Publications
| Title | Abstract | Year(sorted ascending) Filter | PMID Filter |
|---|
| [bacterial ecology of altered stones of monuments]. | 1964 | 14229540 | |
| path of sulfur in sulfide and thiosulfate oxidation by thiobacilli. | 1964 | 14231438 | |
| enzymic formation of haems and other metalloporphyrins. | 1964 | 14249145 | |
| [dna content and some problems of the evolution of photosynthetizing bacteria]. | 1964 | 14256083 | |
| the effects of thiosulphate and oxygen concentration on tetrathionate oxidation by thiobacillus x and t. thioparus. | 1964 | 5833373 | |
| sulfite oxidase of a facultative autotroph, thiobacillus novellus. | 1965 | 5840694 | |
| oxidation of elemental sulfur by an enzyme system of thiobacillus thiooxidans. | 1965 | 5855047 | |
| carbon dioxide fixation and carboxydismutase in thiobacillus novellus. | 1965 | 5860169 | |
| incorporation of atmospheric oxygen-18 into thiosulfate by the sulfur-oxidizing enzyme of thiobacillus thiooxidans. | 1965 | 5865170 | |
| [porphyrin pigments of green thiobacteria]. | 1965 | 5872731 | |
| [the system of thiobacteria]. | 1965 | 5881180 | |
| some properties of the rhodanese system of thiobacillus denitrificans. | 1. rhodanese has been extracted from thiobacillus denitrificans by ultrasonic disintegration of the cells. 2. studies with sephadex columns have shown that the enzyme aggregates, forming a tetramer. 3. the molecular weights of the monomer and of an enzymically active sub-unit one-quarter this size have been determined by gel filtration. 4. higher-molecular-weight forms of rhodanese are broken down by mercaptoethanol to enzymically active fragments of mol.wt. 7000 and 2000 respectively. 5. it is ... | 1965 | 5881654 |
| [adaptation of thiobacillus ferrooxidans to increased concentrations of hydrogen and iron ions]. | 1965 | 5887023 | |
| the taxonomy of certain thiobacilli. | 1965 | 5327415 | |
| oxidative phosphorylation in extracts of thiobacillus x. | 1965 | 4286344 | |
| effect of thiol-binding reagents on the metabolism of thiosulfate and tetrathionate by thiobacillus neapolitanus. | trudinger, p. a. (division of plant industry, canberra, australia). effect of thiol-binding reagents on the metabolism of thiosulfate and tetrathionate by thiobacillus neapolitanus. j. bacteriol. 89:617-625. 1965.-iodoacetamide, n-ethyl maleimide (nem), p-chloromercuribenzoate (cmb), mercurochrome, and hgcl(2) inhibited the oxidation of thiosulfate to sulfate by thiobacillus neapolitanus; tetrathionate accumulated under these conditions. high concentrations of the thiol-binding reagents lowered ... | 1965 | 14273636 |
| coupling of phosphorylation and carbon dioxide fixation in extracts of thiobacillus thioparus. | johnson, emmett j. (university of mississippi medical center, jackson), and harry d. peck, jr. coupling of phosphorylation and carbon dioxide fixation in extracts of thiobacillus thioparus. j. bacteriol. 89:1041-1050. 1965.-a cell-free system from thiobacillus thioparus which fixes large quantities of c(14)o(2) in the presence of ribose-5-phosphate, adenosine triphosphate (atp), and mg(++) has been described. the specific activity (0.041 mumole of ribulose-1,5-diphosphate min(-1) mg(-1) protein) ... | 1965 | 14276093 |
| studies on adenosine 5'-phosphosulfate reductase from desulfovibrio desulfuricans and thiobacillus thioparus. i. the assay and purification. | 1965 | 14314382 | |
| on the permeability of thiobacillus neapolitanus to thiosulphate. | 1965 | 14333083 | |
| thiosulfate oxidation and electron transport in thiobacillus novellus. | aleem, m. i. h. (research institute for advanced studies, baltimore, md.). thiosulfate oxidation and electron transport in thiobacillus novellus. j. bacteriol. 90:95-101. 1965.-a cell-free soluble enzyme system capable of oxidizing thiosulfate was obtained from thiobacillus novellus adapted to grow autotrophically. the enzyme systems of autotrophically grown cells brought about the transfer of electrons from thiosulfate to molecular oxygen via cytochromes of the c and a types; the reactions were ... | 1965 | 16562048 |
| phosphatidyl glycerol in thiobacillus thiooxidans. | 1965 | 14255675 | |
