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1.
Science ; 293(5530): 668-72, 2001 Jul 27.
Artigo em Inglês | MEDLINE | ID: mdl-11474104

RESUMO

The scarcity of usable nitrogen frequently limits plant growth. A tight metabolic association with rhizobial bacteria allows legumes to obtain nitrogen compounds by bacterial reduction of dinitrogen (N2) to ammonium (NH4+). We present here the annotated DNA sequence of the alpha-proteobacterium Sinorhizobium meliloti, the symbiont of alfalfa. The tripartite 6.7-megabase (Mb) genome comprises a 3.65-Mb chromosome, and 1.35-Mb pSymA and 1.68-Mb pSymB megaplasmids. Genome sequence analysis indicates that all three elements contribute, in varying degrees, to symbiosis and reveals how this genome may have emerged during evolution. The genome sequence will be useful in understanding the dynamics of interkingdom associations and of life in soil environments.


Assuntos
Genoma Bacteriano , Análise de Sequência de DNA , Sinorhizobium meliloti/genética , Simbiose/genética , Aderência Bacteriana , Proteínas de Bactérias/genética , Proteínas de Transporte/genética , Cromossomos Bacterianos/genética , Biologia Computacional , Elementos de DNA Transponíveis , Metabolismo Energético/genética , Evolução Molecular , Duplicação Gênica , Genes Bacterianos , Genes Essenciais , Genes Reguladores , Medicago sativa/microbiologia , Nitrogênio/metabolismo , Fixação de Nitrogênio/genética , Plasmídeos , Polissacarídeos Bacterianos/genética , Replicon , Rhizobiaceae/genética , Sinorhizobium meliloti/fisiologia
2.
DNA Seq ; 11(3-4): 207-10, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11092731

RESUMO

The Sinorhizobium meliloti genome consists of three replicons. This bacterium forms an intricate symbiotic relationship with the roots of certain legumes and is considered as an agriculturally important nitrogen-fixer. A consortium of 6 European laboratories was organized to sequence its single chromosome (3.7 Mb), whereas the other two elements (pSyma 1.4 Mb and pSymb 1.7 Mb) will be sequenced by other groups.


Assuntos
Cromossomos Bacterianos , Genoma Bacteriano , Sinorhizobium meliloti/genética , Sequência de Bases , Mapeamento Cromossômico , Cromossomos Artificiais Bacterianos , Mapeamento de Sequências Contíguas , Replicon
3.
Curr Microbiol ; 41(2): 109-13, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10856376

RESUMO

A high-resolution physical map of the larger megaplasmid (pSymb) of Sinorhizobium meliloti strain 1021 has been constructed by using BAC libraries and an original two-step PCR screening method. This method, previously used to map both the chromosome and the smaller megaplasmid (pSyma), allowed us to position over the genome a total of 842 markers with an average density of one marker every 8.3 kb. In addition, we used BLASTX and PRODOM analysis to predict a function for a number of STSs. This work led to the discovery of several interesting loci and to a comparison of the genetic information carried by each replicon. The two main results emerging from this study are (i) a biased distribution of housekeeping genes, mainly detected on chromosome, and (ii) the presence of an unexpected number of transporters, mainly belonging to the ABC superfamily. These are broadly distributed across the whole genome, but particularly found on pSymb.


Assuntos
Plasmídeos/genética , Replicon , Sinorhizobium meliloti/genética , Microbiologia do Solo , Transportadores de Cassetes de Ligação de ATP/genética , Genoma Bacteriano , Mapeamento Físico do Cromossomo , Raízes de Plantas/microbiologia
4.
Proc Natl Acad Sci U S A ; 96(16): 9357-62, 1999 Aug 03.
Artigo em Inglês | MEDLINE | ID: mdl-10430947

RESUMO

As part of the European Sinorhizobium meliloti (strain 1021) chromosome sequencing project, four genomic bacterial artificial chromosome (BAC) libraries have been constructed, one of which was mainly used for chromosome mapping. This library consists of 1,824 clones with an average insert size of 80 kilobases and represents approximately 20-fold total genome coverage [6.8 megabases (Mbs)]. PCR screening of 384 BAC clones with 447 chromosomal markers (PCR primer pairs), consisting of 73 markers representing 118 genes (40 individual genes and 78 genes clustered in 23 operons), two markers from the rrn operon (three loci), four markers from insertion sequences (approximately 16 loci) and 368 sequence-tagged sites allowed the identification of 252 chromosomal BAC clones and the construction of a high-density physical map of the whole 3.7-Mb chromosome of S. meliloti. An average of 5.5 overlapping and colinear BAC clones per marker, correlated with a low rate of deleted or rearranged clones (0.8%) indicate a solid BAC contigation and a correct mapping. Systematic BLASTX analysis of sequence-tagged site marker sequences allowed prediction of a biological function for a number of putative ORFs. Results are available at. This map, whose resolution averages one marker every 9 kilobases, should provide a valuable tool for further sequencing, functional analysis, and positional cloning.


