of about 450 nucleotides from the 5' untranslated region, termed an internal ribosome entry site (IRES). Internal initiation of protein synthesis occurs without any requirement for viral proteins. Furthermore, it is maintained when host cell protein synthesis is almost abolished. By using in vitro translation systems, two distinct families of IRES elements which have very different predicted RNA secondary structures have been defined. The cardiovirus and aphthovirus elements function very efficiently in rabbit reticulocyte lysate, whereas the enterovirus and rhinovirus elements function poorly in this system. However, supplementation of this translation system with additional cellular proteins can stimulate translation directed by the enterovirus and rhinovirus RNAs and reduce production of aberrant initiation products. The characterization of cellular proteins interacting with the picornavirus IRES is a major focus of research. Many different protein species can be observed to interact with regions of the IRES by in vitro analyses, e.g., UV cross-linking. However, the function and significance of many of these interactions are not always known. For two proteins, La and the polypyrimidine tract-binding protein, evidence has been obtained for a functional role of their interaction with IRES elements.
小核糖核酸RNA的翻译是通过一个不依赖于帽的机制发生的,该机制由来自5'非翻译区约450个核苷酸的区域指导,称为内部核糖体进入位点(IRES)。蛋白质合成的内部起始不需要任何病毒蛋白质。此外,当宿主细胞蛋白质合成几乎被废除时,它也能维持。通过使用体外翻译系统,已经定义了两个不同的IRES元件家族,它们具有非常不同的预测RNA二级结构。在兔网织细胞裂解液中,心脏病毒和阿佛罗病毒成分的作用非常有效,而肠道病毒和鼻病毒成分的作用则很差。然而,用额外的细胞蛋白补充这个翻译系统可以刺激肠病毒和鼻病毒rna指导的翻译,并减少异常起始产物的产生。与小核糖核酸病毒IRES相互作用的细胞蛋白的表征是研究的主要焦点。通过体外分析,例如紫外交联,可以观察到许多不同的蛋白质物种与IRES区域相互作用。然而,许多这些相互作用的功能和意义并不总是为人所知。对于两种蛋白,La和聚嘧啶束结合蛋白,已经获得了它们与IRES元素相互作用的功能作用的证据。
{"title":"RNA-protein interactions in regulation of picornavirus RNA translation.","authors":"G. Belsham, N. Sonenberg","doi":"10.1128/MMBR.60.3.499-511.1996","DOIUrl":"https://doi.org/10.1128/MMBR.60.3.499-511.1996","url":null,"abstract":"The translation of picornavirus RNA occurs by a cap-independent mechanism directed by a region of about 450 nucleotides from the 5' untranslated region, termed an internal ribosome entry site (IRES). Internal initiation of protein synthesis occurs without any requirement for viral proteins. Furthermore, it is maintained when host cell protein synthesis is almost abolished. By using in vitro translation systems, two distinct families of IRES elements which have very different predicted RNA secondary structures have been defined. The cardiovirus and aphthovirus elements function very efficiently in rabbit reticulocyte lysate, whereas the enterovirus and rhinovirus elements function poorly in this system. However, supplementation of this translation system with additional cellular proteins can stimulate translation directed by the enterovirus and rhinovirus RNAs and reduce production of aberrant initiation products. The characterization of cellular proteins interacting with the picornavirus IRES is a major focus of research. Many different protein species can be observed to interact with regions of the IRES by in vitro analyses, e.g., UV cross-linking. However, the function and significance of many of these interactions are not always known. For two proteins, La and the polypyrimidine tract-binding protein, evidence has been obtained for a functional role of their interaction with IRES elements.","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"25 1","pages":"499-511"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88343098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 279
RNA-protein interactions in regulation of picornavirus RNA translation. RNA-蛋白相互作用调控小核糖核酸翻译。
Pub Date : 1996-09-01 DOI: 10.1128/mr.60.3.499-511.1996
G J Belsham, N Sonenberg

The translation of picornavirus RNA occurs by a cap-independent mechanism directed by a region of about 450 nucleotides from the 5' untranslated region, termed an internal ribosome entry site (IRES). Internal initiation of protein synthesis occurs without any requirement for viral proteins. Furthermore, it is maintained when host cell protein synthesis is almost abolished. By using in vitro translation systems, two distinct families of IRES elements which have very different predicted RNA secondary structures have been defined. The cardiovirus and aphthovirus elements function very efficiently in rabbit reticulocyte lysate, whereas the enterovirus and rhinovirus elements function poorly in this system. However, supplementation of this translation system with additional cellular proteins can stimulate translation directed by the enterovirus and rhinovirus RNAs and reduce production of aberrant initiation products. The characterization of cellular proteins interacting with the picornavirus IRES is a major focus of research. Many different protein species can be observed to interact with regions of the IRES by in vitro analyses, e.g., UV cross-linking. However, the function and significance of many of these interactions are not always known. For two proteins, La and the polypyrimidine tract-binding protein, evidence has been obtained for a functional role of their interaction with IRES elements.