| fine structure of thiobacillus thiooxidans. | mahoney, robert p. (skidmore college, saratoga springs, n.y.), and mercedes r. edwards. fine structure of thiobacillus thiooxidans. j. bacteriol. 92: 487-495. 1966.-thin section analysis of the chemosynthetic autotroph thiobacillus thiooxidans revealed structures comparable to gram-negative heterotrophic bacteria. although this species is unique in that it oxidizes elemental sulfur for energy, uses carbon dioxide as its sole source of carbon, and can withstand a ph of less than 1, thin sections ... | 1966 | 16562139 |
| anaerobic production of thiobacillus denitrificans for the enzyme rhodanese. | a method for the anaerobic growth of thiobacillus denitrificans in a 140-liter (total capacity) stainless-steel culture vessel is described. as a result of controlling the ph value of cultures, and of ensuring that certain essential nutrients were in excess, cell yields approaching 700 mg (dry weight) per liter were obtained. these were over threefold higher than the best yields hitherto reported. the average rhodanese content of the cells from four cultures was 176,000 units per gram (dry weigh ... | 1966 | 16349709 |
| generation of reducing power in chemosynthesis. iv. energy-linked reduction of pyridine nucleotides by succinate in thiobacillus novellus. | 1966 | 4165956 | |
| iron oxidation by washed cell suspensions of the chemoautotroph, thiobacillus ferrooxidans. | 1966 | 5923135 | |
| media for sulphur bacteria. | 1966 | 5924318 | |
| membrane-associated sulfur oxidation by the autotroph thiobacillus thiooxidans. | adair, frank w. (rutgers, the state university, new brunswick, n. j.). membrane-associated sulfur oxidation by the autotroph thiobacillus thiooxidans. j. bacteriol. 92:899-904. 1966.-washed cell wall-membrane fragments derived from sulfur-grown cells of the strictly autotrophic bacterium, thiobacillus thiooxidans, oxidized elemental sulfur to sulfate without the addition of cofactors. the oxidation was optimal at ph 7.0 and was increased by the presence of wetting agents. oxygen uptake was inhib ... | 1966 | 5926757 |
| effects of organic matter on the growth of thiobacillus intermedius. | london, jack (university of california, los angeles), and sydney c. rittenberg. effects of organic matter on the growth of thiobacillus intermedius. j. bacteriol. 91:1062-1069. 1966.-yeast extract, glucose, glutamate, and other organic materials stimulate the rate and extent of growth of thiobacillus intermedius in thiosulfate broth. growth did not occur in glucose or glutamate mineral salts medium in the absence of thiosulfate, although a stable variant was obtained which grows on yeast extract ... | 1966 | 5929743 |
| absorption and utilization of organic matter by the strict autotroph, thiobacillus thiooxidans, with special reference to aspartic acid. | butler, richard g. (rutgers, the state university, new brunswick, n.j.), and wayne w. umbreit. absorption and utilization of organic matter by the strict autotroph, thiobacillus thiooxidans, with special reference to aspartic acid. j. bacteriol. 91:661-666. 1966.-the strictly autotrophic bacterium, thiobacillus thiooxidans, can be shown to assimilate a variety of organic materials. aspartic acid can be assimilated into protein and can be converted into co(2), but even in the presence of sulfur i ... | 1966 | 5934496 |
| the internal hydrogen ion concentration of thiobacillus thio-oxidans and survival after irradiation. | 1966 | 5941155 | |
| [35s]thiosulphate oxidation by thiobacillus strain c. | 1. thiobacillus strain c oxidized [(35)s]thiosulphate completely to sulphate. 2. during thiosulphate oxidation [(35)s]sulphate was formed more rapidly from (s.(35)so(3))(2-) than from ((35)s.so(3))(2-). (35)s disappeared less rapidly from thiosulphate with ((35)s.so(3))(2-) as substrate than with (s.(35)so(3))(2-). 3. thiosulphate labelled in both atoms was produced during ((35)s.so(3))(2-) oxidation, but not during (s.(35)so(3))(2-) oxidation. 4. no (35)s was precipitated as elementary sulphur ... | 1966 | 5941348 |
| energy coupling during sulphur compound oxidation by thiobacillus sp. strain c. | 1966 | 5954374 | |
| occurrence of the adenosine monophosphate inhibition of carbon dioxide fixation in photosynthetic and chemosynthetic autotrophs. | 1966 | 5954698 | |
| growth of some chemoautotrophic bacteria at different oxygen tensions. | 1966 | 5955989 | |
| acid production by thiobacillus thiooxidans. | 1966 | 5958116 | |
| growth of thiobacillus thiooxidans on glucose. | 1966 | 5961860 | |
| the initial product and properties of the sulfur-oxidizing enzyme of thiobacilli. | 1966 | 5968172 | |
