Sucrose metabolism in Sorghum vulgare at ripening

Enzymes associated with sucrose metabolism in root, stem, leaf and grain of Sorghum vulgare Pers. (cv. JS 263) were studied at the ripening stage. Sucrose phosphate synthetase was dominating in the leaf and sucrose synthetase in the grain. Invertases were more active in leaf, root and stem tissues than in grains. The maximum activities of ADPG pyrophosphorylase and UDPG pyrophosphorylase were found in grains and leaves, respectively. Sucrose synthetase from grains catalyses both synthesis and cleavage of sucrose but the two activities differed in their responses to the effect of temperature, pH and type of buffer. The Km values of the enzyme for UDPG, ADPG, GDPG, TDPG and CDPG were 8.5, 5.3, 16.8 2.2 and 10.7 mM, and for UDP and ADP they were 17.2 and 55.0 mM respectively.     

Assessment of winter wheat cultivars for changes in straw composition and digestibility in response to fungicide and growth regulator treatments

The effects of a combined fungicide and growth regulator treatment on the composition and dry matter digestibility of straw samples of winter wheat cultivars, Beaver, Brigadier, Hussar, Mercia, Riband, Genesis, Hunter, Spark, Cadenza and Flame, were compared. The samples were analysed for nitrogen, ash, fibre fractions and minerals. Nitrogen content of treated samples was reduced compared to the untreated control samples and in contrast the proportion of ash increased for all the treated samples. All samples were analysed by derivative thermogravimetry (DTG) to determine changes in fibre composition. Only six cultivars were analysed by chemical fractionation methods to determine changes in lignin, cellulose and hemicellulose content. The results from the two methods of fibre analysis were broadly similar. K, Ca, Mg and Na concentrations of the treated straw samples were found to be different to the untreated samples. Increase in dry matter digestibility (DMD) of treated straw was observed for all cultivars; the effects on Beaver, Brigadier, Mercia, Riband, Genesis, Hunter and Cadenza were most pronounced, but were less for Hussar, Spark and Flame. The potential impact of these changes in straw quality on organic mushroom compost preparation is briefly discussed.     

Melanocortin Receptors: Identification and Characterization by Melanotropic Peptide Agonists and Antagonists

Hormones are chemical messengers released from cells to act on and control the activity of other cells. Hormonal ligands initiate their actions by interacting with receptive substances (Langley, 1906) of the target cells. These receptors are proteins that are either integral components of the cell membrane or are localized cytoplasmically within cells. Ligand-receptor interaction results in either the stimulation or inhibition of cellular activity. Since most hormones bind rather specifically to receptors possessed by their target cells, labeling of hormonal ligands can be utilized to identify and localize cells within an animal. In this report we discuss what is presently known about melanocortin receptors (MCRs) as studied by the use of labeled melanotropic peptide ligands.     

The Function of Urease in Citrullus Seeds

Urease is present in considerable quantity in the cotyledonsof Citrullus, though elsewhere in the plant it is present onlyin traces or is absent; urease activity in the cotyledons changesduring growth, showing an initial rise followed by an abruptdrop almost to zero. These changes, under a wide variety ofconditions, are not correlated with those in the major nitrogenfractions; they are, however, closely correlated with cell extensionand the associated changes in water content and respiration.A connexion with chlorophyll formation is possible but unlikely.It is suggested that the changes in cotyledonary urease constitutemerely one aspect of the ‘protoplasmic differentiation’that takes place as a cell matures.     

