Iron metabolism in higher plants. The influence of nutrient iron on bean leaf lipoxygenase

Bean plants (Phaseolus vulgaris L.) were cultured in nutrient solutions containing three concentrations of iron. The leaves of plants grown with a limiting supply of iron contained reduced levels of protein, chlorophyll and the iron‐containing enzyme, lipoxygenase (EC 1.13.11.12). Measurements of lipoxygenase made on leaf crude extracts did not correlate with iron supply; however, upon purification of the enzyme by affinity chromatography, a direct correlation was observed. The lack of correlation was partly due to the presence of chlorophyll, an inhibitor of lipoxygenase, in the crude extract. Lipoxygenase levels changed with age of the plants, but rose to a maximum at days 14–16. A comparison of leaf lipoxygenases grown with different iron supply showed that they were identical with the same pH profile, chlorophyll inhibition, reaction products, and electrophoretic mobility. It is suggested that lipoxygenase may be used as a probe to evaluate iron availability and to investigate iron metabolism in higher plants.     

Yield and yield components of two irrigated red bean cultivars and some soil properties as influenced by wheat residues and nitrogen management

Crop residues are beneficial substances affecting crop production and soil properties. A field experiment was carried out to evaluate the effects of wheat (Triticum aestivum L.) residue rates (0, 25, 50 and 75%) combined with N levels (0, 34.5, 69, 103.5 kg ha^?1) on yield and yield components of two red common bean (Phaseolus vulgaris L.) cultivars and to monitor chemical soil parameters. The experiment was conducted at Research Center, College of Agriculture, Shiraz University, Shiraz, Iran for two years (2008–2009). The experiment was conducted as a split–split plot arranged in a randomized complete blocks design with three replications. The highest seed yield was obtained when 25–50% of residues were incorporated. The highest seed yield, seed weight per plant, 100-seed weight and seed number per pod were obtained with 103.5 kg N ha^?1 with no significant difference to 69 kg N ha^?1. Residue incorporation significantly increased soil organic carbon (SOC) as well as available K and P content. It is possible to sow red common bean as a double cropping by soil incorporation of 25–50% wheat residues with application of 69 kg N ha^?1.     

Synergistic effect of inoculating plant growth-promoting Pseudomonas spp. and Rhizobium leguminosarum-FB1 on growth and nutrient uptake of rajmash (Phaseolus vulgaris L.)

Plant growth-promoting bacteria (PGPB) Pseudomonas lurida-NPRp15 and Pseudomonas putida-PGRs4 possessing multiple plant growth-promoting traits were isolated from rhizoplane of pea and rhizosphere of garlic, respectively. The effects of individuals and combinations of Pseudomonas spp. with effective root nodulating symbiotic nitrogen fixing Rhizobium leguminosarum-FB1 on plant growth, nutrient uptake and yield of the rajmash plant were studied under greenhouse conditions. Bacterial inoculation resulted in significantly higher values for plant dry biomass, N, P, K, Zn and Fe contents as compared to the uninoculated control. Furthermore, dual inoculation of P. lurida-NPRp15 with R. leguminosarum-FB1 significantly increased root and shoot dry weight, nodulation, nutrient uptake, pod yield, and nutrient content of pods of rajmash VL63 compared to controls, single and triple inoculation. The results of the study indicate the potential of harnessing the benefit of plant growth-promoting and nitrogen-fixing microorganisms to improve the growth and yield of rajmash.     

Low root zone temperature effects on bean (Phaseolus vulgaris L.) plants inoculated with Rhizobium leguminosarum bv. phaseoli pre-incubated with methyl jasmonate and/or genistein

Abstract

Methyl jasmonate (MeJA) has recently been shown to act as a plant-to-bacteria signal. We tested the hypothesis that pre-induction of Rhizobium leguminosarum bv. phaseoli cells with genistein and/or MeJA would at least partially overcome the negative effects of low root zone temperature (RZT) on bean nodulation, nitrogen fixation and plant growth. Otebo bean plants were grown at constant air temperature (25^oC) and two RZT regimes (25 and 17^oC) and inoculated with R. leguminosarum bv. phaseoli pre-induced with MeJA and/or genistein. Our results indicate that low RZT inhibited nodulation, nitrogen fixation and plant growth. The plants growing at low RZT began fixing nitrogen seven days later compared to those at higher RZT. The low RZT plants had fewer nodules, lower nodule weight, less N fixation, slower plant growth, fewer leaves, smaller leaf area, and less dry matter accumulation comared to plants at a higher RZT. Rhzobium leguminosarum bv. phaseoli cells induced with genistein and/or MeJA enhanced bean nodulation, nitrogen fixation and growth at both optimum and suboptimum RZTs. The results of this study indicate that MeJA improves bean nitrogen fixation and growth at both optimum and suboptimum RZTs, and can be used alone or in combination with genistein to partially overcome the low RZT induced inhibitory effects on nodulation and nitrogen fixation.     