| competitive inhibition of phosphoribulokinase by amp. | 1966 | 5970515 | |
| studies on adenosine-5'-phosphosulphate reductase from thiobacillus denitrificans. | 1966 | 5970862 | |
| taxonomy of the acidophilic thiobacilli. | 1966 | 5971385 | |
| formation of polythionates and their interrelationships during oxidation of thiosulfate by thiobacillus ferrooxidans. | 1966 | 5972638 | |
| oxidation of inorganic sulfur compounds by washed cell suspensions of thiobacillus ferrooxidans. | 1966 | 5972649 | |
| [occurrence of bacteria in underground waters in relation to the prevailing redox condition]. | 1966 | 6002795 | |
| [study on bacterial regeneration of ferric sulphate and on steeping of copper from ores]. | 1966 | 6002912 | |
| [the role of thionic bacteria in oxidation of sulphide ores of the kafanskoe bed]. | 1966 | 6003003 | |
| [microbiological investigation of some sulphide beds of north caucasus]. | 1966 | 4237160 | |
| anaerobic co2 fixation by autotrophic bacteria, hydrogenomonas and ferrobacillus. | 1966 | 4961096 | |
| generation of reducing power in chemosynthesis. 3. energy-linked reduction of pyridine nucleotides in thiobacillus novellus. | aleem, m. i. h. (research institute for advanced studies, baltimore, md.). generation of reducing power in chemosynthesis. iii. energy-linked reduction of pyridine nucleotides in thiobacillus novellus. j. bacteriol. 91:729-736. 1966.-cell-free extracts from thiobacillus novellus. catalyzed an adenosine triphosphate (atp)-dependent reduction of pyridine nucleotides anaerobically, or aerobically when the respiratory chain was inhibited by azide. the exogenous electron donor employed for the reduct ... | 1966 | 4379907 |
| amp-activation of an allosteric nad -dependent glutamate dehydrogenase. | 1967 | 4383078 | |
| on the uniqueness of the flagellum of thiobacillus thiooxidans. | 1967 | 5298435 | |
| influence of amino acids and organic antimetabolites on growth and biosynthesis of the chemoautotroph thiobacillus neapolitanus strain c. | 1967 | 5591183 | |
| the incorporation of acetate by the chemoautotroph thiobacillus neapolitanus strain c. | 1967 | 5600790 | |
| purification and some properties of sulfite oxidase from thiobacillus neapolitanus. | 1967 | 5602453 | |
| thiobacillus perometabolis nov. sp., a non-autotrophic thiobacillus. | 1967 | 5602460 | |
| biochemical basis of obligate autotrophy in blue-green algae and thiobacilli. | differential rates of incorporation of sugars, organic acids, and amino acids during autotrophic growth of several blue-green algae and thiobacilli have been determined. in obligate autotrophs (both blue-green algae and thiobacilli), exogenously furnished organic compounds make a very small contribution to cellular carbon; acetate, the most readily incorporated compound of those studied, contributes about 10% of newly synthesized cellular carbon. in thiobacillus intermedius, a facultative chemoa ... | 1967 | 4963789 |
| nonadaptive growth responses of tetrahymena pyriformis grown on single bacterial species. | 1967 | 4973773 | |
| keto acids as growth-limiting factors in autotrophic growth of thiobacillus thiooxidans. | when the strictly autotrophic bacterium thiobacillus thiooxidans was grown on sulfur, keto acids accumulated in the medium until they reached an inhibitory level at which growth ceased. much greater growth was possible if these substances were continually dialyzed out of the medium. | 1967 | 6020564 |
| yield coefficients of thiobacillus neapolitanus in continuous culture. | thiobacillus neapolitanus, when grown in continuous culture with thiosulfate limiting growth, possessed an apparent maximal molar growth yield of 8.0 g (dry weight) per mole of thiosulfate. the substrate requirement for energy of maintenance was the highest yet reported, amounting to 21.8 mmoles of thiosulfate per g per hr. the molar growth yield, corrected for this maintenance energy requirement, was 13.9 g (dry weight) per mole of thiosulfate. it was concluded that substrate-level phosphorylat ... | 1967 | 6025430 |
| taxonomy of anaerobic thiobacilli. | 1967 | 6034038 | |
| role of thiobacillus ferrooxidans in the oxidation of sulfide minerals. | 1967 | 6034412 | |
| phosphorylation coupled to the oxidation of sulfite and 2-mercaptoethanol in extracts of thiobacillus thioparus. | 1967 | 6036893 | |
