紫胶虫的有效性比

利用前人调查数据及近年研究结果,比较分析了几种紫胶虫的有效性比。结果表明,在同一种寄主植物上,相同的世代,不同年份间,田紫胶虫有效性比出现差异;相同年份、相同世代,在不同寄主植物上的田紫胶虫和紫胶蚧有效性比出现差异;在相同的寄主植物上,田紫胶虫和信德紫胶虫在一年中的2个不同世代的有效性比存在差异;对于同一种寄主植物,在相同年份的同一个世代,紫胶蚧和信德紫胶虫有效性比出现一定差异;在相同年份的同一个世代,不同种胶在相同寄主植物上,田紫胶虫的有效性比出现变化。环境温湿度和寄主植物的结构、营养和生长速度等对紫胶虫的有效性比可能产生影响。紫胶虫性比偏斜的机制可能同时遵循局域交配竞争和局域资源竞争。     

Olfactory responses of seed wasps Megastigmus pinus Parfitt and Megastigmus rafni Hoffmeyer (Hym., Torymidae) to host-tree odours and some monoterpenes

Megastigmus pinus and Megastigmus rafni are able to colonize the seed cones in eight different species of Abies in Denmark. Olfactory responses of M. pinus females from Abies alba and Abies procera seeds and of M. rafni females from A. alba and Abies grandis seeds to odours of different host-trees cones, needles and pure alpha-pinene and limonene were studied in a Y tube Plexiglas olfactometer. The odours of young cones significantly influenced the behaviour of females. The results obtained in experiments with cones from different trees indicate the occurrence of biotypes depending on the host tree within the M. pinus and M. rafni species. Megastigmus pinus females from A. procera cones preferred the cone odours of A. procera and were significantly repelled by the cone odours of other possible host trees. Megastigmus pinus females from A. alba cones preferred A. alba cone odour but were not indifferent to A. procera cones. This suggests that the M. pinus population in A. alba apparently originates from the A. procera population. Megastigmus rafni from A. grandis cones preferred only A. grandis cone odours. Megastigmus rafni females from A. alba cones preferred A. alba cone odour but were also significantly attracted by A. grandis cone odours. This probably indicates that the M. rafni population living in A. alba originates from the A. grandis population. Neither M. pinus nor M. rafni responded to the odours of the host-tree needles or alpha-pinene. The limonene odour significantly acted as a repellent to both seed chalcid species, independent of the origin-tree.     

紫胶蚧与寄主植物无机盐含量关系初步研究

采用比较研究法和聚类分析初步研究了紫胶蚧与7种寄主植物无机盐含量关系.结果表明,不同寄主植物之间和是否被紫胶蚧寄生的枝条之间,无机盐含量存在差异,14种枝条的无机盐含量分成4组.7种紫胶蚧寄主植物放虫枝条的无机盐含量经聚类分析可分成7类.寄主植物无机盐含量与紫胶蚧胶被厚、死亡率、怀卵量、个体泌胶量有一定关系,但不是很紧密.紫胶蚧寄生后久树枝条中氮、磷(P2O5)、铁都有不同程度的减少,钠元素含量几乎没有发生变化,钾、钙、镁、铜、锌、锰都有不同程度的增加,特别是钙元素含量,放虫枝条中钙元素的含量是未放虫枝条的5.3倍左右.其他寄主植物放虫枝条中都有不同种类元素不同程度地比未放虫枝条含量升高或降低.     

Disruption of LACCASE4 and 17 results in tissue-specific alterations to lignification of Arabidopsis thaliana stems

Peroxidases have been shown to be involved in the polymerization of lignin precursors, but it remains unclear whether laccases (EC 1.10.3.2) participate in constitutive lignification. We addressed this issue by studying laccase T-DNA insertion mutants in Arabidopsis thaliana. We identified two genes, LAC4 and LAC17, which are strongly expressed in stems. LAC17 was mainly expressed in the interfascicular fibers, whereas LAC4 was expressed in vascular bundles and interfascicular fibers. We produced two double mutants by crossing the LAC17 (lac17) mutant with two LAC4 mutants (lac4-1 and lac4-2). The single and double mutants grew normally in greenhouse conditions. The single mutants had moderately low lignin levels, whereas the stems of lac4-1 lac17 and lac4-2 lac17 mutants had lignin contents that were 20 and 40% lower than those of the control, respectively. These lower lignin levels resulted in higher saccharification yields. Thioacidolysis revealed that disrupting LAC17 principally affected the deposition of G lignin units in the interfascicular fibers and that complementation of lac17 with LAC17 restored a normal lignin profile. This study provides evidence that both LAC4 and LAC17 contribute to the constitutive lignification of Arabidopsis stems and that LAC17 is involved in the deposition of G lignin units in fibers.     

