The pollen-collecting hairs of Campanula (Campanulaceae). I. Morphological variation and the retractive mechanism

The pollen-collecting hairs (PCHs) of Campanula have been a subject of intense debate for the past two centuries. Although several morphological studies have been made on these hairs, detailed comparative studies among species are still lacking, their function and adaptive significance being an unsolved question. The present study comprises two microscopy techniques: scanning electron microscopy and confocal scanning laser microscopy. The aim of the present study is to elucidate: 1) the variation in morphology of the PCHs, 2) the variation in presence/absence of the PCHs by the time of spreading of the stigmatic lobes, 3) the variation in the retractive mechanism of the PCHs, and 4) the correlation between pollination and the retraction of the PCHs. In several species PCHs of various lengths are found. Despite the variations in length of the hairs, the same retractive mechanism is found in all species studied. In most species the hairs retract into basal cavities within the style late in anthesis. The cells into which the hairs retract differ in length among species. Pollen grains are often found within the cavities together with the retracted hairs, a mechanism considered to prevent self-pollination. Pollen germination within the cavities was not observed. In a few species, the PCHs are still present at stigma receptivity. Differences in the shape and size of the cells surrounding the PCHs are documented. The diameter of the pits and the pollen grains vary among species. Other types of hairs on the style are recognized in some species, being of various lengths. These other types do not retract at stigma development and should not be regarded as pollen-collectors. They possibly facilitate for visiting insects to reach the nectar glands, present at the top of the ovary.     

Incorporation of arginine, ornithine and phenylalanine into tropane alkaloids in suspension-cultured cells and aseptic roots of intact plants oi Atropa belladonna

Label from U-¹⁴C-arginine (Arg), -ornithine (Orn) and -phenylalanine(Phe) was incorporated into hyoscyam-ine and scopolamine byboth dissected roots of intact plants and homogeneous or aggregatingsuspension cultures of Atropa belladonna L. The early biosyntheticcompounds (hygrine, tropinone, tropanol) were found only inthe roots, and alkaloid synthesis proceeded as far as to scopolaminethere. In the synthesis of the tropane skeleton, Orn was usedmore efficiently than Arg. Phe was quickly metabolized bothin roots and suspension cultures, and the label was incorporatedinto both ethanol-insoluble compounds, particularly proteinsand different ethanol-soluble compounds, especially phenolics. When the callus, used to initiate suspension cultures, was repeatedlysubcultured, the degree of organization of the suspension-culturedcells (second suspension passage) grown in the presence of 2.5µM 2-naphthaleneacetic acid (NAA), changed first fromhomogeneous to aggregating and later to heavily rooty. Simultaneouslywith an increasing degree of organization, alkaloid synthesisdecreased. At first, the rate of incorporation of Arg and Phe,and later Orn into alkaloids decreased. In heavily rooty suspensionsneither hyoscyamine nor scopolamine were found, but traces oftropanol were detected. Hence, the synthesis of tropane alkaloidsseems to be regulated at the later biosynthetic steps. Key words: Arginine, Atropa, hyoscyamine, omithine, phenylalanine, roots, scopolamine, suspension culture, tropane alkaloids     

Improved culture technique for strawberry (Fragaria × ananassa Duch.) protoplasts and the determination of DNA content in protoplast derived plants

A reproducible and efficient protoplast to plant-system has been developed for strawberry. By using young shoots growing on medium supplemented with cytokinin we were able to exclude the detrimental enzyme Pectolyase from our enzyme solution. The more gentle isolation procedure reported in this paper, together with the agarose-embedding system had a pronounced effect on protoplast viability and growth. Plant regeneration was enhanced by using thidiazuron instead of benzyladenine. Flow cytometric measurement of the DNA content in protoplast derived plants revealed that 27 out of 51 plants contained the amount of DNA corresponding to octoploid level. Fifteen plants exhibited chromosome doubling(16×), one was diplodecaploid(12×) and eight plants mixoploid.     

Macrocystis pyrifera in New Zealand: testing two mathematical models for whole plant growth

A Leslie-Lewis matrix projection model and a Markov chain model for whole plant growth in the giant Kelp,Macrocystis pyrifera, are developed and compared. Parameters of the models are estimated from field data gathered from several plants in New Zealand over a four-month period. Interpretations of the results are discussed.     

Nucleotide sequence of the structural gene for dUTPase of Escherichia coli K-12

The nucleotide sequence of the dUTPase structural gene, dut, of Escherichia coli has been determined. The DNA sequence predicts a polypeptide chain of 150 amino acid residues (mol. wt. 16 006) corresponding in size and composition to the purified dUTPase subunit. In a tentative promoter region preceding the dut gene, the -35 and -10 regions are separated by a SacI (SstI) site. Cloning of the dut gene utilization this SacI site was previously shown to reduce dut expression dramatically. The nucleotide sequence also contains a 210-codon open reading frame 106 bp downstream of dut and co-directional with dut. Previous protein synthesis experiments using dut plasmids allocated the gene of a polypeptide of mol. wt. 23 500 to this DNA region. The open reading frame thus may correspond to a protein of unknown function co-transcribed with the dut gene.     

