Adaptations for insect‐trapping in brood‐site pollinated Colocasia (Araceae)

The Araceae include both taxa with rewarding and deceptive trap pollination systems. Here we report on a genus in which rewarding and imprisonment of the pollinators co‐occur. We studied the pollination of four species of Colocasia in Southwest China and investigated the morpho‐anatomical adaptations of the spathe related to the attraction and capture of pollinators. All four species were pollinated by drosophilid flies of the genus Colocasiomyia. The flies are temporally arrested within the inflorescence and departure is only possible after pollen release. Trapping of the flies is accomplished by the closure of the spathe during anthesis. Moreover, in two species the spathe is covered with papillate epidermal cells known to form slippery surfaces in deceptive traps of Araceae. However, in Colocasia the papillae proved not slippery for the flies. The morpho‐anatomical properties of the spathe epidermis indicate that it is an elaborate osmophore and serves for the emission of odours only. Despite its similarity to deceptive traps of other aroids, Colocasia and Colocasiomyia have a close symbiotic relationship, as the attracted flies use the inflorescence as a site for mating and breeding. The trap mechanism has presumably evolved independently in Colocasia and is supposed to facilitate more efficient pollen export.     

Therapeutic inducers of the HSP70/HSP110 protect mice against traumatic brain injury

Traumatic brain injury (TBI) induces severe harm and disability in many accident victims and combat‐related activities. The heat‐shock proteins Hsp70/Hsp110 protect cells against death and ischemic damage. In this study, we used mice deficient in Hsp110 or Hsp70 to examine their potential requirement following TBI. Data indicate that loss of Hsp110 or Hsp70 increases brain injury and death of neurons. One of the mechanisms underlying the increased cell death observed in the absence of Hsp110 and Hsp70 following TBI is the increased expression of reactive oxygen species‐induced p53 target genes Pig1, Pig8, and Pig12. To examine whether drugs that increase the levels of Hsp70/Hsp110 can protect cells against TBI, we subjected mice to TBI and administered Celastrol or BGP‐15. In contrast to Hsp110‐ or Hsp70i‐deficient mice that were not protected following TBI and Celastrol treatment, there was a significant improvement of wild‐type mice following administration of these drugs during the first week following TBI. In addition, assessment of neurological injury shows significant improvement in contextual and cued fear conditioning tests and beam balance in wild‐type mice that were treated with Celastrol or BGP‐15 following TBI compared to TBI‐treated mice. These studies indicate a significant role of Hsp70/Hsp110 in neuronal survival following TBI and the beneficial effects of Hsp70/Hsp110 inducers toward reducing the pathological consequences of TBI.

     

猕猴桃不同季节的嫁接法比较试验

在湖北的试验表明,猕猴桃春季嫁接以切接法较好,夏秋季嫁接则以单芽枝腹接法较好;嫁接后采用遮阳网遮荫可以显著提高嫁接成活率,但对出圃率无明显影响。     

Discontinuous DNA replication: accumulation of Simian virus 40 DNA at specific stages in its replication.

The number of proline residues in a protein should have very marked consequences for the rates of protein unfolding and refolding according to the model proposed by Brandts et al. (1975). Kinetic simulations of this model indicate that the half-time for refolding of a polypeptide chain with 20 proline residues should be greater than 10 minutes and should increase by about an order of magnitude for each additional 10 proline residues. Various means are considered by which the rate of protein folding in vivo and in vitro might be increased.     

微藻生物柴油研发态势分析

微藻是光合效率最高的原始植物之一,与农作物相比,单位面积的产率可高出数十倍。微藻生物柴油技术首先包括微藻的筛选和培育,获得性状优良的高含油量藻种,然后在光生物反应器中吸收阳光、CO2等,生成微藻生物质,最后经过采收、加工,转化为微藻生物柴油。完整的微藻生物柴油成套技术链涵盖多个技术环节,是一个复杂的系统工程,包括微藻生物工程技术、微藻高效规模化养殖技术,以及微藻生物质采收、加工与转化技术等。其中,降低生产成本是当前微藻生物柴油研究面临的主要挑战,各国的研究机构为此开展了多方面的研究。     

The role of DNA polymerase I-associated 5'-exonuclease in replication of coliphage M13 replicative-form DNA.

The conversion of both parental- and progeny-nascent open circular M13 RF DNA into covalently closed RF I is drastically reduced in an $\text{E. coli}$ mutant deficient in the 5′ → 3′ exonuclease associated with DNA polymerase I. The nascent progeny RF DNA also contains a significant proportion of fragments of smaller than unit length.     

Changes in Eucalyptus camaldulensis essential oil composition as response to drought preconditioning

Abstract

Water deficit, a common constraint in forestry, is the main cause of plant stress during plantation. The survival and growth of seedlings is also compromised by herbivory during establishment. The potential of nursery preconditioning to enhance survival chances of future trees by reducing palatability or attracting beneficial insects as a result of changes in chemical defences may be an answer to overcome this situation. Changes in essential oil production and composition were evaluated by GC and GC-MS in Eucalytus camaldulensis seedlings submitted to drought during four weeks at the last stage of nursery period (20 weeks). Significant changes in essential oil relative composition were found. Seedlings (young leaves) submitted to drought developed a terpenoid blend, which has been previously associated to mature leaves and related to their higher resistance towards herbivory. Total amount of non-oxygenated terpenes decreased by 44%, whereas some oxygenated sesquiterpenes (globulol, epiglobulol and ledol) were doubled, and 1,8-cineole content was enhanced by 28.3%.     

Cloning of the DNA repair genes mtcA, mtcB, uvsC, uvsD, uvsE and the leuB gene from Deinococcus radiodurans

A gene library from Deinococcus radiodurans has been constructed in the cosmid pJBFH. A 51.5-kb hybrid cosmid, pUE40, that transduced Escherichia coli HB101 from leucine dependence to independence was selected, and a 6.9-kb fragment which carried the leuB gene from D. radiodurans was subcloned into the EcoRI site of pAT153. The DNA repair genes mtcA, mtcB, uvsC, uvsD and uvsE, which code for two D. radiodurans UV endonucleases were identified by transforming appropriate repair-deficient mutants of D. radiodurans to repair proficiency with DNA derived from the gene library. Hybrid cosmid pUE50 (37.9 kb) containing an insert carrying both the mtcA and mtcB genes was selected and 5.6- and 2.7-kb DNA fragments carrying mtcA and mtcB, respectively, i.e., the genes that code for UV endonuclease alpha, were subcloned into the EcoRI site of pAT153. The three genes uvsC, uvsD and uvsE, that code for UV endonuclease beta, were all present in the 46.0-kb hybrid cosmid pUE60. The uvsE gene in a 12.2-kb fragment was subcloned into the HindIII site of pAT153 and the size of the insert reduced to 6.1 kb by deletion of a 6.7-kb fragment from the hybrid plasmid pUE62. None of the uvs genes introduced into the UV-sensitive E. coli CSR603 (uvrA-) was able to complement its repair defect. The mtcA, uvsC, uvsD and uvsE genes were found in the 52.5-kb hybrid cosmid pUE70. It is concluded that the DNA repair genes mtcA, mtcB, uvsC, uvsD and uvsE are located within an 83.0-kb fragment of the D. radiodurans genome.