AGE-RELATED ALTERATIONS IN HUMAN CHROMOSOME COMPOSITION AND DNA CONTENT IN VITRO DURING SENESCENCE

Different theories of ageing involving somatic mutations, error catastrophe, compensation and repair, and programmed ageing were subjected to analysis for their feasibility from experimental data. Due to the relative difficulty of carrying out longitudinal studies in human subjects in vivo and the long periods involved, most of these experiments dealt with in vitro systems. I. Fibroblast cells in culture were found to be ideal materials for demonstrating senescence for a particular species and at the terminal end the cultures showed certain changes associated with age. II. It appears that the ideas regarding the alterations in DNA content at the terminal stages of the culture or otherwise are related to the tissues concerned and the duration of the cultured condition. III. The importance of DNA content specially related to the concept of stability of the DNA strand supports indirectly the error catastrophe theories. The rate of net DNA synthesis, the size of the replicon and duration of S phase is reported not to change during in vitro ageing. The regulation system of DNA replication may however change, but this alteration does not affect the DNA replication machinery. Following cell fusion studies it has been hypothesized that senescent human diploid fibroblasts contain a diffusible inhibitor which blocks cells at G₁ phase. Some immortal cell lines like HeLa and SV40-transformed cells would contain a dominant inducer that could override or inactivate the putative inhibitor, the nature of which is not yet clear. IV. DNA repair competence of fibroblast cultures is reported to decline near the end of in vitro life-span. However, it has been noted that the human skin fibroblasts from both young and old donors are equally proficient in repairing damage by UV light. V. The replication patterns of chromosomes from both senescent embryonic fibroblasts and early-passage adult skin fibroblasts were essentially identical. There were very few differences between the early-passage embryonic and adult skin cells. It was concluded that the terminal replication pattern of fibroblasts changes very little with cellular ageing. VI. A statistically significant increase in sister chromatid exchange frequency has been reported during the terminal part of fibroblast cultures. VII. Electron-microscopic studies have confirmed the increased organization of microfillaments into bundles in senescent cells. The presence of a rigid cytoskeletal structure may contribute in part to the inability of such cells to replicate. VIII. Age-related increase in nuclear proteins was attributed to accumulation of residual acid proteins. Densitometric analysis showed that histone HI was low in late-passage cells and H₄ fraction increased relatively at the terminal phase. IX. In contrast to age-matched controls, fibroblasts cultured from progeria and Werner's syndrome undergo significantly low population doubling. Metaphase plates from these patients demonstrated a much higher frequency of chromosomal abnor malities than normal fibroblasts. Frequency of sister chromatid exchange in cells from Fanconi's anaemia did not show any significant change as compared with control sets. X. Significantly lower Feulgen DNA values have been recorded from lymphocytes of the elderly as compared with younger ones, indicated by hypodiploidy as well as by the individual amounts of euchromatin and heterochromatin. However, later data from flow-cytometric measurements indicated that DNA content was the same for all age groups. XI. The UV-induced unscheduled DNA synthesis in lymphocytes of 80 to 90 year-old individuals was reduced as compared to younger persons. However, the rate of repair of DNA strand breaks is apparently constant in all the age groups. XII. Increase in aneuploidy from lymphocyte cultures of aged individuals has been recorded by many workers. XIII. Significantly lower titres of serine, threonine, histidine, ornithine and lysine have been observed in aged persons, and only the first three decreased equally in both sexes. Some of the amino acids were influenced by sex hormones. XIV. Study of the frequency of spontaneous sister chromatid exchanges showed that neither intra-individual variation between replicate cultures established from the same blood sample nor variation among samples from the same individual initiated at different times was significant. However, sensitivity to induced sister chromatid exchange is reported to increase with age.     

Production of polysaccharide-degrading enzymes by saprophytic fungi from glyphosate-treated flax and their involvement in retting

The fungi present on glyphosate-treated flax plants were isolated. Cladosporium herbarum, Epicoccum nigrum, Botrytis cinerea and yeasts occurred most frequently immediately after glyphosate treatment but as retting progressed the frequency of occurrence of Fusarium culmorum, Alternaria alternata and a Phoma sp. increased. Many of the fungi isolated from retting flax were also present as epiphytes on healthy flax stems. Glyphosate was shown to be fungitoxic in vitro but it had only a very slight effect on fungi colonising the flax. The application of sucrose and urea to flax 1 wk after glyphosate treatment resulted in more rapid fungal colonisation of the stems, but did not significantly enhance retting. When grown on sterilised flax stem sections, fungi known to be saprophytic on flax produced polysaccharide-degrading enzymes. All seven fungi tested produced polygalacturonase, pectin-lyase and xylanase. The greatest cellulase activity was present in stem tissues inoculated with F. culmorum and the Phoma sp. while no cellulase was detected in tissue inoculated with B. cinerea, a Mucor sp. or a Penicillium sp. Extracts from flax inoculated with the cellulolytic fungi caused the solubilisation of native cellulose. Pectinases, xylanase and cellulase were also detected in naturally-colonised senescing and dead flax stems. Stems which had been treated with a sucrose solution tended to contain the greatest enzyme activity.     

