Loading…
Immobilisation and biofilm development of Phanerochaete chrysosporium on polysulphone and ceramic membranes
In the design of a membrane bioreactor, the membrane morphology is a very important aspect, as the membrane should be developed or chosen to provide maximum surface area and an ideal environment for biofilm development. An investigation was carried out to identify membranes suitable for spore immobi...
Saved in:
Published in: | Journal of membrane science 2005-10, Vol.263 (1), p.30-37 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 37 |
container_issue | 1 |
container_start_page | 30 |
container_title | Journal of membrane science |
container_volume | 263 |
creator | Sheldon, M.S. Small, H.J. |
description | In the design of a membrane bioreactor, the membrane morphology is a very important aspect, as the membrane should be developed or chosen to provide maximum surface area and an ideal environment for biofilm development. An investigation was carried out to identify membranes suitable for spore immobilisation, biofilm development and extracellular enzyme production from
Phanerochaete chrysosporium. An internally skinned capillary polysulphone, two tubular aluminium oxide ceramic membranes with an average pore size of 0.2 and 3
μm respectively and one capillary titanium oxide ceramic membrane with an average pore size of 3
μm were identified and tested.
The highest attachment and immobilisation of spores were observed on the capillary membranes with less on the tubular ceramic membranes. On average biofilm thicknesses of 1140
μm were developed on the 3
μm capillary ceramic membrane, 830
μm on the capillary polysulphone membrane, 400
μm on the 3
μm tubular ceramic membrane with only 40
μm on the 0.2
μm tubular ceramic membrane. Continuous
LiP and
MnP enzyme production was achieved with both the polysulphone and capillary ceramic membrane reactors and no activity was detected with the tubular ceramic membrane reactors. However, for day-to-day operation of the reactor, the ceramic membranes were more rigid, mechanically stable and could be chemically and steam cleaned for re-use. |
doi_str_mv | 10.1016/j.memsci.2005.04.014 |
format | article |
fullrecord | <record><control><sourceid>proquest_elsev</sourceid><recordid>TN_cdi_proquest_miscellaneous_17069468</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0376738805002863</els_id><sourcerecordid>17069468</sourcerecordid><originalsourceid>FETCH-LOGICAL-e241t-ae954ecd64c3d438aa715e32a0b89e9a350f6e474506b023c0dddf64322a8653</originalsourceid><addsrcrecordid>eNotkMtOwzAQRS0EEuXxByyyYpcwjh0n2SChikelSrDo3nLsieISxyFOKvXvcSmr2dx7deYQ8kAho0DF0z5z6IK2WQ5QZMAzoPyCrGhVspTRnF2SFbBSpCWrqmtyE8IegJZQ1SvyvXHON7a3Qc3WD4kaTNJY39reJQYP2PvR4TAnvk2-OjXg5HWncMZEd9Mx-DD6yS4uic3R98ew9GPnB_yb0TgpZ3US2ZopVsMduWpVH_D-_96S3dvrbv2Rbj_fN-uXbYo5p3OqsC44aiO4ZoazSqmSFshyBU1VY61YAa1AXvICRAM502CMaQVnea4qUbBb8nieHSf_s2CYpbNBY99HBr8EGT8XNRdVDD6fgxhhDhYnGR3ioNHYCfUsjbeSgjwplnt5VixPiiVwGRWzX89udRc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17069468</pqid></control><display><type>article</type><title>Immobilisation and biofilm development of Phanerochaete chrysosporium on polysulphone and ceramic membranes</title><source>ScienceDirect Journals</source><creator>Sheldon, M.S. ; Small, H.J.</creator><creatorcontrib>Sheldon, M.S. ; Small, H.J.</creatorcontrib><description>In the design of a membrane bioreactor, the membrane morphology is a very important aspect, as the membrane should be developed or chosen to provide maximum surface area and an ideal environment for biofilm development. An investigation was carried out to identify membranes suitable for spore immobilisation, biofilm development and extracellular enzyme production from
Phanerochaete chrysosporium. An internally skinned capillary polysulphone, two tubular aluminium oxide ceramic membranes with an average pore size of 0.2 and 3
μm respectively and one capillary titanium oxide ceramic membrane with an average pore size of 3
μm were identified and tested.