Evidence that selected amplification of a bacterial lac frameshift allele stimulates Lac(+) reversion (adaptive mutation) with or without general hypermutability

In the genetic system of Cairns and Foster, a nongrowing population of an E. coli lac frameshift mutant appears to specifically accumulate Lac(+) revertants when starved on medium including lactose (adaptive mutation). This behavior has been attributed to stress-induced general mutagenesis in a subpopulation of starved cells (the hypermutable state model). We have suggested that, on the contrary, stress has no direct effect on mutability but favors only growth of cells that amplify their leaky mutant lac region (the amplification mutagenesis model). Selection enhances reversion primarily by increasing the mutant lac copy number within each developing clone on the selection plate. The observed general mutagenesis is attributed to a side effect of growth with an amplification-induction of SOS by DNA fragments released from a tandem array of lac copies. Here we show that the S. enterica version of the Cairns system shows SOS-dependent general mutagenesis and behaves in every way like the original E. coli system. In both systems, lac revertants are mutagenized during selection. Eliminating the 35-fold increase in mutation rate reduces revertant number only 2- to 4-fold. This discrepancy is due to continued growth of amplification cells until some clones manage to revert without mutagenesis solely by increasing their lac copy number. Reversion in the absence of mutagenesis is still dependent on RecA function, as expected if it depends on lac amplification (a recombination-dependent process). These observations support the amplification mutagenesis model.     

Cytoplasmic fraction of Lactococcus lactis ssp. lactis induces apoptosis in SNU-1 stomach adenocarcinoma cells

Lactic acid bacteria are known to have antitumor activity, but the underlying mechanisms remain unclear. Recently we showed that a cytoplasmic fraction - but not peptidoglycan - of Lactococcus lactis ssp. lactis (L.lac CF) had strong antiproliferative activity on SNU-1 human stomach adenocarcinoma cells. The present study investigated whether the antiproliferative activity of L.lac CF on SNU-1 is linked to the induction of apoptosis. Treatment of L.lac CF inhibited the proliferation of SNU-1 cells in a dose- and time-dependent manner. Furthermore, treatment of the cells with 50 microg/ml and 100 microg/ml L.lac CF resulted in DNA fragmentation and chromatin condensation, respectively. The results indicate that the inhibitory effect of L.lac CF on SNU-1 cell growth is mainly attributable to the induction of apoptosis.     

Antimicrobial Efficacy of Methylated Lac Dye,an Anthraquinone Derivative

A natural red dye which is produced by the tiny insects Kerria lacca while feeding on host trees is popularly known as lac dye. Lac dye is a mixture of at least five closely related pure compounds all being anthraquinone derivatives designated as laccaic acid A, B, C, D and E. Anthraquinones isolated from different natural sources and reported to have potent antimicrobial activity. The lac dye, which is also a mixture of anthraquinone derivatives, is expected to exhibit antifungal and antibacterial activity. Lac dye cannot be used as antibacterial and antifungal agent due to its low water solubility and high polarity. Therefore, it is modified into its methyl derivative to enhance its bio-efficacy. Methylated lac dye is characterized with the help of TLC, UV–Vis spectroscopy and FT-IR, NMR analysis. An in vitro spore germination assay was carried out to evaluate the antifungal efficacy of methylated lac dye against some phytopathogenic fungi which commonly caused a various foliar diseases in crop plants viz., Alternaria solani, Curvularia lunata, Erysiphe pisi, Helminthosporium oryzae and Verticillium sp. Among the tested fungi, Verticillum sp. showed highest sensitivity, which showed 100% inhibition at 750 and 1000 µg/ml as compared to control. However, E. pisi an obligate parasite also showed varied sensitivity but at 1000 µg/ml showed 100% spore germination as compared to control. Methylated lac dye also showed strong antibacterial properties against Ralstonia solanacearum at very low concentration (40 and 50 µg/ml). Hence, lac dye may serve as potent antifungal and antibacterial agent in plant disease management.     

Enterotoxin B formation by fermentation mutants of Staphylococcus aureus.

An appreciable fraction of carbohydrate-negative (car) mutants of Staphylococcus aureus strains ATCC 14458, 778, and S-6 exhibit increased enterotoxin B (SEB) production. In addition, some lac and mtl mutants of these strains also display enhanced SEB formation. All such mutants appear to be point mutations. Mutagen-induced reversions of high SEB producing car, mtl, or lac mutants yield varying amounts of SEB and some clones seem to be restored to the characteristics of the parent type. A few sequentially isolated lac, mtl double mutants of strain 778 elaborate much more or much less SEB than either the lac or the mtl single mutants.     

Mutational analysis of an ssi region carried by plasmid pACYC184

To investigate the functional contribution of some structural components of the signal that directs single-stranded initiation of DNA replication (ssi signal) carried by a 119-nt segment of plasmid pACYC184 (Bahk et al., 1988), we constructed mutants carrying one-base substitutions and insertions using oligodeoxyribonucleotide (oligo) directed mutagenesis. Two one-base substitution mutants were obtained. The mutants, M13 delta lac 184/Sp and M13 delta lac 184/Ev, carried an SplI site and an EcoRV site, respectively, created by base substitution. Three kinds of synthetic oligos, that is, a 10-bp EcoRI linker, an 8-bp ScaI linker and an 8-bp SmaI linker, were inserted into the SplI site of M13 delta lac 184/Sp, and into the EcoRV site of M13 delta lac 184/Ev. The SSI activity of each mutant examined indicated that the one-base substitutions had different effects on the SSI functions of the altered ssi signals. This fact suggests that some structural components within the 119-bp region make distinct contributions to the SSI function. Moreover, when the three kinds of synthetic linkers were inserted into the mutants M13 delta lac 184/Sp and M13 delta lac 184/Ev, each of the insertion mutations affected the rate of conversion of ss DNA to RFI in vivo and the growth of the recombinant phages in a distinct manner. Judging from the above results, the base composition and the length of a certain specific site were crucial for maintenance of the SSI functional activity, and structural components of the ssi signal contributed distinctly to the SSI function.     

Kusum (Schleichera oleosa (Lour.) Oken): A potential multipurpose tree species,it's future perspective and the way forward

The species Schleichera oleosa (Kusum), being rich in nutritional, medicinal and processing qualities can play a very important role in the livelihood security of the rural communities through enhanced household income, employment generation and environmental protection. People of many states of India are becoming increasingly aware about the potential importance of this species in terms of its ethnobotany and lac production in their livelihood security. Value addition of all the components especially seed oil for biodiesel production, lac production and processing of bark for exploiting their nutritional and medicinal properties is a long-term strategy. There is need of increasing the area and plantation of this valuable species and enhancing their processed products. Moreover, to domesticate this species on farmer's field, there is a need to develop good cultivars. Hence, there is an ample scope in developing propagation methods and suitable good cultivars through nursery management programme. Dissemination of improved production technologies, value addition and marketing strategies regarding Kusum trees and its products to the farmers/entrepreneurs/lac based industries is of utmost importance for promoting it as agribusiness.     

Genetic variation within and among populations of Fomitopsis pinicola (Basidiomycetes)

RAPD polymorphisms were used to reveal the genetic population structure of Fomitopsis pinicola from 5 populations in southwestern Sweden with outliers in Finland and Norway. Eleven primers were used on 35 isolates. Using the Analysis of Molecular Variance (AMOVA), the total variance was divided into 3 hierarchical components: 84% within populations, 11% among regions, and 5% among populations within regions. The 3 large Swedish populations contained 95% of the variation within them. The statistical significance of these patterns was supported by permutation tests. The similarity index between all genets ranged from 0.10 to 0.72, with an average of 0.45. Genets from the same population could form more than one cluster in the neighbor-joining analysis. Some of these clusters were also supported by parsimony jack-knifing. This pattern is tentatively explained by establishment of spores from different basidiomata. The result of somatic incompatibility tests and RAPD markers were compared and this comparison indicated that compatible reactions do not necessarily imply genetic identity. Sampling from cut sections of infected trees revealed that multiple infections were present in a single tree and that the fungus probably infects host-trees by basidiospores, arriving via the air. Each somatically incompatible genet characteristically monopolized only part of a resource unit. Spore trapping showed no evidence of long distance spore dispersal, but this is probably due to the limited experiment, since the genetic analysis suggested a high rate of gene flow.     