| catabolite repression in the facultative chemoautotroph thiobacillus novellus. | several fermentable carbon sources were found to give rise to catabolite repression of all enzymes implicated in thiosulfate oxidation in the facultative chemoautotroph, thiobacillus novellus. glucose was found to elicit a strong repression. glycerol, lactate, lactose, ribose, and pyruvate caused marked repression. in all cases, the repression could be relieved only by returning the cells to a medium devoid of such fermentable substrates. on the other hand, carbon compounds (amino acids and orga ... | 1967 | 6057804 |
| [study of microbiological oxidative processes in the degtiar copper-pyrite deposits]. | 1967 | 6063203 | |
| marine thiobacilli. i. isolation and distribution. | 1967 | 6064043 | |
| marine thiobacilli. ii. culture and ultrastructure. | 1967 | 6064044 | |
| phospholipids of thiobacillus thiooxidans. | cells and spent growth media from sulfur- and thiosulfate-grown cultures of thiobacillus thiooxidans were analyzed. the phosphatides were examined by thinlayer chromatography, and the products of their hydrolysis by hydrochloric acid and methanolic potassium hydroxide were separated by paper chromatography. the phospholipids in both cells and spent growth media were identified as phosphatidyl ethanolamine, phosphatidyl-n-monomethylethanolamine, phosphatidyl glycerol, and diphosphatidyl glycerol. ... | 1967 | 6066049 |
| thiobacillus thiooxidans cell wall amino acids and monosaccharides. | 1967 | 6074409 | |
| studies on the sulfite-dependent atpase of a sulfur-oxidizing bacterium, thiobacillus thiooxidans. | 1967 | 4231493 | |
| effect of adenosine monophosphate, adenosine diphosphate, and reduced nicotinamide adenine dinucleotide on adenosine triphosphate-dependent carbon dioxide fixation in the autotroph thiobacillus neapolitanus. | the observation that adenosine triphosphate (atp)-dependent co(2) fixation in extracts of chemosynthetic and photosynthetic autotrophs may be regulated in part by adenosine monophosphate (amp) was extended to the strict autotroph thiobacillus neapolitanus (x). in addition, this report presents data which include adenosine diphosphate (adp) in the regulatory role. when the primary co(2) acceptor, ribose-5-phosphate, was replaced by ribulose-1,5-diphosphate, no inhibition of co(2) fixation occurre ... | 1967 | 4292312 |
| evidence for the calvin cycle and hexose monophosphate pathway in thiobacillus ferrooxidans. | the enzymes of the calvin reductive pentose phosphate cycle and the hexose monophosphate pathway have been demonstrated in cell-free extracts of thiobacillus ferrooxidans. this, together with analyses of the products of co(2) fixation in cell-free systems, suggests that these pathways are operative in whole cells of this microorganism. nevertheless, the amount of co(2) fixed in these cell-free systems was limited by the type and amount of compound added as substrate. the inability of cell extrac ... | 1967 | 4293079 |
| [electron transfer pathways in iron-oxidizing bacteria thiobacillus ferrooxidans]. | 1967 | 4385659 | |
| reduced nicotinamide adenine dinucleotide oxidation by thiobacillus neapolitanus and thiobacillus strain c. | 1968 | 4297023 | |
| staining technique for the genus thiobacillus. | 1968 | 4177308 | |
| sulfur-oxidizing enzyme of ferrobacillus ferrooxidans (thiobacillus ferrooxidans). | 1968 | 4968764 | |
| energy-coupling mechanisms in chemolithotrophic bacteria. | 1968 | 4972376 | |
| thiosulfate utilization by thiobacillus thiooxidans atcc 8085. | 1968 | 4867753 | |
| urea as a nitrogen source for thiobacilli. | 1968 | 4877133 | |
| inhibition of oxygen utilization and destruction of ubiquinone by ultraviolet irradiation of thiobacillus thiooxidans. | ultraviolet (uv) irradiation inhibited sulfur oxidation by cells of thiobacillus thiooxidans. sulfur-oxidizing activity decreased as the exposure time to uv light increased. a loss of the ability of cells of fix co(2) paralleled the loss of sulfur-oxidizing activity. uv light photoinactivated ubiquinone purified from t. thiooxidans. the same percentage of sulfur-oxidizing activity and ubiquinone was destroyed after 15 min of uv exposure. both the photoinactivation of sulfur oxidation and ubiquin ... | 1968 | 5636812 |
| allosteric regulation of phosphoribulokinase activity. | 1968 | 5642384 | |
