SYMBIOTIC NITROGEN FIXATION IN CEANOTHUS ROOTS

Ceanothus greggii var. perplexans is a common shrub in the southern California chaparral. Clusters of nodules found under the canopy of this species are modified roots which contain a nitrogen-fixing endophyte, Frankia ceanothi (Actinomycetales), within the cortex. The nodule density per m² obtained from root system excavations is much lower than that reported for different Ceanothus species in northern California. Field observations indicate that soil moisture is an important factor in nodule formation. Anatomical studies with the scanning electron microscope and acetylene reduction assays support the hypothesis that the vesicles, spherical swellings of hyphal endings (1.2–3.0 μm in diam), are indeed the sites of N₂ fixation. No bacteria-like bodies were found. The acetylene reduction rates of C. greggii endophytes were of the same order of magnitude as those reported for other members of the genus Frankia. It is estimated that 100 grams of nitrogen are fixed per year per hectare for a specific area in the southern Californian chaparral where C. greggii comprises 1/3 of the ground cover. This amount appears to be large enough to replace the nitrogen that is lost annually by drainage and runoff from winter rain storms.     

CARBON DIOXIDE FIXATION IN BACILLUS ANTHRACIS

Eastin, Jerry D. (U.S. Army Chemical Corps, Frederick, Md.) and Curtis B. Thorne. Carbon dioxide fixation in Bacillus anthracis J. Bacteriol. 85:410-417. 1963.-Virulent strains of Bacillus anthracis require a concentration of CO(2) greater than that of the normal atmosphere (air) for the production of capsular material (glutamyl polypeptide); avirulent strains may produce no polypeptide or may produce polypeptide in air. Fixation of C(14)O(2) by each of the three types tested resulted in labeling of aspartic acid, glycine, glutamic acid, succinic acid, and an unidentified organic acid. C(14) was detected in aspartic acid after less than 30 sec of exposure of cells to C(14)O(2). Subsequent flushing of the cells with C(12)O(2) displaced C(14) from aspartic acid but not from the other labeled intermediates. Aspartic acid appears to be closely associated with the primary CO(2)-fixation product, and the data suggest a fairly direct carbon pathway from CO(2) to aspartic acid (oxaloacetic acid) to glutamic acid to glutamyl polypeptide.     

CARBON FIXATION IN CULTURED MARINE BENTHIC DIATOMS1

The enzyme activity of ribulose 1, 5-bisphosphate carboxylase-oxygenase (RuBisCO) and phosphoenolpyruvate carboxylase (PEPC) was measured in four species of marine benthic diatoms isolated from subtidal sediments of Graveline Bayou, Mississippi. Enzyme activities were measured in cultures of Amphora micrometra Giffen, A. tenerrima Aleem and Hustedt, Nitzschia fontifuga Cholnoky, and Nitzschia vermicularis Grunow that were grown at light levels supporting μ_max and at light-limiting irradiances. All four species exhibited similar RuBisCO: PEP ratios (range = 1–1.8) at μ_max the lowest ratio (0.4) was observed in A. micrometra. Reduced light levels increased PEPC relative to that measured at μ_max in two species. Two-dimensional paper chromatography was used to determine the first products of carbon fixation in A. micrometra After a 15 s incorporation period, the first product of photosynthetic carbon fixation was 3-phosphoglycerate even though this alga had a PEPC activity that was three times higher than that of RuBisCO. After 30 s, over 50% of the recovered radioactivity was still in this compound. Stable carbon isotope analyses of a mixture of the four pennate diatoms also suggest the predominant carbon fixation pathway in these benthic diatoms was similar to C3 plants.     

CARBONIC ANHYDRASE AND CARBON FIXATION IN COCCOLITHOPHORIDS1

Rates of carbon fixation in coccolithophorids in culture, unlike many other algae, are carbon limited at ambient levels of dissolved inorganic carbon (DIC). Apparently, plants often rely on activity of carbonic anhydrase (CA) to raise the level of CO₂ in cells and achieve carbon saturation. However, CA activities in the coccolithophorids, Coccolithus (= Emiliania) huxleyi Lohmann and Hymenomonas (=Cricosphaera) carterae Braarud, were either not detectable or very low compared to activities in other systems, including other algae, higher plants, and representative animals. Furthermore, additions of CA to medium with 2 mM DIC at pH 8.1 resulted in nearly 30% enhancement of photosynthesis, but not coccolith formation. Although carbon fixation in coccolithophorids can be suppressed by the CA inhibitor acetazolamide, studies of CaCO₃ nucleation revealed a non-specific effect of the inhibitor. Using a 30 min assay based on pH decreases accompanying loss of dissolved. CO₃^2-, inhibition of crystal formation in the absence of CA at 1 mM acetazolamide was demonstrated for decalcified crab carapace, a tissue with which normal CaCo₃ deposition in vitro has been shown. The results suggest only a minor role for CA in coccolithophorids.     