The effect of genomic position on reversion of a lac frameshift mutation (lacIZ33) during non-lethal selection (adaptive mutation)

In a system described by Cairns and Foster, starvation of a particular leaky lac mutant (lacIZ33) in the presence of lactose appears to direct mutation in non-growing cells to sites that allow growth (adaptive mutation). This behaviour requires that the lac operon be located on an F' plasmid. This position effect was investigated by placing the mutant lac operon at many sites in the genome of Salmonella enterica (Typhimurium; LT2) and testing reversion behaviour. Genomic position did not affect reversion during non-selective growth. When lac was at any of 550 chromosomal sites, starvation caused little or no enhancement of reversion. In the 28 strains with the lac on Salmonella's conjugative plasmid (pSLT), selection enhanced reversion strongly, just as seen for strains with lac on an F' plasmid. In 46 strains, the lac operon was inserted within a small chromosomal duplication, and selection stimulated RecA-dependent partial reversion by simple amplification (about 8x) of the mutant lac region. The position of lac on a conjugative plasmid is important to reversion because it allows more frequent gene duplication and amplification. These events are central to growth and reversion under selection because they increase the number of replicating lac alleles within each developing revertant clone.     

Highly efficient production of laccase by the basidiomycete Pycnoporus cinnabarinus

An efficient transformation and expression system was developed for the industrially relevant basidiomycete Pycnoporus cinnabarinus. This was used to transform a laccase-deficient monokaryotic strain with the homologous lac1 laccase gene placed under the regulation of its own promoter or that of the SC3 hydrophobin gene or the glyceraldehyde-3-phosphate dehydrogenase (GPD) gene of Schizophyllum commune. SC3-driven expression resulted in a maximal laccase activity of 107 nkat ml(-1) in liquid shaken cultures. This value was about 1.4 and 1.6 times higher in the cases of the GPD and lac1 promoters, respectively. lac1-driven expression strongly increased when 25 g of ethanol liter(-1) was added to the medium. Accordingly, laccase activity increased to 1,223 nkat ml(-1). These findings agree with the fact that ethanol induces laccase gene expression in some fungi. Remarkably, lac1 mRNA accumulation and laccase activity also strongly increased in the presence of 25 g of ethanol liter(-1) when lac1 was expressed behind the SC3 or GPD promoter. In the latter case, a maximal laccase activity of 1,393 nkat ml(-1) (i.e., 360 mg liter(-1)) was obtained. Laccase production was further increased in transformants expressing lac1 behind its own promoter or that of GPD by growth in the presence of 40 g of ethanol liter(-1). In this case, maximal activities were 3,900 and 4,660 nkat ml(-1), respectively, corresponding to 1 and 1.2 g of laccase per liter and thus representing the highest laccase activities reported for recombinant fungal strains. These results suggest that P. cinnabarinus may be a host of choice for the production of other proteins as well.     

Nature of Lactose-fermenting Salmonella Strains Obtained from Clinical Sources

Six of seven lactose-fermenting (lac(+)) Salmonella strains obtained from clinical sources were found to be capable of transferring the lac(+) property by conjugation to Salmonella typhosa WR4204. All of the six S. typhosa strains which received the lac(+) property transferred it in turn to S. typhimurium WR5000 at the high frequencies typical of extrachromosomal F-merogenotes. These six lac elements were also transmissible from S. typhosa WR4204 to Proteus mirabilis and to some strains of Escherichia coli K-12; moreover, they were capable of promoting low frequency transfer of chromosomal genes from S. typhimurium WR5000 to S. typhosa WR4204. One of these lac elements was shown also to be capable of promoting low frequency chromosome transfer in E. coli K-12. E. coli K-12 strains harboring these lac elements exhibited sensitivity to the male specific phage R-17. Sensitivity to R-17 was not detected in Salmonella strains containing the elements. Examination of the lac elements in P. mirabilis by cesium chloride density gradient centrifugation showed that each element had a guanine plus cytosine content of 50%. The sizes of the elements varied from 0.8 to 3% of the total Proteus deoxyribonucleic acid. The amount of beta-galactosidase produced by induced and uninduced cultures of S. typhimurium WR5000 and S. typhosa WR4204 containing the lac elements was lower than that produced by these strains with the F-lac episome. The heat sensitivity of beta-galactosidase produced by the lac elements in their original Salmonella hosts indicated that the enzyme made by these strains differs from E. coli beta-galactosidase.     