| acetate assimilation by nitrobacter agilis in relation to its "obligate autotrophy". | acetate (1 to 10 mm) had no effect on the rate of nitrite oxidation or exponential growth by nitrobacter agilis. however, acetate-1-(14)c and -2-(14)c were both assimilated by growing cultures, and acetate carbon contributed 33 to 39% of newly synthesized cell carbon. carbon from acetate was incorporated into all of the major cell constituents, including most of the amino acids of cell protein and poly-beta-hydroxybutyrate (phb). cultures grown in the presence of acetate showed a significant inc ... | 1968 | 5643062 |
| phospholipids of the thiobacilli. | phosphatidyl glycerol, disphosphatidyl glycerol, and phosphatidyl ethanolamine were found in all of the thiobacillus species studied. t. thioparus possessed only these phospholipids. t. intermedius, t. neapolitanus, and t. thiooxidans contained phosphatidyl-n-monomethylethanolamine, and t. novellus lipids contained phosphatidyl-n-monomethylethanolamine, phosphatidyl-n-n-dimethylethanolamine, and phosphatidyl choline, in addition to the three phospholipids common to all of the thiobacilli. methio ... | 1968 | 5669895 |
| electron transport and coupled phosphorylation in the chemoautotroph thiobacillus neapolitanus. | 1968 | 5672145 | |
| deoxyribonucleic acid base composition and taxonomy of thiobacilli and some nitrifying bacteria. | 1968 | 5677980 | |
| direct sulfide oxidation in the solubilization of sulfide ores by thiobacillus ferrooxidans. | 1968 | 5686009 | |
| the thiosulfate-oxidizing enzyme of ferrobacillus ferrooxidans (thiobacillus ferrooxidans). | 1968 | 5687645 | |
| characterization of ribulose diphosphate carboxylase and phosphoribulokinase from thiobacillus thioparus and thiobacillus neapolitanus. | 1968 | 5697988 | |
| fluoroacetate toxicity in thiobacillus neapolitanus and its relevance to the problem of obligate chemoautotrophy. | 1968 | 5706422 | |
| [dependence of carbon dioxide fixation by thiobacilli on the acidity of the medium]. | 1968 | 5707058 | |
| oxidation of elemental sulfur by an enzyme system from thiobacillus neapolitanus. | 1968 | 5721907 | |
| [the effect of the acidity of the medium on the products of chemosynthesis of thiobacillus]. | 1968 | 5737736 | |
| fine structure of micrococcus denitrificans and m. halodenitrificans in relation to their taxonomy. | 1968 | 5300485 | |
| evidence for two species of glutamate dehydrogenases in thiobacillus novellus. | when grown autotrophically in a thiosulfate-mineral salts medium, cells of the facultative chemoautotrophic bacterium, thiobacillus novellus, produced two distinct glutamate dehydrogenases, one specific for nicotinamide adenine dinucleotide phosphate (nadp) and the other specific for nicotinamide adenine dinucleotide (nad). when glutamate was supplied exogenously as the sole carbon source, the nad-specific glutamate dehydrogenase was fully induced. lower levels of the enzyme were found in bacter ... | 1968 | 4384066 |
| [physiology of thiobactillus ferrooxidans]. | 1968 | 5271552 | |
| growth of thiobacillus ferrooxidans on various substrates. | 1969 | 5765173 | |
| chemoautotrophic sulfur bacteria in the marine environment. i. isolation, cultivation, and distribution. | 1969 | 5771611 | |
| chemoautotrophic sulfur bacteria from the marine environment. ii. characterization of an obligately marine facultative autotroph. | 1969 | 5771612 | |
| aromatic ring cleavage by a thiobacillus. | 1969 | 5773038 | |
| assimilation and metabolism of exogenous organic compounds by the strict autotrophs thiobacillus thioparus and thiobacillus neapolitanus. | the assimilation and utilization of the individual carbon atoms of pyruvate and acetate by cells of thiobacillus thioparus and t. neapolitanus, in the presence and absence of an energy source, were studied by use of radioactive substrates. both organisms produced (14)co(2) from (14)c-labeled pyruvate, but more came from carbon 1 than from carbons 2 or 3. the conversion of the carbons of acetate to co(2) by both organisms was much less than that from any of the pyruvate carbons. when labeled pyru ... | 1969 | 5776527 |
| the effect of some salts on thiobacillus thioparus. | 1969 | 5781759 | |
| isolation of an ornithine-containing lipid from thiobacillus thiooxidans. | the ornithine-containing lipid was separated from the other lipids of thiobacillus thiooxidans by thin-layer chromatography. the aminolipid possesses both amide and ester linkages. | 1969 | 5784231 |