An FeIII dinuclear metallacycle complex as a size-selective adsorbent for nitrogenous compounds and a potentially effective ammonia storage material

In this research, PHA (polyhydroxyalkanoate) production system by activated sludge was studied. PHA behaves as carbon and energy storage material in bacteria. And PHA is a biodegradable plastic when extracted from bacteria. In this paper, the investigations from 3 aspects were reported; control of PHA composition, PHA production under coexistence of nitrogenous compounds, and influence of enrichment condition on PHA productivity. As results, it was possible to regulate PHA composition by utilizing acetate and propionate as carbon source and by regulating its composition. Nitrogenous compounds did not depress PHA productivities in the case of activated sludge, while nitrogenous compounds usually depress in general. PHA contents of MLSS were achieved up to 57% by using anaerobic-aerobic activated sludge. But microaerophilic-aerobic process could supply stably the activated sludge which accumulated PHA with high efficiency.

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Ammonia Adsorption on Ion Exchanged Y-zeolites as Ammonia Storage Material

Journal of the Japan Petroleum Institute ◽

10.1627/jpi.46.301 ◽

2003 ◽

Vol 46 (5) ◽

pp. 301-307 ◽

Cited By ~ 25

Author(s):

Chun Yi LIU ◽

Ken-ichi AIKA

Keyword(s):

Storage Material ◽

Ammonia Adsorption ◽

Y Zeolites ◽

Ammonia Storage

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Effect of the Cl/Br Molar Ratio of a CaCl2−CaBr2Mixture Used as an Ammonia Storage Material

Industrial & Engineering Chemistry Research ◽

10.1021/ie049873i ◽

2004 ◽

Vol 43 (22) ◽

pp. 6994-7000 ◽

Cited By ~ 14

Author(s):

Chun Yi Liu ◽

Ken-ichi Aika

Keyword(s):

Molar Ratio ◽

Storage Material ◽

Ammonia Storage

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The diagnosis of metabolic storage disease in skin biopsies (a light-, electronmicroscopic, and analytical study)

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100084119 ◽

1978 ◽

Vol 36 (2) ◽

pp. 648-649

Author(s):

W. Jurecka ◽

W. Gebhart ◽

H. Lassmann

Keyword(s):

Storage Disease ◽

Hunter Syndrome ◽

Histochemical Demonstration ◽

Sweat Glands ◽

Type I ◽

Storage Material ◽

Scheie Syndrome ◽

Storage Products ◽

Skin Biopsies ◽

Type V

Diagnosis of metabolic storage disease can be established by the determination of enzymes or storage material in blood, urine, or several tissues or by clinical parameters. Identification of the accumulated storage products is possible by biochemical analysis of isolated material, by histochemical demonstration in sections, or by ultrastructural demonstration of typical inclusion bodies. In order to determine the significance of such inclusions in human skin biopsies several types of metabolic storage disease were investigated. The following results were obtained.In MPS type I (Pfaundler-Hurler-Syndrome), type II (Hunter-Syndrome), and type V (Ullrich-Scheie-Syndrome) mainly “empty” vacuoles were found in skin fibroblasts, in Schwann cells, keratinocytes and macrophages (Dorfmann and Matalon 1972). In addition, prominent vacuolisation was found in eccrine sweat glands. The storage material could be preserved in part by fixation with cetylpyridiniumchloride and was also present within fibroblasts grown in tissue culture.

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Electron Microscopy in the diagnosis of lysosomal storage diseases

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100156316 ◽

1989 ◽

Vol 47 ◽

pp. 866-867

Author(s):

Carole Vogler ◽

Harvey S. Rosenberg

Keyword(s):

Electron Microscopy ◽

Lysosomal Enzyme ◽

Rectal Mucosa ◽

Lysosomal Storage Diseases ◽

Cell Types ◽

Lysosomal Storage ◽

Storage Material ◽

Ultrastructural Examination ◽

Blood Leukocytes ◽

Storage Diseases

Diagnostic procedures for evaluation of patients with lysosomal storage diseases (LSD) seek to identify a deficiency of a responsible lysosomal enzyme or accumulation of a substance that requires the missing enzyme for degradation. Most patients with LSD have progressive neurological degeneration and may have a variety of musculoskeletal and visceral abnormalities. In the LSD, the abnormally diminished lysosomal enzyme results in accumulation of unmetabolized catabolites in distended lysosomes. Because of the subcellular morphology and size of lysosomes, electron microscopy is an ideal tool to study tissue from patients with suspected LSD. In patients with LSD all cells lack the specific lysosomal enzyme but the distribution of storage material is dependent on the extent of catabolism of the substrate in each cell type under normal circumstances. Lysosmal storages diseases affect many cell types and tissues. Storage material though does not accumulate in all tissues and cell types and may be different biochemically and morphologically in different tissues.Conjunctiva, skin, rectal mucosa and peripheral blood leukocytes may show ultrastructural evidence of lysosomal storage even in the absence of clinical findings and thus any of these tissues can be used for ultrastructural examination in the diagnostic evaluation of patients with suspected LSD. Biopsy of skin and conjunctiva are easily obtained and provide multiple cell types including endothelium, epithelium, fibroblasts and nerves for ultrastructural study. Fibroblasts from skin and conjunctiva can also be utilized for the initiation of tissue cultures for chemical assays. Brain biopsy has been largely replaced by biopsy of more readily obtained tissue and by biochemical assays. Such assays though may give equivical or nondiagnostic results and in some lysosomal storage diseases an enzyme defect has not yet been identified and diagnoses can be made only by ultrastructural examination.

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