Identification and characterization of alkaline phosphatase gene phoX in Microcystis aeruginosa PCC7806
PhoX is an extracellular alkaline phosphatase that is widely found in cyanobacteria and plays an important role in the conversion of extracellular organophosphorus into soluble inorganic phosphorus. However, the phoX gene has not yet been experimentally confirmed to exist in bloom-forming Microcysti...
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description | PhoX is an extracellular alkaline phosphatase that is widely found in cyanobacteria and plays an important role in the conversion of extracellular organophosphorus into soluble inorganic phosphorus. However, the
phoX
gene has not yet been experimentally confirmed to exist in bloom-forming
Microcystis
species. In this study, we identified a putative
phoX
gene (GenBank accession no. ARI79942.1) in
M. aeruginosa
PCC7806 and overexpressed it in
Escherichia coli
21 (DE3). The expressed PhoX protein displayed phosphodiesterase and phosphomonoesterase activities. In contrast to other bacterial PhoX proteins, which are activated mainly by Ca
2+
,
Microcysits
PhoX was most strongly activated by Mg
2+
, followed by Co
2+
, Ca
2+
, Zn
2+
and Mn
2+
, but it was inhibited by Ni
2+
. Sequence analysis showed that
phoX
was highly conserved in the
Microcystis
genus (DNA similarity > 96% between species).
phoX
expression responded significantly to different environmental phosphorus levels. When PCC7806 cells were cultured in phosphorus-deficient medium (BG11-P),
phoX
expression reached its highest level at 2 h and then decreased to a low level at 4 h. Organophosphate induced the expression of
phoX
; its expression reached the highest level at 4 h and was maintained at a high level at 6 h. Our results confirmed a putative
phoX
gene and demonstrated that the
phoX
gene of
Microcystis
is conserved. |
doi_str_mv | 10.1007/s13205-021-02774-z |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8052394</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2513579966</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-a20a3ac1a4816aa78eda8f7b88cc9f3bf7c55d9632cb3f4a9c966a36c36965393</originalsourceid><addsrcrecordid>eNp9kU1rFTEUhoNYbGn7B1xIwI2bqfmYfG0EudhaqOhCobtwbiYzN3Vuck1mhN5fb-zU68fCQEg45zlvzsmL0HNKLigh6nWhnBHREEbrVqpt9k_QCaOGNEJx_fRwZ7fH6LyUO1KXoMJQ8gwdc26kFpKfoOG683EKfXAwhRQxxA67DWRwk89hvwRTj2H8CmOIHu82qew2MEHxePBL4BaHiD8El5O7L1MoGHyehxBTAfxptVKayDN01MNY_PnjeYq-XL77vHrf3Hy8ul69vWlcq9qpAUaAg6PQaioBlPYd6F6ttXbO9HzdKydEZyRnbs37FowzUgKXjksjBTf8FL1ZdHfzeus7V4fLMNpdDlvI9zZBsH9nYtjYIX23mgjGTVsFXj0K5PRt9mWy21CcH0eIPs3FMsFaLY1SsqIv_0Hv0pxjHa9SlAtlanOVYgtVv6eU7PtDM5TYn1baxUpbrbQPVtp9LXrx5xiHkl_GVYAvQKmpOPj8--3_yP4AZ4-r1A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2513579966</pqid></control><display><type>article</type><title>Identification and characterization of alkaline phosphatase gene phoX in Microcystis aeruginosa PCC7806</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>SpringerLink Journals - AutoHoldings</source><creator>Hong, Sujuan ; Pan, Qianhui ; Chen, Siyu ; Zu, Yao ; Xu, Chongxin ; Li, Jianhong</creator><creatorcontrib>Hong, Sujuan ; Pan, Qianhui ; Chen, Siyu ; Zu, Yao ; Xu, Chongxin ; Li, Jianhong</creatorcontrib><description>PhoX is an extracellular alkaline phosphatase that is widely found in cyanobacteria and plays an important role in the conversion of extracellular organophosphorus into soluble inorganic phosphorus. However, the
phoX
gene has not yet been experimentally confirmed to exist in bloom-forming
Microcystis
species. In this study, we identified a putative
phoX
gene (GenBank accession no. ARI79942.1) in
M. aeruginosa
PCC7806 and overexpressed it in
Escherichia coli
21 (DE3). The expressed PhoX protein displayed phosphodiesterase and phosphomonoesterase activities. In contrast to other bacterial PhoX proteins, which are activated mainly by Ca
2+
,
Microcysits
PhoX was most strongly activated by Mg
2+
, followed by Co
2+
, Ca
2+
, Zn
2+
and Mn
2+
, but it was inhibited by Ni
2+
. Sequence analysis showed that
phoX
was highly conserved in the
Microcystis
genus (DNA similarity > 96% between species).