小核糖核酸RNA的翻译是通过一个不依赖于帽的机制发生的,该机制由来自5'非翻译区约450个核苷酸的区域指导,称为内部核糖体进入位点(IRES)。蛋白质合成的内部起始不需要任何病毒蛋白质。此外,当宿主细胞蛋白质合成几乎被废除时,它也能维持。通过使用体外翻译系统,已经定义了两个不同的IRES元件家族,它们具有非常不同的预测RNA二级结构。在兔网织细胞裂解液中,心脏病毒和阿佛罗病毒成分的作用非常有效,而肠道病毒和鼻病毒成分的作用则很差。然而,用额外的细胞蛋白补充这个翻译系统可以刺激肠病毒和鼻病毒rna指导的翻译,并减少异常起始产物的产生。与小核糖核酸病毒IRES相互作用的细胞蛋白的表征是研究的主要焦点。通过体外分析,例如紫外交联,可以观察到许多不同的蛋白质物种与IRES区域相互作用。然而,许多这些相互作用的功能和意义并不总是为人所知。对于两种蛋白,La和聚嘧啶束结合蛋白,已经获得了它们与IRES元素相互作用的功能作用的证据。
{"title":"RNA-protein interactions in regulation of picornavirus RNA translation.","authors":"G J Belsham,&nbsp;N Sonenberg","doi":"10.1128/mr.60.3.499-511.1996","DOIUrl":"https://doi.org/10.1128/mr.60.3.499-511.1996","url":null,"abstract":"<p><p>The translation of picornavirus RNA occurs by a cap-independent mechanism directed by a region of about 450 nucleotides from the 5' untranslated region, termed an internal ribosome entry site (IRES). Internal initiation of protein synthesis occurs without any requirement for viral proteins. Furthermore, it is maintained when host cell protein synthesis is almost abolished. By using in vitro translation systems, two distinct families of IRES elements which have very different predicted RNA secondary structures have been defined. The cardiovirus and aphthovirus elements function very efficiently in rabbit reticulocyte lysate, whereas the enterovirus and rhinovirus elements function poorly in this system. However, supplementation of this translation system with additional cellular proteins can stimulate translation directed by the enterovirus and rhinovirus RNAs and reduce production of aberrant initiation products. The characterization of cellular proteins interacting with the picornavirus IRES is a major focus of research. Many different protein species can be observed to interact with regions of the IRES by in vitro analyses, e.g., UV cross-linking. However, the function and significance of many of these interactions are not always known. For two proteins, La and the polypyrimidine tract-binding protein, evidence has been obtained for a functional role of their interaction with IRES elements.</p>","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"60 3","pages":"499-511"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC239454/pdf/600499.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19809133","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Microbial metabolism of pyridine, quinoline, acridine, and their derivatives under aerobic and anaerobic conditions. 吡啶、喹啉、吖啶及其衍生物在好氧和厌氧条件下的微生物代谢。
Pub Date : 1996-09-01 DOI: 10.1128/MMBR.60.3.483-498.1996
JEAN-PIERRE Kaiser, Yucheng Feng, J. Bollag
Our review of the metabolic pathways of pyridines and aza-arenes showed that biodegradation of heterocyclic aromatic compounds occurs under both aerobic and anaerobic conditions. Depending upon the environmental conditions, different types of bacteria, fungi, and enzymes are involved in the degradation process of these compounds. Our review indicated that different organisms are using different pathways to biotransform a substrate. Our review also showed that the transformation rate of the pyridine derivatives is dependent on the substituents. For example, pyridine carboxylic acids have the highest transformation rate followed by mono-hydroxypyridines, methylpyridines, aminopyridines, and halogenated pyridines. Through the isolation of metabolites, it was possible to demonstrate the mineralization pathway of various heterocyclic aromatic compounds. By using 14C-labeled substrates, it was possible to show that ring fission of a specific heterocyclic compound occurs at a specific position of the ring. Furthermore, many researchers have been able to isolate and characterize the microorganisms or even the enzymes involved in the transformation of these compounds or their derivatives. In studies involving 18O labeling as well as the use of cofactors and coenzymes, it was possible to prove that specific enzymes (e.g., mono- or dioxygenases) are involved in a particular degradation step. By using H2 18O, it could be shown that in certain transformation reactions, the oxygen was derived from water and that therefore these reactions might also occur under anaerobic conditions.