DRY BEAN GENOTYPES EVALUATION FOR GROWTH,YIELD COMPONENTS AND PHOSPHORUS USE EFFICIENCY

Dry bean along with rice is a staple food for the population of South America. In this tropical region beans are grown on Oxisols and phosphorus (P) is one of the most yield limiting factors for dry bean production on these soils. A greenhouse experiment was conducted to evaluate P use efficiency in 20 elite dry bean genotypes grown at deficient (25 mg P kg^?1 soil) and sufficient (200 mg P kg^?1) levels of soil P. Grain yields and yield components were significantly increased with P fertilization and, interspecific genotype differences were observed for yield and yield components. The grain yield efficiency index (GYEI) was having highly significant quadratic association with grain yield. Based on GYEI most P use efficient genotypes were CNFP 8000, CNFP 10035, CNFP10104, CNFC 10410, CNFC 9461, CNFC 10467, CNFP 10109 and CNFP 10076 and most inefficient genotypes were CNFC 10438, CNFP 10120, CNFP 10103, and CNFC 10444. Shoot dry weight, number of pods per plant, 100-grain weights and number of seeds per pod was having significant positive association with grain yield. Hence, grain yield of dry bean can be improved with the improvement of these plant traits by adopting appropriate management practices. Soil pH, extractable P and calcium (Ca) saturation were significantly influenced by P treatments. Based on regression equation, optimum pH value in water was 6.6, optimum P in Mehlich 1 extraction solution was 36 mg kg^?1 and optimum Ca saturation value was 37% for dry maximum bean yield.     

栽培甜菜和白花甜菜种间杂交后代无融合生殖的观察

栽培甜菜和白花甜菜杂交获得的Ｆ＿１代以栽培甜菜连续回交产生了Ｂ＿１Ｆ＿２代和Ｂ＿２Ｆ＿３代￣［４］．在Ｂ＿２Ｆ＿３代中，２ｎ＝２７的植株达３０．１９％，推测其中大多数染色体组仍为ＶＶＣ。具有ＶＶＣ染色体组的核型中，含９个白花甜菜校长的染色体和１８个较短的栽培甜菜染色体，差别明显，易于区分。我们通过对Ｂ＿１Ｆ＿２（Ｂ１４，２ｎ＝２７）和Ｂ＿２Ｆ－３（２ｎ＝２７）植株间形态特征相似性比较、两个世代植株有丝分裂特异核型比较、两类植株减粉分裂行为比较、过氧化物酶和酯酶同工酶酶谱相似性比较，有力地证明了栽培甜菜和白花甜菜种间杂交后代中，从Ｂ＿１Ｆ＿２（Ｂ１４）到Ｂ＿２Ｆ＿３之间传递上存在着无融合生殖现象。     

甜菜属种间杂交方法的研究

本文报道了甜菜属组间远缘种杂交困难的克服方法。观察到糖甜菜初级三体对B.corolliflora,B.Procumbens杂交的成功率为9％～41％,单体异附加系为12.5％～60％,说明远缘杂交中基因型构成有重要作用,三体及异附加系是良好的桥梁材料。发现B.vulgaris×B.patula→F_1,对前两个物种及B.Patellaris杂交成功率为20％～60％,说明它们不仅是良好的桥梁材料,而且所获三杂种材料可能具有重要的潜力。添加赤霉素、延迟及重复授粉只有辅助作用。生根素及受精胚珠培养是保证杂种存活的重要措施。     

