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Group II introns and expression of conjugative transfer functions in lactic acid bacteria

机译:二组乳酸菌中的缀合物转移功能的内含子和表达

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The homologous lactococcal conjugative elements pRSo1 and the sex factor of Lactococcus lactis strain 712 both contain a Group II intron within a gene believed to encode a conjugative relaxase enzyme. This enzyme is responsible for nicking of DNA at the origin of transfer (oriT) sequence of the sex factor DNA to initiate the strand transfer process. Group II introns have been studied in eukaryotes,and several of these elements in yeast mitochondrial genes have received considerable attention. These introns are relatively large in size and generally encode a protein withintheintron sequence. In addition to splicing activity, Group II introns are mobile genetic elements. The intronencoded proteins (IEPs) contain endonuclease and reverse transcriptase domains believed to play an enzymatic role in genetic mobility reactions, while a putative maturase domain is thought ot promote splicing by stabilizing the folding of the intron RNA into anactive ribozyme structure which carries out the splicing reaction. The lactococcal introns represent the first examples of Group II introns shown to be functional in vivo in prokaryotes. Because of the advantages of a bacterial system for genetic and molecular studies, the L1.1trB intron from pRSO1 has attracted the attention of several laboratories interested in Group II introns biology. Recently, it has been shown that the system can be adapted to function in Escherichia coli (although at somewhat reduced efficiency). In addition, it has been recently proven that the best studied form of mobility, the homing of the intron into an intronless allele of the cognate exon gene, occurs via an RNA intermediate and does not require DNA homology or generalized host recombination functions. The lactococcal Group II introns represent the first demonstrated genetically mobile prokaryotic retroelements, and they also have considerable potential as genetic engineering tools for Lactic Acid Bacteria (LAB) and other organisms.
机译:同源乳球菌缀合物的PRSO1和乳酸乳酸乳乳乳菌菌株712的性因子均含有在基因内的II族内含子,所述基因内被认为是编码缀合的酶酶的基因。该酶负责在性因子DNA的转移起源(ORIT)序列的起源中切断DNA,以引发链转移过程。 II族内含子在真核生物中研究,酵母线粒体基因中的几种元素受到相当大的关注。这些内含子的尺寸相对较大,并且通常以intinheIntron序列编码蛋白质。除拼接活性外,II组内含子是移动遗传元素。内核蛋白质(IEP)含有内切核酸酶和逆转录酶结构域,被认为在遗传迁移率反应中发挥酶促作用,而推定的熟化酶结构域是通过稳定内含子RNA的折叠成均匀的核酶结构来促进剪接。反应。乳球菌内含子代表II族内含子的第一个实施例,该内含子在原核生物中的体内具有功能性。由于遗传和分子研究的细菌系统的优点,PRSO1的L1.1TRB内含子引起了对II族内含子生物学感兴趣的几个实验室的注意。最近,已经表明该系统可以适于在大肠杆菌中的功能(虽然效率有点降低)。此外,最近证明了最佳研究的迁移率,内含子归巢到同源外显子基因的内部等位基因中,通过RNA中间体发生,并且不需要DNA同源性或广义主体重组功能。乳酰基核科学II内含子代表首先证明的遗传流动原核逆势,并且它们也具有相当大的潜力作为乳酸菌(实验室)和其他生物的基因工程工具。

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