Genetic Manipulation of Condensed Tannins in Higher Plants1 : II. Analysis of Birdsfoot Trefoil Plants Harboring Antisense Dihydroflavonol Reductase Constructs

We have produced and analyzed transgenic birdsfoot trefoil (Lotus corniculatus L.) plants harboring antisense dihydroflavonol reductase (AS-DFR) sequences. In initial experiments the effect of introducing three different antisense Antirrhinum majus L. DFR constructs into a single recipient genotype (S50) was assessed. There were no obvious effects on plant biomass, but levels of condensed tannins showed a statistical reduction in leaf, stem, and root tissues of some of the antisense lines. Transformation events were also found, which resulted in increased levels of condensed tannins. In subsequent experiments a detailed study of AS-DFR phenotypes was carried out in genotype S33 using pMAJ2 (an antisense construct comprising the 5′ half of the A. majus cDNA). In this case, reduced tannin levels were found in leaf and stem tissues and in juvenile shoot tissues. Analysis of soluble flavonoids and isoflavonoids in tannin down-regulated shoot tissues indicated few obvious default products. When two S33 AS-DFR lines were outcrossed, there was an underrepresentation of transgene sequences in progeny plants and no examples of inheritance of an antisense phenotype were observed. To our knowledge, this is the first report of the genetic manipulation of condensed tannin biosynthesis in higher plants.

Nodulating strains of Rhizobium loti arise through chromosomal symbiotic gene transfer in the environment.

Rhizobia were isolated from nodules off a stand of Lotus corniculatus established with a single inoculant strain, ICMP3153, 7 years earlier in an area devoid of naturalized Rhizobium loti. The isolates showed diversity in growth rate, Spe I fingerprint of genomic DNA, and hybridization pattern to genomic DNA probes. The 19% of isolates that grew at the same rate as strain ICMP3153 were the only isolates that had the same fingerprint as strain ICMP3153. Sequencing of part of the 16S rRNA gene of several diverse isolates confirmed that they were not derived from the inoculant strain. Nevertheless, all non-ICMP3153 strains gave EcoRI and Spe I hybridization patterns identical to ICMP3153 when hybridized to nodulation gene cosmids. Hybridization of digests generated by the very rare cutting enzyme Swa I revealed that the symbiotic DNA region (at least 105 kb) was chromosomally integrated in the strains. The results suggest that the diverse strains arose by transfer of chromosomal symbiotic genes from ICMP3153 to nonsymbiotic rhizobia in the environment.

Análisis de la captura incidental en la pesquería industrial de cerco anchovetera en el litoral peruano durante el período 2003-2011

En el Perú, la pesquería más importante está dirigida al recurso anchoveta (Engraulis ringens), el cual es extraído con red de cerco, sin embargo, este arte de pesca no es 100% selectivo, generando así capturas incidentales. Esta investigación tiene como objetivo analizar cuantitativamente el efecto de la pesquería de anchoveta sobre los recursos de la fauna acompañante mediante el estudio de diferencias espacio-temporales en términos de captura y composición específica de la ictiofauna que conformó la captura incidental en todo el litoral peruano proveniente de la flota industrial durante el periodo 2003-2011. Los resultados muestran valores de captura incidental significativamente mayores en la región sur del litoral peruano a comparación de la región norte y centro, principalmente durante los años 2003 y 2006, aunque la mayor riqueza de especies fue encontrada en la región norte. Por otro lado, dentro de la composición de la captura incidental a nivel especifico destacó la presencia constante de la Caballa (Scomber japonicus), Bagre (Galeichthys peruvianus) y Múnida (Pleuroncodes monodon) en la región norte, Lorna (Sciaena deliciosa), Pejerrey (Odontesthes regia regia), y Múnida (Pleuroncodes monodon) en la región centro y Jurel (Trachurus picturatus murphyi), Caballa (Scomber japonicus), Lorna (Sciaena deliciosa), Pejerrey (Odontesthes regia regia), Múnida (Pleuroncodes monodon), Camotillo (Diplectrum conceptione) y Pampanito (Trachinotus paitensis) en la región sur. Sin embargo, los mayores volúmenes capturados se debieron a recursos costeros y fueron capturados por la flota industrial de acero en la región sur del litoral peruano.