Aging and Mitochondrial Development in Potato Tuber Tissue

Respiratory activity of mitochondria isolated from fresh and aged potato tuber tissue has been determined. No significant change in activity of the particles (expressed per unit N) was observed as a result of aging. However, the yield of mitochondrial material increased with aging. It has been suggested that the commonly observed stimulation of respiration that accompanies aging of potato tissue can be attributed largely to an inerease in the mitochondrial population rather than to a stimulation of the particles per se, and that this increase results from a fission of pre-existing mitochondria. The respiratory activity of mitochondria isolated from unaged tissue was found to decline following storage of the tubers in the cold for extended periods. This decline was attributed to a loss of cristae structure in the particles, as observed microscopically. The possibility that this reduction in structural organization might be associated with changes in the state of dormancy of the tissue was considered.     

Plastid and Nuclear DNA in Potato Tuber Tissue 7

On exposure to light the outer parenchyma layers of mature potatobecame green as amyloplasts are converted to chloroamyloplasts.This tissue was sampled during greening, and analysed for nuclearand plastid DNA content. There was an increase in the proportionof plastid DNA in total DNA from 15% in white tuber tissue to22% in greened tissue, while the nuclear ploidy distributionand average nuclear ploidy was similar in both. Key words: Solatium tuberosum, greening, amyloplast     

Aging and the Development of Enhanced Respiration in Potato Tuber Tissue

Disks of potato tissue were aged by two separate methods. The resulting enhaiicetl respirations differed both qualitatively and quantitativety. It is suggested that the diverse results previously reported indicating changes in the terminal oxidative steps and/or in the relative contributions by competing metabolic pathways to the total respiration reflect variations in the methods employed to age the tissues. The nature of the stimulated respiration is discussed in terms of removal or retention of metabolites within the tissue during aging.     

The Effects of Pectic Enzymes and Phosphatidases on Potato Tuber Tissue

Extracts from rots of potato tubers caused by Erwinia atrosepticaand Corticium praticola were fractionated by precipitation withammonium sulphate and by gel filtration. For the various fractionsof the E. atroseptica extracts there was a close relation betweenthe activity of pectate franj-eliminase and capacity to increasethe permeability of protoplasts as assessed by loss of electrolytes.There was no such relation with phosphatidase acting on lecithin. For certain fractions of C. praticola extracts there was a similarclose relation between increase in permeability and activityof a polygalacturonase but for other fractions with low polygalacturonaseactivity there was a better relation with phosphatidase thoughall fractions that caused increase in permeability did havesome polygalacturonase activity. Phosphatidases which probablyplay no part in the killing of cells in E. atroseptica rotsmay, therefore, have some role in the killing of cells in C.praticola rots though they are likely to be less important thanpectic enzymes. Extracts from E. atroseptica rots caused marked increases inuptake of oxygen by tuber discs. Dialysis decreased and heatingeliminated this increase and had corresponding effects on permeability.However, after fractionation with ammonium sulphate, fractionswith high trans-eliminase activity had little effect on oxygenuptake whereas fractions with low trans-eliminase had littleeffect on permeability and greatly increased oxygen uptake. Similar results were obtained with C. praticola rot extracts.In contrast, nigericin and Triton X-100 both increased permeabilityand caused large increases in oxygen uptake The significance of these results is discussed especially inrelation to the killing of protoplasts by extracts from bothtypes of rot.     

Mechanism of the Increase in Ribonuclease Activity in Potato Tuber Slices

Upon wounding of potato tubers (Solanum tuberosum L. cv. Spunta)RNase activity increases, peaks in about 16 hours, then declines.To see if the increase of the activity is due to de novo synthesisof the enzyme protein, the extracts were compared for theirability to react with a rabbit antibody prepared against thewound activated RNase. The enzyme was purified by polyacrylamidegel electrophoresis of a RNase preparation, which had been partiallypurified from aged potato slices by ammonium sulfate precipitation,carboxymethyl-Sephadex column chromatography and gel filtrationthrough Sephadex G-100. Using rocket immunoelectrophoresis RNase-proteinimmunoprecipitated by the antibody increased in wounded tissue.This observation implies that the activity increase involvesenzyme synthesis. The increase was inhibited by actinomycinD and cordycepin, but not by 5-fluorouracil, suggesting a requirementfor mRNA synthesis. (Received April 9, 1985; Accepted December 16, 1985)     