我们对吡啶和氮杂芳烃代谢途径的回顾表明,杂环芳烃的生物降解在好氧和厌氧条件下都发生。根据环境条件,不同类型的细菌、真菌和酶参与这些化合物的降解过程。我们的综述表明,不同的生物体使用不同的途径来生物转化底物。我们的回顾还表明,吡啶衍生物的转化速率依赖于取代基。例如,吡啶羧酸的转化率最高,其次是单羟基吡啶、甲基吡啶、氨基吡啶和卤代吡啶。通过代谢物的分离,可以证明各种杂环芳香族化合物的矿化途径。通过使用14c标记的底物,可以证明特定杂环化合物的环裂变发生在环的特定位置。此外,许多研究人员已经能够分离和表征参与这些化合物或其衍生物转化的微生物甚至酶。在涉及18O标记以及使用辅助因子和辅酶的研究中,有可能证明特定的酶(例如,单加氧酶或双加氧酶)参与特定的降解步骤。通过使用H2 18O,可以证明在某些转化反应中,氧来源于水,因此这些反应也可能在厌氧条件下发生。
{"title":"Microbial metabolism of pyridine, quinoline, acridine, and their derivatives under aerobic and anaerobic conditions.","authors":"JEAN-PIERRE Kaiser, Yucheng Feng, J. Bollag","doi":"10.1128/MMBR.60.3.483-498.1996","DOIUrl":"https://doi.org/10.1128/MMBR.60.3.483-498.1996","url":null,"abstract":"Our review of the metabolic pathways of pyridines and aza-arenes showed that biodegradation of heterocyclic aromatic compounds occurs under both aerobic and anaerobic conditions. Depending upon the environmental conditions, different types of bacteria, fungi, and enzymes are involved in the degradation process of these compounds. Our review indicated that different organisms are using different pathways to biotransform a substrate. Our review also showed that the transformation rate of the pyridine derivatives is dependent on the substituents. For example, pyridine carboxylic acids have the highest transformation rate followed by mono-hydroxypyridines, methylpyridines, aminopyridines, and halogenated pyridines. Through the isolation of metabolites, it was possible to demonstrate the mineralization pathway of various heterocyclic aromatic compounds. By using 14C-labeled substrates, it was possible to show that ring fission of a specific heterocyclic compound occurs at a specific position of the ring. Furthermore, many researchers have been able to isolate and characterize the microorganisms or even the enzymes involved in the transformation of these compounds or their derivatives. In studies involving 18O labeling as well as the use of cofactors and coenzymes, it was possible to prove that specific enzymes (e.g., mono- or dioxygenases) are involved in a particular degradation step. By using H2 18O, it could be shown that in certain transformation reactions, the oxygen was derived from water and that therefore these reactions might also occur under anaerobic conditions.","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"8 1","pages":"483-98"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84080590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 255
Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia. 囊性纤维化的微生物发病机制:粘液样铜绿假单胞菌和洋葱伯克氏菌。
Pub Date : 1996-09-01 DOI: 10.1128/mr.60.3.539-574.1996
J R Govan, V Deretic
Respiratory infections with Pseudomonas aeruginosa and Burkholderia cepacia play a major role in the pathogenesis of cystic fibrosis (CF). This review summarizes the latest advances in understanding host-pathogen interactions in CF with an emphasis on the role and control of conversion to mucoidy in P. aeruginosa, a phenomenon epitomizing the adaptation of this opportunistic pathogen to the chronic chourse of infection in CF, and on the innate resistance to antibiotics of B. cepacia, person-to-person spread, and sometimes rapidly fatal disease caused by this organism. While understanding the mechanism of conversion to mucoidy in P. aeruginosa has progressed to the point where this phenomenon has evolved into a model system for studying bacterial stress response in microbial pathogenesis, the more recent challenge with B. cepacia, which has emerged as a potent bona fide CF pathogen, is discussed in the context of clinical issues, taxonomy, transmission, and potential modes of pathogenicity.