Limitations of Gas Exchanges in Intact Leaves during Ontogeny of Field-grown Chickpeas

The ontogenic changes in several component processes of photosynthesiswere measured in chickpeas. Gas exchange characteristics ofintact leaves were studied to analyse the effects of ambientconditions under which chickpeas are usually grown. The CO₂assimilation rate per unit leaf area remained fairly high duringthe vegetative stage, reaching a peak at early pod-fill anddeclining subsequently throughout pod development. The intercellularCO₂ partial pressure (C₁) remained more or less constant (195µbar) during vegetative growth and the early stages ofseed-filling. With falling RWC and PAR interception, the stomatalconductance declined more rapidly than the CO₂ assimilationrate resulting in a value of C₁ less than that normally existingunder ambient conditions. From the A/C₁-analysis, CO₂ assimilationduring pod-filling appears to be limited by the RuBP-regenerationcapacity because the carboxylation efficiency and in vitro RuBPCaseactivity were initially unaffected. However, as leaves aged,the carboxylation efficiency and in vitro RuBPCase activitydecreased abruptly with increasing leaf temperatures above 30°C, and the C₁ was greater than normally existing values(195 µbar), suggesting an increased mesophyll limitationof photosynthesis. It is suggested that a decline in the CO₂assimilation rate of leaves during pod development and an acceleratedsenescence are induced by adverse ambient conditions, particularlyplant water stress and high leaf temperature. Key words: Cicer arietinum L., gas exchange, photosynthesis, ribulose-1,5-bisphosphate carboxylase     

Witch Hunts, Herbal Healing, and Discourses of Indigenous Ecodevelopment in North India: Theory and Method in the Anthropology of Environmentality

ABSTRACT  In this article, we examine the environmental thought and practice of indigenous peoples living in and around a wildlife sanctuary in North India. Analysis reveals that those religious specialists (such as shamans) who possess knowledge of herbal healing are more committed than other villagers to preventing or mitigating the overharvesting of natural resources. To explain these results, reference is made to a specific juncture of native traditions and modern conditions and in particular to an intersection of local economies with global discourses of "ecodevelopment." Drawing on theories and methods from political ecology and cultural psychology, we present a framework for testing the extent that local actors—in this case, shamanic and herbalist healers—are differently positioned to resist or accommodate state and parastate structures of "environmentality" than are other villagers.     

Cytochemical Observations on Proteins,Alkaline and Acid Phosphatases,Adenosine Triphosphatase,and 5′-Nucleotidase in Chick Liver Cell Cultures Infected with Trichomonas vaginalis*, †