Species-Specific Functions of Twinfilin in Actin Filament Depolymerization

Twinfilin is a highly conserved member of the actin depolymerization factor homology (ADF-H) protein superfamily, which also includes ADF/Cofilin, Abp1/Drebrin, GMF, and Coactosin. Twinfilin has a unique molecular architecture consisting of two ADF-H domains joined by a linker and followed by a C-terminal tail. Yeast Twinfilin, in conjunction with yeast cyclase-associated protein (Srv2/CAP), increases the rate of depolymerization at both the barbed and pointed ends of actin filaments. However, it has remained unclear whether these activities extend to Twinfilin homologs in other species. To address this, we purified the three mouse Twinfilin isoforms (mTwf1, mTwf2a, mTwf2b) and mouse CAP1, and used total internal reflection fluorescence microscopy assays to study their effects on filament disassembly. Our results show that all three mouse Twinfilin isoforms accelerate barbed end depolymerization similar to yeast Twinfilin, suggesting that this activity is evolutionarily conserved. In striking contrast, mouse Twinfilin isoforms and CAP1 failed to induce rapid pointed end depolymerization. Using chimeras, we show that the yeast-specific pointed end depolymerization activity is specified by the C-terminal ADF-H domain of yeast Twinfilin. In addition, Tropomyosin decoration of filaments failed to impede depolymerization by yeast and mouse Twinfilin and Srv2/CAP, but inhibited Cofilin severing. Together, our results indicate that Twinfilin has conserved functions in regulating barbed end dynamics, although its ability to drive rapid pointed end depolymerization appears to be species-specific. We discuss the implications of this work, including that pointed end depolymerization may be catalyzed by different ADF-H family members in different species.     

Enniatin Production by Fusarium Strains and Its Effect on Potato Tuber Tissue

Several Fusarium strains produce the cyclohexadepsipeptide enniatin, a host-nonspecific phytotoxin. Enniatins are synthesized by the 347-kDa multifunctional enzyme enniatin synthetase. In the present study, 36 Fusarium strains derived from a wide range of host plants were characterized with respect to enniatin production in different media. Thirteen of these strains produced enniatins on one or more of these media. To determine whether enniatin production affected virulence, an assay on potato tuber tissue was performed. Seven enniatin-producing and 16 nonproducing strains induced necrosis of potato tuber tissue, so that enniatin synthesis is not essential for the infection of potato tuber tissue. The application of a mixture of enniatins to slices of potato tuber, however, caused necrosis of the tissue. Therefore, enniatin production by the enniatin-synthesizing strains may affect their pathogenicity. The enniatin synthetase gene (esyn1) of Fusarium scirpi ETH 1536 was used as a probe to determine if similar sequences were present in the strains examined. In Southern blot analyses, DNA sequences hybridizing with the esyn1 probe were present in all but two of the strains examined. In some cases, enniatin-nonproducing strains had the same hybridization pattern as enniatin producers.     

Gibberellic Acid Activates Chromatin-bound DNA-dependent RNA Polymerase in Wounded Potato Tuber Tissue

Chromatin-bound DNA-dependent RNA polymerases react upon wounding of white potato tuber tissues with an increase in activity, which is additionally enhanced to 300% in the presence of 0.1 micromolar gibberellic acid (GA₃). 2,4-Dichlorophenoxyacetic acid is only weakly effective and indoleacetic acid not at all. Wounding and treatment with GA₃ affect template availability of chromatin only slightly. The hormone has no effect on chromatin-bound RNA polymerases, if added in vitro.     

Measuring the Deformation of Cells within a Piece of Compressed Potato Tuber Tissue

For the successful mathematical mechanical modelling of livingplant tissues, relationships between cellular deformations andtissue deformation need to be investigated. In previous workthese relationships have often been assumed. In this paper thedeformation of living cells within potato tuber tissue is measuredusing light microscopy and image analysis and is analysed inrelation to applied tissue deformations. The cell wall deformationwas found to depend upon the orientation of the cell wall faceswith respect to the global axes of the tissue and the appliedtissue deformation. Some faces experienced compression, whichreduced their surface area; others were deformed in bi-axialtension, thus increasing their surface area. These deformationswere successfully related to the global tissue deformations,using a simple constant volume affine deformation model, upto compressive deformations of 20% of specimen height. Somedeviation from the model was observed due to the bending ofcell walls in compression. Copyright 2000 Annals of Botany Company Potato tuber tissue, Solanum tuberosum, mechanical properties, cell walls, strain, re-orientation     