铜绿假单胞菌和洋葱伯克霍尔德菌的呼吸道感染在囊性纤维化(CF)的发病机制中起主要作用。本文综述了CF中宿主-病原体相互作用的最新进展,重点介绍了铜绿假单胞菌(P. aeruginosa)向粘液样质的转化的作用和控制,这一现象体现了这种机会性病原体对CF慢性感染过程的适应,以及该菌对抗生素的先天耐药、人际传播和有时由该菌引起的快速致命疾病。虽然对P. aeruginosa向粘液样质的转化机制的理解已经取得了进展,这种现象已经演变为研究微生物发病机制中细菌应激反应的模型系统,但最近对洋葱芽孢杆菌的挑战已经成为一种有效的CF病原体,在临床问题,分类,传播和潜在的致病性模式的背景下进行了讨论。
{"title":"Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia.","authors":"J R Govan,&nbsp;V Deretic","doi":"10.1128/mr.60.3.539-574.1996","DOIUrl":"https://doi.org/10.1128/mr.60.3.539-574.1996","url":null,"abstract":"Respiratory infections with Pseudomonas aeruginosa and Burkholderia cepacia play a major role in the pathogenesis of cystic fibrosis (CF). This review summarizes the latest advances in understanding host-pathogen interactions in CF with an emphasis on the role and control of conversion to mucoidy in P. aeruginosa, a phenomenon epitomizing the adaptation of this opportunistic pathogen to the chronic chourse of infection in CF, and on the innate resistance to antibiotics of B. cepacia, person-to-person spread, and sometimes rapidly fatal disease caused by this organism. While understanding the mechanism of conversion to mucoidy in P. aeruginosa has progressed to the point where this phenomenon has evolved into a model system for studying bacterial stress response in microbial pathogenesis, the more recent challenge with B. cepacia, which has emerged as a potent bona fide CF pathogen, is discussed in the context of clinical issues, taxonomy, transmission, and potential modes of pathogenicity.","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"60 3","pages":"539-74"},"PeriodicalIF":0.0,"publicationDate":"1996-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC239456/pdf/600539.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19808433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 147
Artemisinin and the antimalarial endoperoxides: from herbal remedy to targeted chemotherapy. 青蒿素和抗疟内过氧化物:从草药到靶向化疗。
Pub Date : 1996-06-01 DOI: 10.1128/mr.60.2.301-315.1996
S R Meshnick, T E Taylor, S Kamchonwongpaisan

Artemisinin and its derivatives are endoperoxide-containing compounds which represent a promising new class of antimalarial drugs. In the presence of intraparasitic iron, these drugs are converted into free radicals and other electrophilic intermediates which then alkylate specific malaria target proteins. Combinations of available derivatives and other antimalarial agents show promise both as first-line agents and in the treatment of severe disease.

青蒿素及其衍生物是含有内过氧化物的化合物,是一类很有前途的新型抗疟药物。在寄生铁存在的情况下,这些药物被转化为自由基和其他亲电中间体,然后将特定的疟疾靶蛋白烷基化。现有衍生物和其他抗疟疾药物的组合,无论是作为一线药物还是治疗严重疾病,都显示出前景。
{"title":"Artemisinin and the antimalarial endoperoxides: from herbal remedy to targeted chemotherapy.","authors":"S R Meshnick,&nbsp;T E Taylor,&nbsp;S Kamchonwongpaisan","doi":"10.1128/mr.60.2.301-315.1996","DOIUrl":"https://doi.org/10.1128/mr.60.2.301-315.1996","url":null,"abstract":"<p><p>Artemisinin and its derivatives are endoperoxide-containing compounds which represent a promising new class of antimalarial drugs. In the presence of intraparasitic iron, these drugs are converted into free radicals and other electrophilic intermediates which then alkylate specific malaria target proteins. Combinations of available derivatives and other antimalarial agents show promise both as first-line agents and in the treatment of severe disease.</p>","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"60 2","pages":"301-15"},"PeriodicalIF":0.0,"publicationDate":"1996-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC239445/pdf/600301.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19772642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 41
Field evaluations of marine oil spill bioremediation. 海洋溢油生物修复的现场评价。
Pub Date : 1996-06-01 DOI: 10.1128/mr.60.2.342-365.1996
R P Swannell, K Lee, M McDonagh

Bioremediation is defined as the act of adding or improving the availability of materials (e.g., nutrients, microorganisms, or oxygen) to contaminated environments to cause an acceleration of natural biodegradative processes. The results of field experiments and trials following actual spill incidents have been reviewed to evaluate the feasibility of this approach as a treatment for oil contamination in the marine environment. The ubiquity of oil-degrading microorganisms in the marine environment is well established, and research has demonstrated the capability of the indigenous microflora to degrade many components of petroleum shortly after exposure. Studies have identified numerous factors which affect the natural biodegradation rates of oil, such as the origin and concentration of oil, the availability of oil-degrading microorganisms, nutrient concentrations, oxygen levels, climatic conditions, and sediment characteristics. Bioremediation strategies based on the application of fertilizers have been shown to stimulate the biodegradation rates of oil in aerobic intertidal sediments such as sand and cobble. The ratio of oil loading to nitrogen concentration within the interstitial water has been identified to be the principal controlling factor influencing the success of this bioremediation strategy. However, the need for the seeding of natural environments with hydrocarbon-degrading bacteria has not been clearly demonstrated under natural environmental conditions. It is suggested that bioremediation should now take its place among the many techniques available for the treatment of oil spills, although there is still a clear need to set operational limits for its use. On the basis of the available evidence, we have proposed preliminary operational guidelines for bioremediation on shoreline environments.