SYNOPSIS. By means of the ninhydrin-Schiff method for proteins a diffuse reaction as well as one localized in granular inclusions can be shown in the cytoplasm of fibroblasts, epithelial cells, and macrophages in trypsin-dispersed chick liver cell cultures. Nuclei and nucleoli also take the specific stain. A progressive loss of cytoplasmic and nuclear staining occurs in the fibroblasts in cultures infected with a relatively pathogenic strain of T. vaginalis. A loss occurs in epithelial cells in advanced stages of degeneration, but in less damaged cells, while the diffuse reaction disappears, the number and staining intensity of the cytoplasmic inclusions remain unchanged or possibly may increase somewhat. The intensity of the diffuse reaction and the number and size of the characteristic inclusions increase in the active, parasite-free, experimental macrophages, but phagocytes with trichomonads closely applied to their external surfaces and those containing the flagellates within their cytoplasm typically retain only a few weak-staining inclusions. Similar distribution of alkaline and acid phosphatases occurs in preparations treated according to Gomori's and Burstone's methods, except that no nuclear staining is obtained with the latter. Activity of both enzymes is localized primarily in inclusions which are dispersed thruout the cytoplasm of fibroblasts and epithelial cells and tend to accumulate along the cell membranes and around the nuclei. In the course of infection with T. vaginalis there is a progressive loss of alkaline phosphatase from both cell types; however, the acid phosphatase activity increases. In the control macrophages both enzymes are localized in mostly rather large, rounded cytoplasmic inclusions. The number of such inclusions increases in the parasite-free experimental macrophages, but only a few weak-staining granules remainin phagocytes with engulfed trichomonads and in those whose external surfaces are in direct contact with the parasites. The loss of the inclusions is less apparent in macrophages containing degenerated flagellates than in the ones with healthy trichomonads, but regardless of the condition of the parasites, the highest enzymatic activity is found around them. ATPase and 5′-nucleotidase are localized in small granules dispersed thruout the cytoplasm of fibroblasts and epithelial cells. The granules tend to accumulate along the periphery of the cells and around the nuclei. A diffuse cytoplasmic reaction is present in preparations processed for 5′-nucleotidase. Nuclei and nucleoli give positive reactions for both enzymes. In the course of infection with trichomonads, activity of the 2 enzymes declines in both culture cell types. Control macrophages have diffuse cytoplasmic reaction for ATPase and 5′-nucleotidase and these enzymes are localized also in rounded cytoplasmic inclusions. Activity of both enzymes increases in the parasite-free experimental phagocytes, but little if any diffuse staining and only a few characteristic inclusions are left in macrophages with engulfed healthy trichomonads and in those whose external surfaces are invested with the flagellates. The ninhydrin-Schiff-positive inclusions found in the macrophages appear to be the same as some of those which have acid phosphatase activity and may well be identical with the glycolipoprotein bodies noted by us previously. On the grounds of their chemical constitution and behavior it seems likely that the inclusions are lysosomes.     

Genetics of flowering time in bread wheat <Emphasis Type="Italic">Triticum aestivum</Emphasis>: complementary interaction between vernalization-insensitive and photoperiod-insensitive mutations imparts very early flowering habit to spring wheat

Time to flowering in the winter growth habit bread wheat is dependent on vernalization (exposure to cold conditions) and exposure to long days (photoperiod). Dominant Vrn-1 (Vrn-A1, Vrn-B1 and Vrn-D1) alleles are associated with vernalization independent spring growth habit. The semidominant Ppd-D1a mutation confers photoperiod-insensitivity or rapid flowering in wheat under short day and long day conditions. The objective of this study was to reveal the nature of interaction between Vrn-1 and Ppd-D1a mutations (active alleles of the respective genes vrn-1 and Ppd-D1b). Twelve Indian spring wheat cultivars and the spring wheat landrace Chinese Spring were characterized for their flowering times by seeding them every month for five years under natural field conditions in New Delhi. Near isogenic Vrn-1 Ppd-D1 and Vrn-1 Ppd-D1a lines constructed in two genetic backgrounds were also phenotyped for flowering time by seeding in two different seasons. The wheat lines of Vrn-A1a Vrn-B1 Vrn-D1 Ppd-D1a, Vrn-A1a Vrn-B1 Ppd-D1a and Vrn-A1a Vrn-D1 Ppd-D1a (or Vrn-1 Ppd-D1a) genotypes flowered several weeks earlier than that of Vrn-A1a Vrn-B1 Vrn-D1 Ppd-D1b, Vrn-A1b Ppd-D1b and Vrn-D1 Ppd-D1b (or Vrn-1 Ppd-D1b) genotypes. The flowering time phenotypes of the isogenic vernalization-insensitive lines confirmed that Ppd-D1a hastened flowering by several weeks. It was concluded that complementary interaction between Vrn-1 and Ppd-D1a active alleles imparted super/very-early flowering habit to spring wheats. The early and late flowering wheat varieties showed differences in flowering time between short day and long day conditions. The flowering time in Vrn-1 Ppd-D1a genotypes was hastened by higher temperatures under long day conditions. The ambient air temperature and photoperiod parameters for flowering in spring wheat were estimated at 25°C and 12 h, respectively.