Assuntos
Cromossomos Bacterianos/genética , Sinorhizobium meliloti/genética , Mapeamento Cromossômico , DNA Bacteriano/genética , Biblioteca Gênica , Genes Bacterianos , Marcadores Genéticos , Vetores Genéticos , Genoma Bacteriano , Reação em Cadeia da Polimerase
5.
Analyst ; 121(10): 1469-72, 1996 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8918219

RESUMO

An HPLC method has been developed for the determination of moxidectin in bovine tissues. The extraction and clean-up procedure is based on the matrix solid-phase dispersion technique. Control and moxidectin-fortified bovine tissue samples (0.25 g) are blended with octadecyl (C18 end-capped) packing material. A column made from the C18-bovine tissue blend is washed with hexane (2 ml); when all the hexane has eluted, an Alumina-B SPE cartridge is attached below the C18-tissue column and, after washing, moxidectin is eluted with methanol (6 ml). Moxidectin is derivatized and determined by HPLC with fluorescence detection. The recovery from fortified samples was greater than 80% in the concentration range 1-100 ng g-1 of tissue. This method permits the determination of moxidectin at levels as low as 1 ng g-1 (1 ppb).


Assuntos
Antibacterianos/análise , Animais , Bovinos , Cromatografia Líquida de Alta Pressão , Indicadores e Reagentes , Fígado/química , Macrolídeos/análise , Músculo Esquelético/química , Espectrometria de Fluorescência
6.
J Bacteriol ; 182(4): 1185-9, 2000 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10648551

RESUMO

To facilitate sequencing of the Sinorhizobium meliloti 1021 pSyma megaplasmid, a high-resolution map was constructed by ordering 113 overlapping bacterial artificial chromosome clones with 192 markers. The 157 anonymous sequence tagged site markers (81,072 bases) reveal hypothetical functions encoded by the replicon.


Assuntos
Mapeamento Físico do Cromossomo , Plasmídeos/genética , Sinorhizobium meliloti/genética , Cromossomos Bacterianos/genética , Sitios de Sequências Rotuladas
7.
Proc Natl Acad Sci U S A ; 98(17): 9877-82, 2001 Aug 14.
Artigo em Inglês | MEDLINE | ID: mdl-11481430

RESUMO

Sinorhizobium meliloti is an alpha-proteobacterium that forms agronomically important N(2)-fixing root nodules in legumes. We report here the complete sequence of the largest constituent of its genome, a 62.7% GC-rich 3,654,135-bp circular chromosome. Annotation allowed assignment of a function to 59% of the 3,341 predicted protein-coding ORFs, the rest exhibiting partial, weak, or no similarity with any known sequence. Unexpectedly, the level of reiteration within this replicon is low, with only two genes duplicated with more than 90% nucleotide sequence identity, transposon elements accounting for 2.2% of the sequence, and a few hundred short repeated palindromic motifs (RIME1, RIME2, and C) widespread over the chromosome. Three regions with a significantly lower GC content are most likely of external origin. Detailed annotation revealed that this replicon contains all housekeeping genes except two essential genes that are located on pSymB. Amino acid/peptide transport and degradation and sugar metabolism appear as two major features of the S. meliloti chromosome. The presence in this replicon of a large number of nucleotide cyclases with a peculiar structure, as well as of genes homologous to virulence determinants of animal and plant pathogens, opens perspectives in the study of this bacterium both as a free-living soil microorganism and as a plant symbiont.


Assuntos
Cromossomos Bacterianos/genética , Sinorhizobium meliloti/genética , Proteínas de Bactérias/genética , Proteínas de Transporte/genética , Divisão Celular/genética , Movimento Celular/genética , Cromossomos Artificiais Bacterianos/genética , Reparo do DNA/genética , Replicação do DNA/genética , DNA Bacteriano/genética , DNA Circular/genética , Metabolismo Energético/genética , Fabaceae/microbiologia , Duplicação Gênica , Genes Bacterianos , Dados de Sequência Molecular , Plantas Medicinais , Replicon/genética , Análise de Sequência de DNA , Transdução de Sinais/genética , Simbiose , Transcrição Gênica/genética , Virulência/genética
8.
Proc Natl Acad Sci U S A ; 98(17): 9883-8, 2001 Aug 14.
Artigo em Inglês | MEDLINE | ID: mdl-11481432

RESUMO

The symbiotic nitrogen-fixing soil bacterium Sinorhizobium meliloti contains three replicons: pSymA, pSymB, and the chromosome. We report here the complete 1,354,226-nt sequence of pSymA. In addition to a large fraction of the genes known to be specifically involved in symbiosis, pSymA contains genes likely to be involved in nitrogen and carbon metabolism, transport, stress, and resistance responses, and other functions that give S. meliloti an advantage in its specialized niche.


Assuntos
Plasmídeos/genética , Sinorhizobium meliloti/genética , Agrobacterium tumefaciens/genética , Aminoácidos/metabolismo , Proteínas de Ligação ao Cálcio/genética , Proteínas de Transporte/genética , DNA Bacteriano/genética , Células Eucarióticas/metabolismo , Regulação Bacteriana da Expressão Gênica/genética , Biblioteca Gênica , Genes Bacterianos , Dados de Sequência Molecular , Nitrogênio/metabolismo , Fixação de Nitrogênio/genética , Fenótipo , Replicon/genética , Análise de Sequência de DNA , Especificidade da Espécie , Transcrição Gênica/genética
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