File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Degradation of purified terephthalic acid and expression of mnp gene for GEM Fhhh

TitleDegradation of purified terephthalic acid and expression of mnp gene for GEM Fhhh
遺傳工程菌Fhhh降解精對苯二甲酸與mnp基因表達
Authors
KeywordsInter-kingdom protoplast fusant
Phanerochaete chrysosporium
Purified terephthalic acid
The specific degradation rate
Manganese peroxidase
Issue Date2002
Publisher科學出版社. The Journal's web site is located at http://c.g.wanfangdata.com.cn/Periodical-hjkxxb.aspx
Citation
環境科學學報, 2002, v. 22 n. 1, p. 1-5 How to Cite?
Acta Scientiae Circumstantiae, 2002, v. 22 n. 1, p. 1-5 How to Cite?
AbstractThe levels of the specific degradation rate (SDR) for the genetically engineered microorganism (GEM) Fhhh from inter-kingdom protoplast fusion and the parental strain \%Phanerochaete chrysosporium\% (PC) in degradation of purified terephthalic acid (PTA) were affected by (NH-4)-2C-4H-4O-6,H-2O-2,Mn+{2+},and pH value.Except pH value,the other 3 factors affecting the SDR levels had a same order for both strains.The pH value in the order was at the first site for Fhhh,and that for PC at the third site.At the optimal levels,the SDR value of Fhhh was 11^11% higher than that of PC;the value of manganese peroxidase specific activity (MnP|SA) of Fhhh was 15^22% higher than that of PC.There was a positive relationship between SDR and MnP|SA significantly.The optimal levels of 4 factors for SDR also were the optimal levels for mnp gene expression.The technique of the mnp gene expression control would be useful to treat PTA wastewater.
Persistent Identifierhttp://hdl.handle.net/10722/73181
ISSN
2015 SCImago Journal Rankings: 0.154

 

DC FieldValueLanguage
dc.contributor.authorCheng, Sen_HK
dc.contributor.authorChen, Len_HK
dc.contributor.authorYan, Jen_HK
dc.contributor.authorHao, Cen_HK
dc.contributor.authorLi, Wen_HK
dc.contributor.authorGu, Jen_HK
dc.contributor.authorCheng, Gen_HK
dc.contributor.authorChen, Nen_HK
dc.date.accessioned2010-09-06T06:48:55Z-
dc.date.available2010-09-06T06:48:55Z-
dc.date.issued2002en_HK
dc.identifier.citation環境科學學報, 2002, v. 22 n. 1, p. 1-5en_HK
dc.identifier.citationActa Scientiae Circumstantiae, 2002, v. 22 n. 1, p. 1-5-
dc.identifier.issn0253-2468-
dc.identifier.urihttp://hdl.handle.net/10722/73181-
dc.description.abstractThe levels of the specific degradation rate (SDR) for the genetically engineered microorganism (GEM) Fhhh from inter-kingdom protoplast fusion and the parental strain \%Phanerochaete chrysosporium\% (PC) in degradation of purified terephthalic acid (PTA) were affected by (NH-4)-2C-4H-4O-6,H-2O-2,Mn+{2+},and pH value.Except pH value,the other 3 factors affecting the SDR levels had a same order for both strains.The pH value in the order was at the first site for Fhhh,and that for PC at the third site.At the optimal levels,the SDR value of Fhhh was 11^11% higher than that of PC;the value of manganese peroxidase specific activity (MnP|SA) of Fhhh was 15^22% higher than that of PC.There was a positive relationship between SDR and MnP|SA significantly.The optimal levels of 4 factors for SDR also were the optimal levels for mnp gene expression.The technique of the mnp gene expression control would be useful to treat PTA wastewater.-
dc.languagechien_HK
dc.publisher科學出版社. The Journal's web site is located at http://c.g.wanfangdata.com.cn/Periodical-hjkxxb.aspx-
dc.relation.ispartof環境科學學報en_HK
dc.relation.ispartofActa Scientiae Circumstantiae-
dc.subjectInter-kingdom protoplast fusant-
dc.subjectPhanerochaete chrysosporium-
dc.subjectPurified terephthalic acid-
dc.subjectThe specific degradation rate-
dc.subjectManganese peroxidase-
dc.titleDegradation of purified terephthalic acid and expression of mnp gene for GEM Fhhhen_HK
dc.title遺傳工程菌Fhhh降解精對苯二甲酸與mnp基因表達-
dc.typeArticleen_HK
dc.identifier.emailGu, J: jdgu@hkucc.hku.hken_HK
dc.identifier.authorityGu, J=rp00701en_HK
dc.identifier.doi10.3321/j.issn:0253-2468.2002.01.001-
dc.identifier.hkuros69667en_HK
dc.identifier.volume22-
dc.identifier.issue1-
dc.identifier.spage1-
dc.identifier.epage5-
dc.publisher.placeChina-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats