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Partition of lactic streptococcal bacteriophage during the ultrafiltration concentration of milk and whey
Milk and whey inoculated with lactic streptococcal bacteriophages 316, or 322, or both were concentrated by UF using a DDS Mini-Lab 20. The plate and frame unit was fitted with Type GR61PP polysulfone membrane with a 20,000 molecular weight cutoff. The unit was operated at an inlet pressure of .40 M...
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Published in: | Journal of dairy science 1987-10, Vol.70 (10), p.2013-2021 |
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container_end_page | 2021 |
container_issue | 10 |
container_start_page | 2013 |
container_title | Journal of dairy science |
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creator | Zottola, E.A Cogan, T.M Kelley, J |
description | Milk and whey inoculated with lactic streptococcal bacteriophages 316, or 322, or both were concentrated by UF using a DDS Mini-Lab 20. The plate and frame unit was fitted with Type GR61PP polysulfone membrane with a 20,000 molecular weight cutoff. The unit was operated at an inlet pressure of .40 MPa and an outlet pressure of .23 MPa with an initial flux of 2.0 to 3.0 L/h. Samples of retentate, permeate, and membrane were analyzed for the presence of bacteriophages. Under the conditions established in this study, phage particles did not pass through the membrane but instead became trapped in the polarization concentration layer or in the membrane. Phages were recovered from the membrane by extraction in sterile buffered water with the Stomacher. The UF concentration of milk containing the host species of Streptococcus cremoris resulted in phage propagation and lysis of the host but did not result in the passage of phages through the membrane. The UF processing of milk or whey should produce a phage-free permeate. |
doi_str_mv | 10.3168/jds.S0022-0302(87)80248-5 |
format | article |
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The plate and frame unit was fitted with Type GR61PP polysulfone membrane with a 20,000 molecular weight cutoff. The unit was operated at an inlet pressure of .40 MPa and an outlet pressure of .23 MPa with an initial flux of 2.0 to 3.0 L/h. Samples of retentate, permeate, and membrane were analyzed for the presence of bacteriophages. Under the conditions established in this study, phage particles did not pass through the membrane but instead became trapped in the polarization concentration layer or in the membrane. Phages were recovered from the membrane by extraction in sterile buffered water with the Stomacher. The UF concentration of milk containing the host species of Streptococcus cremoris resulted in phage propagation and lysis of the host but did not result in the passage of phages through the membrane. 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Ice creams ; PROCESAMIENTO ; PROCESSING ; STREPTOCOCCUS ; STREPTOCOCCUS CREMORIS ; SUERO DE LA LECHE ; TRAITEMENT ; ULTRAFILTRACION ; ULTRAFILTRATION ; WHEY</subject><ispartof>Journal of dairy science, 1987-10, Vol.70 (10), p.2013-2021</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-caa61f44b395f1f401809b348266b002c154818e178487fc88ac1ff8146eba7f3</citedby><cites>FETCH-LOGICAL-c473t-caa61f44b395f1f401809b348266b002c154818e178487fc88ac1ff8146eba7f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8389208$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3680722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zottola, E.A</creatorcontrib><creatorcontrib>Cogan, T.M</creatorcontrib><creatorcontrib>Kelley, J</creatorcontrib><title>Partition of lactic streptococcal bacteriophage during the ultrafiltration concentration of milk and whey</title><title>Journal of dairy science</title><addtitle>J Dairy Sci</addtitle><description>Milk and whey inoculated with lactic streptococcal bacteriophages 316, or 322, or both were concentrated by UF using a DDS Mini-Lab 20. The plate and frame unit was fitted with Type GR61PP polysulfone membrane with a 20,000 molecular weight cutoff. The unit was operated at an inlet pressure of .40 MPa and an outlet pressure of .23 MPa with an initial flux of 2.0 to 3.0 L/h. Samples of retentate, permeate, and membrane were analyzed for the presence of bacteriophages. Under the conditions established in this study, phage particles did not pass through the membrane but instead became trapped in the polarization concentration layer or in the membrane. Phages were recovered from the membrane by extraction in sterile buffered water with the Stomacher. The UF concentration of milk containing the host species of Streptococcus cremoris resulted in phage propagation and lysis of the host but did not result in the passage of phages through the membrane. The UF processing of milk or whey should produce a phage-free permeate.</description><subject>Animals</subject><subject>BACTERIOFAGOS</subject><subject>BACTERIOPHAGE</subject><subject>BACTERIOPHAGES</subject><subject>Biological and medical sciences</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>LACTOSERUM</subject><subject>LAIT</subject><subject>LECHE</subject><subject>MILK</subject><subject>Milk - microbiology</subject><subject>Milk and cheese industries. 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Psychology</topic><topic>LACTOSERUM</topic><topic>LAIT</topic><topic>LECHE</topic><topic>MILK</topic><topic>Milk - microbiology</topic><topic>Milk and cheese industries. Ice creams</topic><topic>PROCESAMIENTO</topic><topic>PROCESSING</topic><topic>STREPTOCOCCUS</topic><topic>STREPTOCOCCUS CREMORIS</topic><topic>SUERO DE LA LECHE</topic><topic>TRAITEMENT</topic><topic>ULTRAFILTRACION</topic><topic>ULTRAFILTRATION</topic><topic>WHEY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zottola, E.A</creatorcontrib><creatorcontrib>Cogan, T.M</creatorcontrib><creatorcontrib>Kelley, J</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 50</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dairy science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zottola, E.A</au><au>Cogan, T.M</au><au>Kelley, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Partition of lactic streptococcal bacteriophage during the ultrafiltration concentration of milk and whey</atitle><jtitle>Journal of dairy science</jtitle><addtitle>J Dairy Sci</addtitle><date>1987-10-01</date><risdate>1987</risdate><volume>70</volume><issue>10</issue><spage>2013</spage><epage>2021</epage><pages>2013-2021</pages><issn>0022-0302</issn><eissn>1525-3198</eissn><coden>JDSCAE</coden><abstract>Milk and whey inoculated with lactic streptococcal bacteriophages 316, or 322, or both were concentrated by UF using a DDS Mini-Lab 20. The plate and frame unit was fitted with Type GR61PP polysulfone membrane with a 20,000 molecular weight cutoff. The unit was operated at an inlet pressure of .40 MPa and an outlet pressure of .23 MPa with an initial flux of 2.0 to 3.0 L/h. Samples of retentate, permeate, and membrane were analyzed for the presence of bacteriophages. Under the conditions established in this study, phage particles did not pass through the membrane but instead became trapped in the polarization concentration layer or in the membrane. Phages were recovered from the membrane by extraction in sterile buffered water with the Stomacher. The UF concentration of milk containing the host species of Streptococcus cremoris resulted in phage propagation and lysis of the host but did not result in the passage of phages through the membrane. The UF processing of milk or whey should produce a phage-free permeate.</abstract><cop>Savoy, IL</cop><pub>Am Dairy Sci Assoc</pub><pmid>3680722</pmid><doi>10.3168/jds.S0022-0302(87)80248-5</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals BACTERIOFAGOS BACTERIOPHAGE BACTERIOPHAGES Biological and medical sciences Food industries Fundamental and applied biological sciences. Psychology LACTOSERUM LAIT LECHE MILK Milk - microbiology Milk and cheese industries. Ice creams PROCESAMIENTO PROCESSING STREPTOCOCCUS STREPTOCOCCUS CREMORIS SUERO DE LA LECHE TRAITEMENT ULTRAFILTRACION ULTRAFILTRATION WHEY |
title | Partition of lactic streptococcal bacteriophage during the ultrafiltration concentration of milk and whey |
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