{"title":"Free and microencapsulated Erwinia herbicola for the production of tyrosine.","authors":"I Lloyd-George,&nbsp;T M Chang","doi":"10.3109/10731199309117370","DOIUrl":null,"url":null,"abstract":"<p><p>Erwinia herbicola (ATCC 21434) was grown in a medium which caused the cells to induce tyrosine phenol-lyase (TPL) activity. Whole cells of Erwinia herbicola were then microencapsulated within alginate-poly-L-lysine-alginate membraned microcapsules (diameter 800 microns). In a rotary shaker-incubator with a 1.9 cm horizontal throw, an agitation rate of at least 240 revolutions per minute (rpm) was required before the TPL activity of the microencapsulated cells was equal to that of the free cells. The TPL activity of the cells, whether free or microencapsulated, could be used for the conversion of ammonia, pyruvate and phenol into tyrosine at 37 degrees C. The results indicate that free cells and microencapsulated cells effect the conversion of these reactants to tyrosine equally well if the agitation rate is 240 rpm. In liver failure the concentrations of both ammonia, phenol and pyruvate are elevated. Hence the TPL activity of microencapsulated Erwinia herbicola could possibly find application in a novel approach for the removal of toxic phenol and ammonia during liver failure.</p>","PeriodicalId":77039,"journal":{"name":"Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology","volume":"21 3","pages":"323-33"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/10731199309117370","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3109/10731199309117370","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11

Abstract

Erwinia herbicola (ATCC 21434) was grown in a medium which caused the cells to induce tyrosine phenol-lyase (TPL) activity. Whole cells of Erwinia herbicola were then microencapsulated within alginate-poly-L-lysine-alginate membraned microcapsules (diameter 800 microns). In a rotary shaker-incubator with a 1.9 cm horizontal throw, an agitation rate of at least 240 revolutions per minute (rpm) was required before the TPL activity of the microencapsulated cells was equal to that of the free cells. The TPL activity of the cells, whether free or microencapsulated, could be used for the conversion of ammonia, pyruvate and phenol into tyrosine at 37 degrees C. The results indicate that free cells and microencapsulated cells effect the conversion of these reactants to tyrosine equally well if the agitation rate is 240 rpm. In liver failure the concentrations of both ammonia, phenol and pyruvate are elevated. Hence the TPL activity of microencapsulated Erwinia herbicola could possibly find application in a novel approach for the removal of toxic phenol and ammonia during liver failure.

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游离和微囊化Erwinia除草剂用于生产酪氨酸。
研究了除草剂欧文菌(Erwinia除草剂ATCC 21434)在诱导细胞酪氨酸酚裂解酶(TPL)活性的培养基中生长。用海藻酸盐-聚l -赖氨酸-海藻酸盐膜微胶囊(直径800微米)将整个细胞微胶囊化。在水平抛距1.9 cm的旋转摇床培养箱中,搅拌速度至少为240转/分钟(rpm),微胶囊细胞的TPL活性才与自由细胞相等。结果表明,当搅拌速率为240转/分时,游离细胞和微囊化细胞对氨、丙酮酸和苯酚转化为酪氨酸的效果相同。肝功能衰竭时氨、酚和丙酮酸的浓度升高。因此,微囊化Erwinia除草剂的TPL活性可能为肝衰竭过程中毒性苯酚和氨的去除提供新的途径。
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Polysaccharide microcapsules and macroporous beads for enhanced chromatographic separation. Polydisperse dextran as a diffusing test solute to study the membrane permeability of alginate polylysine microcapsules. Inhibition of endotoxin-mediated activation of endothelial cells by a perfluorocarbon emulsion. Proceedings of the 2nd Bioencapsulation Research Group Workshop. Cachan, France, April 6-8, 1992. The use of semifluorinated alkanes in blood-substitutes.
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