The highest attachment and immobilisation of spores were observed on the capillary membranes with less on the tubular ceramic membranes. On average biofilm thicknesses of 1140
μm were developed on the 3
μm capillary ceramic membrane, 830
μm on the capillary polysulphone membrane, 400
μm on the 3
μm tubular ceramic membrane with only 40
μm on the 0.2
μm tubular ceramic membrane. Continuous
LiP and
MnP enzyme production was achieved with both the polysulphone and capillary ceramic membrane reactors and no activity was detected with the tubular ceramic membrane reactors. However, for day-to-day operation of the reactor, the ceramic membranes were more rigid, mechanically stable and could be chemically and steam cleaned for re-use.</description><identifier>ISSN: 0376-7388</identifier><identifier>EISSN: 1873-3123</identifier><identifier>DOI: 10.1016/j.memsci.2005.04.014</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Biofilm development ; Ceramic membranes ; Extracellular enzymes ; Lignin Peroxidase ; Manganese Peroxidase ; Membrane bioreactors ; Membranes ; Phanerochaete chrysosporium ; Polysulphone membranes ; Spore immobilisation</subject><ispartof>Journal of membrane science, 2005-10, Vol.263 (1), p.30-37</ispartof><rights>2005 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sheldon, M.S.</creatorcontrib><creatorcontrib>Small, H.J.</creatorcontrib><title>Immobilisation and biofilm development of Phanerochaete chrysosporium on polysulphone and ceramic membranes</title><title>Journal of membrane science</title><description>In the design of a membrane bioreactor, the membrane morphology is a very important aspect, as the membrane should be developed or chosen to provide maximum surface area and an ideal environment for biofilm development. An investigation was carried out to identify membranes suitable for spore immobilisation, biofilm development and extracellular enzyme production from
Phanerochaete chrysosporium. An internally skinned capillary polysulphone, two tubular aluminium oxide ceramic membranes with an average pore size of 0.2 and 3
μm respectively and one capillary titanium oxide ceramic membrane with an average pore size of 3
μm were identified and tested.
The highest attachment and immobilisation of spores were observed on the capillary membranes with less on the tubular ceramic membranes. On average biofilm thicknesses of 1140
μm were developed on the 3
μm capillary ceramic membrane, 830
μm on the capillary polysulphone membrane, 400
μm on the 3
μm tubular ceramic membrane with only 40
μm on the 0.2
μm tubular ceramic membrane. Continuous
LiP and
MnP enzyme production was achieved with both the polysulphone and capillary ceramic membrane reactors and no activity was detected with the tubular ceramic membrane reactors. However, for day-to-day operation of the reactor, the ceramic membranes were more rigid, mechanically stable and could be chemically and steam cleaned for re-use.</description><subject>Biofilm development</subject><subject>Ceramic membranes</subject><subject>Extracellular enzymes</subject><subject>Lignin Peroxidase</subject><subject>Manganese Peroxidase</subject><subject>Membrane bioreactors</subject><subject>Membranes</subject><subject>Phanerochaete chrysosporium</subject><subject>Polysulphone membranes</subject><subject>Spore immobilisation</subject><issn>0376-7388</issn><issn>1873-3123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNotkMtOwzAQRS0EEuXxByyyYpcwjh0n2SChikelSrDo3nLsieISxyFOKvXvcSmr2dx7deYQ8kAho0DF0z5z6IK2WQ5QZMAzoPyCrGhVspTRnF2SFbBSpCWrqmtyE8IegJZQ1SvyvXHON7a3Qc3WD4kaTNJY39reJQYP2PvR4TAnvk2-OjXg5HWncMZEd9Mx-DD6yS4uic3R98ew9GPnB_yb0TgpZ3US2ZopVsMduWpVH_D-_96S3dvrbv2Rbj_fN-uXbYo5p3OqsC44aiO4ZoazSqmSFshyBU1VY61YAa1AXvICRAM502CMaQVnea4qUbBb8nieHSf_s2CYpbNBY99HBr8EGT8XNRdVDD6fgxhhDhYnGR3ioNHYCfUsjbeSgjwplnt5VixPiiVwGRWzX89udRc</recordid><startdate>20051015</startdate><enddate>20051015</enddate><creator>Sheldon, M.S.</creator><creator>Small, H.J.</creator><general>Elsevier B.V</general><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20051015</creationdate><title>Immobilisation and biofilm development of Phanerochaete chrysosporium on polysulphone and ceramic membranes</title><author>Sheldon, M.S. ; Small, H.