GENETICALLY MODIFIED AND CONVENTIONAL DRY BEAN GENOTYPE RESPONSES TO SOIL FERTILITY

Dry bean is important pulse for the diet of South American population and results related to comparison of genetically modified and conventional dry bean genotypes to soil fertility are limited. A greenhouse experiment was conducted to compare genetically modified and conventional dry bean genotypes to soil fertility. Genotypes evaluated were Olathe Pinto, Olathe 5.1 (genetically modified), BRS Pontal, BRS Pontal 5.1 (genetically modified), Pérola and Pérola 5.1 (genetically modified). Fertility levels were 1 g fertilizer (5-30-15) kg^?1 soil (low fertility level) and 2 g fertilizer (5-30-15) per kg soil (high fertility level). These fertility levels were designated as low and high, respectively. Grain yield, number of pods per plants, and seed per pod were significantly increased with the increase in soil fertility. Shoot dry weight, seed per pod, and 100 seed weight were also significantly influenced by genotype treatment. Fertility X genotypes interaction was significant for maximum root length and root dry weight, indicating genotypes responded differently at two fertility levels in relations to these two traits. Shoot dry weight, number of pods per plant, and grain harvest index had significant association with grain yield, indicating that increase in these three traits grain yield can be increased. Grain yield efficiency index (GYEI) was having significant linear association with grain yield. Hence, on the basis of GYEI, genotypes were classified as efficient (E), moderately efficient (ME), and inefficient in nutrient use. Three conventional genotypes (Olathe Pinto, BRS Pontal and Pérola) and one genetically modified genotype (Olathe Pinto 5.1) were classified as moderately efficient and two genetically modified genotypes (Pérola 5.1 and BRS Pontal 5.1) were classified as efficient. None of the genotypes fall into the inefficient group.     

Identifying key components of weed beet management using sensitivity analyses of the GeneSys-Beet model in GM sugar beet

Genetically-modified (GM) sugar beet varieties tolerant to non-selective herbicides would be useful for managing weed beet, an annual form of Beta vulgaris impossible to eliminate with herbicides in sugar beet. However, it is highly probable that the herbicide-tolerance transgene would be transmitted to the weed through pollen flow. It is therefore essential to study how weed beet. particularly Herbicide-Tolerant (HT) populations, develop in cropping systems and how to optimise crop succession and management for controlling these weeds. As multiple interactions and long-term effects make field experiments impractical, we carried out a simulation study with a deterministic and mechanistic model, G ene S ys- B eet , which quantifies weed beet dynamics and gene flow in cropping systems with interactions with climate, soil structure and hydro-thermal conditions. The sensitivity analysis consisted of 250 000 random combinations of input variables to rank cropping system components according to their effect on both total and GM weed beet infestations. Frequency of sugar beet crops, crop succession, manual and mechanical weeding and tillage were identified as the most important variables. Several cultivation techniques must be combined to efficiently control weed beet. Our recommendations are complex, but a delayed return of sugar beet in the rotation. Harvest should be followed as soon as possible by a shallow tilling; tillage should always be as shallow and as early as possible, except before sugar beet where mouldboard ploughing is advisable. If possible, sowing dates should be delayed. Sugar beet should be weeded mechanically and/or manually, aiming at late and efficient, rather than early or frequent operations. Herbicides should be applied whenever possible and target all weed beet stages and genotypes. Set-aside must be cut as frequently and as late as possible.     

Development of STS markers and QTL validation for common bacterial blight resistance in common bean

Common bacterial blight (CBB) of common bean ( Phaseolus vulgaris L.), is one of the major diseases that decrease yield and quality. A major quantitative trait locus (QTL) for CBB resistance from line XAN 159 was transferred into two bean lines, HR45 and HR67. Previous studies identified that two markers are linked to this QTL but the chromosome location was not consistent. To identify more tightly linked markers and to verify the chromosome location, 65 additional markers were mapped using 81 recombinant inbred lines (RILs) derived from a cross HR67 × OAC95-4. The QTL was mapped to a 13 cM region on chromosome 1 and defined by eight molecular markers that explained 25–52% of the phenotypic variation. Six tightly linked amplified fragment length polymorphism markers (0.6–9.7 cM from the QTL peak) were converted into seven sequence tagged site markers, three of which were mapped to this QTL. Five tightly linked markers were used to screen 907 F₂ plants derived from a cross HR45 × 'OAC Rex' and four of them were linked to each other within 4.2 cM. These markers may be useful in marker-assisted selection and map-based cloning of this major QTL.