生物修复被定义为向污染环境中添加或提高物质(如营养物、微生物或氧气)的可用性,以加速自然生物降解过程的行为。对现场试验和实际泄漏事件后的试验结果进行了审查,以评价这种方法作为处理海洋环境中石油污染的可行性。海洋环境中普遍存在的石油降解微生物是公认的,研究表明,当地微生物群在接触石油后不久就能降解石油的许多成分。研究已经确定了许多影响石油自然生物降解率的因素,如石油的来源和浓度、石油降解微生物的可用性、营养物质浓度、氧气水平、气候条件和沉积物特征。以施肥为基础的生物修复策略已被证明可以促进好氧潮间带沉积物(如沙子和鹅卵石)中石油的生物降解率。间质水中含油量与氮浓度的比值是影响生物修复策略成功的主要控制因素。然而,在自然环境条件下,需要用碳氢化合物降解细菌播种还没有得到明确的证明。有人建议,生物补救现在应该在处理石油泄漏的许多现有技术中占有一席之地,尽管显然仍然需要为其使用设定操作限制。在现有证据的基础上,我们提出了岸线环境生物修复的初步操作指南。
{"title":"Field evaluations of marine oil spill bioremediation.","authors":"R P Swannell,&nbsp;K Lee,&nbsp;M McDonagh","doi":"10.1128/mr.60.2.342-365.1996","DOIUrl":"https://doi.org/10.1128/mr.60.2.342-365.1996","url":null,"abstract":"<p><p>Bioremediation is defined as the act of adding or improving the availability of materials (e.g., nutrients, microorganisms, or oxygen) to contaminated environments to cause an acceleration of natural biodegradative processes. The results of field experiments and trials following actual spill incidents have been reviewed to evaluate the feasibility of this approach as a treatment for oil contamination in the marine environment. The ubiquity of oil-degrading microorganisms in the marine environment is well established, and research has demonstrated the capability of the indigenous microflora to degrade many components of petroleum shortly after exposure. Studies have identified numerous factors which affect the natural biodegradation rates of oil, such as the origin and concentration of oil, the availability of oil-degrading microorganisms, nutrient concentrations, oxygen levels, climatic conditions, and sediment characteristics. Bioremediation strategies based on the application of fertilizers have been shown to stimulate the biodegradation rates of oil in aerobic intertidal sediments such as sand and cobble. The ratio of oil loading to nitrogen concentration within the interstitial water has been identified to be the principal controlling factor influencing the success of this bioremediation strategy. However, the need for the seeding of natural environments with hydrocarbon-degrading bacteria has not been clearly demonstrated under natural environmental conditions. It is suggested that bioremediation should now take its place among the many techniques available for the treatment of oil spills, although there is still a clear need to set operational limits for its use. On the basis of the available evidence, we have proposed preliminary operational guidelines for bioremediation on shoreline environments.</p>","PeriodicalId":18499,"journal":{"name":"Microbiological reviews","volume":"60 2","pages":"342-65"},"PeriodicalIF":0.0,"publicationDate":"1996-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC239447/pdf/600342.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19772643","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 64
期刊
Microbiological reviews
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1