Lichen diversity and composition in Araucaria forests and tree monocultures in southern Brazil

Tree plantations for commercial use have been replacing native ecosystems all over the world. We investigated how forest conversion to plantations of exotic and native tree species may influence lichen diversity and composition in a southern Brazilian landscape. The lichen community from the National Forest of São Francisco de Paula was studied using three stands of each of the four vegetation types: native Araucaria forest and plantations of Araucaria, Pine and Eucalyptus trees. All plantation stands were surrounded by native Araucaria forest, were of smaller size and were allowed to endure longer than commercially managed plantations. Lichen species and their cover abundance were recorded on tree trunks from 30 to 150 cm above soil level in ten host-trees that were randomly selected in each replication. Seventy-eight lichen species, from 18 genera and 9 families, were registered. Conversion of native forest to plantations of exotic tree species altered species composition by reducing the occurrence of shade tolerant lichens. Plantations of Araucaria angustifolia sustained the highest lichen diversity measured, because this is an excellent host species. These results suggest that a greater diversity of lichens can be preserved in the landscape, if plantations of the exotic Pinus and Eucalyptus genera are replaced by plantations of this native species.     

Asymmetry of frameshift mutagenesis during leading and lagging-strand replication in Escherichia coli

Mutations in DNA, including frameshifts, may arise during DNA replication as a result of mistakes made by the DNA polymerase in copying the DNA template strands. In our efforts to better understand the factors that contribute to the accuracy of DNA replication, we have investigated whether frameshift mutations on the Escherichia coli chromosome occur differentially within the leading and lagging-strands of replication. The experimental system involves measurement of the reversion frequency for several defined lac frameshift alleles in pairs of strains in which the lac target is oriented in the two possible directions relative to the origin of chromosomal replication. Within these pairs any defined lac sequence will be subject to leading-strand replication in one orientation and to lagging-strand replication in the other. Fidelity differences between the two modes of replication can be observed as a differential lac reversion between the two strains. Our results, obtained with a series of lac alleles in a mismatch-repair-defective background, indicate that for at least some of the alleles there is indeed a difference in the fidelity of replication between the two modes of replication.     

转基因林木潜在生态风险研究进展

近20年来,转基因技术在林木上的应用已使林木遗传育种研究取得了可喜的成绩,部分转基因林木已经进行了田间试验,还有一些获得了商品化许可。但与此同时,转基因林木的生态安全问题也逐渐引起了人们的关注,这些问题主要体现在外源基因的水平转移,垂直流动以及对昆虫、土壤生态系统、病毒等的潜在影响上。本文简要介绍了转基因林木田间试验、商品化生产情况及其潜在的生态风险,并对转基因林木的进一步发展进行了展望。     

In vitro and in vivo manipulations of bacteriophage Mu DNA: cloning of Mu ends and construction of mini-Mu's carrying selectable markers

Recombinant plasmids carrying one or both ends of the bacteriophage Mu genome were constructed by molecular cloning. Transposable mini-Mu's with selectable markers (ampicillin resistance, kanamycin resistance or the entire lac operon of Escherichia coli) inserted between the Mu ends were also constructed. As a source of lac operon DNA, a pBR322 derivative with a 27 kb insert containing the lac operon was constructed. The plasmids with both ends of Mu (mini-Mu's) conferred full Mu immunity upon the host cells. However, the same mini-Mu's containing kan or lac inserts were defective in immunity. A summary of the construction and physical characterization, including restriction endonuclease cleavage maps and some of the biological properties of the plasmids, is presented.