Stability of Polysome-Associated mRNA in Potato Tuber Cells during Aging of Tissue Discs

The stability of polysome-associated mRNA in potato tuber discsin the early stage of aging was examined by pulse-chase labelingexperiments and the change in the translational capacity ofthe RNA was studied using a wheat germ translation system. Theincorporation of pulse-fed ³H-uridine into polysomal RNA wasnot arrested immediately after the addition of actinomycin Dto the tissue, but increased by 25% during 4 hr of chasing.The radioactivity in the polysomal RNA then decreased by only30% of the value at the 4th hr during the next 9 hr in the presenceof actinomycin D. The remaining radioactivity in the polysomalRNA was stable at least for 18 hr. The proportion of radioactivityin polyadenylated RNA to that in non-polyadenylated RNA didnot vary appreciably during the chasing period. Non-polyadenylatedRNA of high molecular weight degraded faster than that of lowmolecular weight, but polyadenylated RNA did not show such size-selectivedegradation. The translational capacity of the polysomal RNAalso decreased by about 23% within 9 hr during the period ofinhibited RNA synthesis. In vivo experiments of ¹⁴C-leucineincorporation into proteins in the absence of RNA synthesissuggested that stable polysome-associated mRNA was actuallyfunctioning in the cells. SDS-polyacrylamide gel electrophoresisof the in vitro translation products indicated that mRNA codingfor polypeptides with relatively high molecular weights turnedover slightly faster than those for low molecular weight polypeptides. ¹Present address: Department of Agricultural Chemistry, Facultyof Horticulture, Chiba University, Matsudo 271, Japan. (Received May 12, 1982; Accepted August 26, 1982)     

Virulence and Enzyme Production of Erwinia carotovora ssp. atroseptica on Potato Tuber Tissue

The elicitation of pathogenesis on potato tuber slices by 6 strains of Erwinia carotovora ssp. atroseptica was investigated by neutral red vital staining and has been compared with bacterial growth rate, penetration ability, enzyme production and enzyme spectrum. The induction of enzyme synthesis (particularly, of the extracellular polygalacturonase) elicites the rot attack on tuber tissue and this requires a sufficient bacterial density. Due to wound healing, the inductors of enzyme production are removed, and after 48 h enzymes do not attack tuber tissue any more. Therefore, growth rate and penetration ability (to get the necessary bacterial density and inductor substances) may limit virulence. A similar influence of enzyme production and enzyme spectrum of the strains on the virulence was not detected.     

Pathogenesis of Potato Gangrene Caused by Phoma exigua var. foveata. I. Location of Phosphatase Activity in Diseased Tuber Tissue

The nitrocellulose blotting method was adapted for locating phosphatase activities in gangrene‐diseased tuber tissue. Adenine and glucose phosphates were used as enzyme substrates. A strong dephosphorylation of high‐energy phosphates took place in the UV‐fluorescent tissue adjacent to dry rots caused by Phoma exigua var. foveata, but the enzyme remained at a low activity in the other areas of the diseased tuber. Phosphatases were probably induced by P. exigua var. foveata, and intense dephosphorylation of high‐energy compounds leads to the death of potato tuber tissue.     

Biological Activity of Reducing-End-Derivatized Oligogalacturonides in Tobacco Tissue Cultures

The biological activity of reducing-end-modified oligogalacturonides was quantified in four tobacco (Nicotiana tabacum) tissue culture bioassays. The derivatives used were oligogalacturonides with the C-1 of their reducing end (a) covalently linked to a biotin hydrazide, (b) covalently linked to tyramine, (c) chemically reduced to a primary alcohol, or (d) enzymatically oxidized to a carboxylic acid. These derivatives were tested for their ability to (a) alter morphogenesis of N. tabacum cv Samsun thin cell-layer explants, (b) elicit extracellular alkalinization by suspension-cultured cv Samsun cells, (c) elicit extracellular alkalinization by suspension-cultured N. tabacum cv Xanthi cells, and (d) elicit H₂O₂ accumulation in the cv Xanthi cells. In all four bioassays, each of the derivatives had reduced biological activity compared with the corresponding underivatized oligogalacturonides, demonstrating that the reducing end is a key element for the recognition of oligogalacturonides in these systems. However, the degree of reduction in biological activity depends on the tissue culture system used and on the nature of the specific reducing-end modification. These results suggest that oligogalacturonides are perceived differently in each tissue culture system.