广东山区的兰科植物及其分布

通过野外调查和广泛收集前人的研究资料,概述了广东山区兰科植物的区系组成特点,分布区类型,水平分布,垂直分布,不同基质上分布的特点和分布格局的形成,文末附有广东山区兰科植物名录。     

SEASONAL PATTERNS OF PHOTOSYNTHESIS AND LIGHT-INDEPENDENT CARBON FIXATION IN MARINE MACROPHYTES1

The contribution of light-independent carbon fixation (LICF) to the overall carbon gain and the seasonal patterns of maximum photosynthesis (P_max and LICF were characterized in a broad taxonomic range of macrophytes from Monterey Bay, California. P_max and LICF rates (nmol C.g filtered seawater^?1.min^?1) varied among species and taxonomic groups examined, and as a function of tissue type in the phaeophyte Laminaria setchellii Silva (Phaeophyceae). On average, P_max values were higher in the Rhodophyta, whereas LICF rates were greater in the Phaeophyceae. LICF rates were generally less than 5% of P_max in the marine macrophytes studied and, as a consequence, cannot fully compensate for respiratory carbon losses, which usually are greater than 10% of P_max. All species studied possessed the highest P_max and LICF rates when irradiance levels were highest and decreased during periods of low incident irradiance. Seasonal patterns of P_max and LICF in most of the macrophytes from the stenothermal environment of Monterey Bay were strongly correlated with photosynthetic photon flux rather than seawater temperature. The concomitant decrease of LICF and P_max rates in all species examined argues against LICF playing a major role in carbon acquisition under light-limiting conditions as suggested previously. Rather, the strong positive correlation of P_max and LICF indicates the direct coupling of photosynthate (e.g. 3-phosphoglyceric acid) generation with production of substrates for LICF reactions. Our results also suggest that LICF might be a useful indicator of photosynthetic metabolism in marine macrophytes.     

NON-PHOTOSYNTHETIC FIXATION OF CARBON DIOXIDE AND POSSIBLE BIOLOGICAL ROLES IN HIGHER PLANTS

1. Non-photosynthetic fixation of CO₂/HCO₃^- occurs both under light and dark conditions and involve the addition of carbon to substrates which in higher plants are derived originally from carbon reduced to carbohydrates during photosynthesis. Despite the endergonic nature of these carboxylations, the advantages offered seem to be sufficient to outweigh the disadvantages of energy loss. 2. Non-photosynthetic carbon incorporation into metabolism is dealt mainly in relation to PEP carboxylase, acetyl-CoA carboxylase, carbamoyl phosphate synthetase and phosphoribosylaminoimidazole carboxylase while other carboxylases await further characterization or discovery. The extent to which a carboxylase participates depends upon the need for products of its activity in metabolism. 3. Non-photosynthetic carbon fixation is intricately involved in several pathways of metabolism throughout the ontogeny of plants. The roles in relation to leaf carbon metabolism, respiratory metabolism, nitrogen metabolism, lipid and isoprenoid biosynthesis, purine and pyrimidine metabolism and metabolism associated with the action of growth regulators have been described. The fixation reactions appear to be largely concerned with the production of intermediary metabolites, circumvention of energy barriers in metabolism and regulation of plant metabolism. In addition, the activity of PEP carboxylase is involved in ionic balance and pH-stat. 4. Malate derived by way of PEP carboxylase and NAD-malate dehydrogenase acts as an effective osmoticum and a counter-ion for K⁺ accumulation in actively growing plant cells. In addition, malate may enter the TCA cycle or can be decarboxylated by cytoplasmic NADP-malic enzyme converting NADH to NADPH. Wherever it has been sought in different plant tissues, some evidence for PEP carboxylase and metabolism of malate has always been found. 5. Almost every plant process spanning from seed development and germination to flowering and fruit-set requires the essential participation of non-photosynthetic carbon fixation in regulating certain metabolic and cellular functions but it does not contribute in a major way to the carbon nutrition of plants. It is largely the tissue type that appears to determine which of the roles is predominant at any one time.     

AN ORCHID SURVEY IN CONGO

Summary. An orchid survey to the Mayombe forest region of the Congo Republic is described; 100 orchid collections were made, mostly epiphytes and representing at least 22 genera, many of them new records for the area.     

AN EXPERIMENTAL SEPARATION OF OXYGEN LIBERATION FROM CARBON DIOXIDE FIXATION IN PHOTOSYNTHESIS BY CHLORELLA

Using intact cells of Chlorella pyrenoidosa it is possible to obtain oxygen by the reduction of certain reducible materials other than carbon dioxide. Of these, benzaldehyde was studied in some detail. This reduction does not involve the production of carbon dioxide from the benzaldehyde. Stoichiometrical relationships as expressed by the following equation: 2C₆H₅CHO + 2H₂O → 2C₆H₅CH₂OH + O₂ are somewhat difficult to obtain because the benzaldehyde can disappear from the reaction mixtures by dark reactions. The technique is now available which permits detailed studies of the oxygen-liberating mechanisms in photosynthesis.     

LIGHT INDEPENDENT CARBON FIXATION BY MARINE MACROALGAE1

Several marine macroalgae representative of the Chlorophyceae, Rhodophyceae and Phaeophyceae were investigated for their potentials of photosynthesis and light independent (dark) carbon fixation. In addition, the activities of ribulose-1,5-bisphosphate carboxylase (RubP-C; EC 4.1.1.39) and of phosphoenolpyruvate carboxykinase (PEP-CK; EC 4.1.1.32) were studied. In contrast to the green and red algae investigated, all brown algae exhibited comparably high rates of dark fixation accounting for up to 20% of photosynthetic carbon uptake. These observations are confirmed by the activities of RubP-C and PEP-CK measured after extraction from different species and thallus regions. Dark fixed ¹⁴C was mainly recovered from aspartate, citrate, malate, glutamate, and alanine. Appreciable amounts of ¹⁴C were incorporated into insoluble (polymeric) constituents even after relatively short periods of dark fixation.