Invasion of <Emphasis Type="Italic">Nipponaclerda biwakoensis</Emphasis> (Hemiptera: Aclerdidae) and <Emphasis Type="Italic">Phragmites australis</Emphasis> die-back in southern Louisiana,USA

Common reed, Phragmites australis (Cav.) Trin. Ex Steud., is the dominant emergent vegetation in the lower Mississippi River Delta (MRD), Louisiana, USA and is comprised primarily of introduced lineages of different phylogeographic origins. Dense stands of P. australis are important for protecting marsh soils from wave action and storm surges. In the Fall of 2016, while investigating symptoms of die-back of Phragmites stands in the lower marsh, a non-native scale was found infesting affected stands in high densities. Identified as Nipponaclerda biwakoensis (Kuwana) (Hemiptera: Aclerdidae), the scale was well established across the lower MRD. This report represents the first recorded population of Nipponaclerda biwakoensis in North America. Intriguingly, there are noticeable differences in die-back symptoms and in scale densities among different lineages of Phragmites in the MRD, with stands of the well-known European invasive lineage appearing healthier and having lower scale densities than other Phragmites lineages. Given its apparent relationship with the die-back syndrome, the scale may have serious implications for the health and stability of Phragmites marsh communities across coastal Louisiana. Efforts are currently underway to investigate the role of the scale and other abiotic stressors in the die-backs and potential management solutions.     

Amino acid sequence of human erythrocyte carbonic anhydrase C

Human carbonic anhydrase C is the high-specific-activity form of the enzyme found in human red cells. A proposal for the primary structure of this enzyme is presented. Trypsin-catalyzed hydrolysis was restricted to the arginyl bonds of the protein by blocking the lysyl side chains by amidination. The arginine fragments were isolated and their amino acid sequences determined. The sequence contains 259 amino acid residues in a single polypeptide chain devoid of disulfide bonds. The structure obtained should be adequate to permit a detailed interpretation of the 2.0 Å X-ray crystallographic model of the enzyme previously determined. The primary structures of the human B and C enzymes have about 60% identities.     

The Effect of Nonanal on Dipodascus aggregatus II. Influence of the Prehistory of the Inoculum and of the Presence of Ethanol

Nonanal, added in ethannlic solution, in concentrations lower than 40 to 80 μM did not affect the growth of Dipodascus aggregatus, provided the inoculum had been harvested from the exponential phase of growth. Growth could even be inhibited by 80 μM. If the inoculum had been grown to the exponential phase and then for another period, to the acceleration phase, in fresh liquid medium, growth was strongly promoted by 80 μM nonanal. If cells from the exponential phase were grown for another period in the supernatant fluid of centrifuged cultures from the exponential phase, 80 μM affected growth in the following way: in five different experiments growth was not stimulated, in one experiment undoubtedly promoted, and weakly stimulated in another one. The growth of cultures inoculated with cells grown only on malt agar was not affected by 80 μM nonanal. Pretreatment of cells, harvested from the acceleration phase, with nonanal (80 μM) in the presence of ethanol did not diminish the growth-promoting action of nonanal on the cultures inoculated with these cells. Nonanal, in the absence of ethanol, in a concentration of 10 μM did not affect the growth of cells, harvested from the acceleration phase, whereas 100 μM nonanal strongly inhibited growth. An attempt is made to explain the results starting from the endogenous metabolism.     

HSV‐1 ICP27 targets the TBK1‐activated STING signalsome to inhibit virus‐induced type I IFN expression

Herpes simplex virus (HSV) 1 stimulates type I IFN expression through the cGAS–STING–TBK1 signaling axis. Macrophages have recently been proposed to be an essential source of IFN during viral infection. However, it is not known how HSV‐1 inhibits IFN expression in this cell type. Here, we show that HSV‐1 inhibits type I IFN induction through the cGAS–STING–TBK1 pathway in human macrophages, in a manner dependent on the conserved herpesvirus protein ICP27. This viral protein was expressed de novo in macrophages with early nuclear localization followed by later translocation to the cytoplasm where ICP27 prevented activation of IRF3. ICP27 interacted with TBK1 and STING in a manner that was dependent on TBK1 activity and the RGG motif in ICP27. Thus, HSV‐1 inhibits expression of type I IFN in human macrophages through ICP27‐dependent targeting of the TBK1‐activated STING signalsome.