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e241t-ae954ecd64c3d438aa715e32a0b89e9a350f6e474506b023c0dddf64322a8653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biofilm development</topic><topic>Ceramic membranes</topic><topic>Extracellular enzymes</topic><topic>Lignin Peroxidase</topic><topic>Manganese Peroxidase</topic><topic>Membrane bioreactors</topic><topic>Membranes</topic><topic>Phanerochaete chrysosporium</topic><topic>Polysulphone membranes</topic><topic>Spore immobilisation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheldon, M.S.</creatorcontrib><creatorcontrib>Small, H.J.</creatorcontrib><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of membrane science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheldon, M.S.</au><au>Small, H.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immobilisation and biofilm development of Phanerochaete chrysosporium on polysulphone and ceramic membranes</atitle><jtitle>Journal of membrane science</jtitle><date>2005-10-15</date><risdate>2005</risdate><volume>263</volume><issue>1</issue><spage>30</spage><epage>37</epage><pages>30-37</pages><issn>0376-7388</issn><eissn>1873-3123</eissn><abstract>In the design of a membrane bioreactor, the membrane morphology is a very important aspect, as the membrane should be developed or chosen to provide maximum surface area and an ideal environment for biofilm development. An investigation was carried out to identify membranes suitable for spore immobilisation, biofilm development and extracellular enzyme production from
Phanerochaete chrysosporium. An internally skinned capillary polysulphone, two tubular aluminium oxide ceramic membranes with an average pore size of 0.2 and 3
μm respectively and one capillary titanium oxide ceramic membrane with an average pore size of 3
μm were identified and tested.
The highest attachment and immobilisation of spores were observed on the capillary membranes with less on the tubular ceramic membranes. On average biofilm thicknesses of 1140
μm were developed on the 3
μm capillary ceramic membrane, 830
μm on the capillary polysulphone membrane, 400
μm on the 3
μm tubular ceramic membrane with only 40
μm on the 0.2
μm tubular ceramic membrane. Continuous
LiP and
MnP enzyme production was achieved with both the polysulphone and capillary ceramic membrane reactors and no activity was detected with the tubular ceramic membrane reactors. However, for day-to-day operation of the reactor, the ceramic membranes were more rigid, mechanically stable and could be chemically and steam cleaned for re-use.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.memsci.2005.04.014</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0376-7388 |
ispartof | Journal of membrane science, 2005-10, Vol.263 (1), p.30-37 |
issn | 0376-7388 1873-3123 |
language | eng |
recordid | cdi_proquest_miscellaneous_17069468 |
source | ScienceDirect Journals |
subjects | Biofilm development Ceramic membranes Extracellular enzymes Lignin Peroxidase Manganese Peroxidase Membrane bioreactors Membranes Phanerochaete chrysosporium Polysulphone membranes Spore immobilisation |
title | Immobilisation and biofilm development of Phanerochaete chrysosporium on polysulphone and ceramic membranes |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T22%3A35%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_elsev&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immobilisation%20and%20biofilm%20development%20of%20Phanerochaete%20chrysosporium%20on%20polysulphone%20and%20ceramic%20membranes&rft.jtitle=Journal%20of%20membrane%20science&rft.au=Sheldon,%20M.S.&rft.date=2005-10-15&rft.volume=263&rft.issue=1&rft.spage=30&rft.epage=37&rft.pages=30-37&rft.issn=0376-7388&rft.eissn=1873-3123&rft_id=info:doi/10.1016/j.memsci.2005.04.014&rft_dat=%3Cproquest_elsev%3E17069468%3C/proquest_elsev%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-e241t-ae954ecd64c3d438aa715e32a0b89e9a350f6e474506b023c0dddf64322a8653%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=17069468&rft_id=info:pmid/&rfr_iscdi=true |