phoX
expression responded significantly to different environmental phosphorus levels. When PCC7806 cells were cultured in phosphorus-deficient medium (BG11-P),
phoX
expression reached its highest level at 2 h and then decreased to a low level at 4 h. Organophosphate induced the expression of
phoX
; its expression reached the highest level at 4 h and was maintained at a high level at 6 h. Our results confirmed a putative
phoX
gene and demonstrated that the
phoX
gene of
Microcystis
is conserved.</description><identifier>ISSN: 2190-572X</identifier><identifier>EISSN: 2190-5738</identifier><identifier>DOI: 10.1007/s13205-021-02774-z</identifier><identifier>PMID: 33968563</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Agriculture ; Alkaline phosphatase ; Bioinformatics ; Biomaterials ; Biotechnology ; Calcium ; Calcium ions ; Cancer Research ; Carbon dioxide ; Chemistry ; Chemistry and Materials Science ; Cobalt ; Conserved sequence ; Cyanobacteria ; Deoxyribonucleic acid ; DNA ; E coli ; Gene expression ; Low level ; Magnesium ; Manganese ; Microcystis ; Organophosphates ; Original ; Original Article ; Phosphatase ; Phosphodiesterase ; Phosphorus ; Proteins ; Sequence analysis ; Stem Cells ; Zinc</subject><ispartof>3 Biotech, 2021-05, Vol.11 (5), p.218-218, Article 218</ispartof><rights>King Abdulaziz City for Science and Technology 2021</rights><rights>King Abdulaziz City for Science and Technology 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-a20a3ac1a4816aa78eda8f7b88cc9f3bf7c55d9632cb3f4a9c966a36c36965393</citedby><cites>FETCH-LOGICAL-c474t-a20a3ac1a4816aa78eda8f7b88cc9f3bf7c55d9632cb3f4a9c966a36c36965393</cites><orcidid>0000-0002-4424-8986</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052394/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052394/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33968563$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hong, Sujuan</creatorcontrib><creatorcontrib>Pan, Qianhui</creatorcontrib><creatorcontrib>Chen, Siyu</creatorcontrib><creatorcontrib>Zu, Yao</creatorcontrib><creatorcontrib>Xu, Chongxin</creatorcontrib><creatorcontrib>Li, Jianhong</creatorcontrib><title>Identification and characterization of alkaline phosphatase gene phoX in Microcystis aeruginosa PCC7806</title><title>3 Biotech</title><addtitle>3 Biotech</addtitle><addtitle>3 Biotech</addtitle><description>PhoX is an extracellular alkaline phosphatase that is widely found in cyanobacteria and plays an important role in the conversion of extracellular organophosphorus into soluble inorganic phosphorus. However, the
phoX
gene has not yet been experimentally confirmed to exist in bloom-forming
Microcystis
species. In this study, we identified a putative
phoX
gene (GenBank accession no. ARI79942.1) in
M. aeruginosa
PCC7806 and overexpressed it in
Escherichia coli
21 (DE3). The expressed PhoX protein displayed phosphodiesterase and phosphomonoesterase activities. In contrast to other bacterial PhoX proteins, which are activated mainly by Ca
2+
,
Microcysits
PhoX was most strongly activated by Mg
2+
, followed by Co
2+
, Ca
2+
, Zn
2+
and Mn
2+
, but it was inhibited by Ni
2+
. Sequence analysis showed that
phoX
was highly conserved in the
Microcystis
genus (DNA similarity > 96% between species).
phoX
expression responded significantly to different environmental phosphorus levels. When PCC7806 cells were cultured in phosphorus-deficient medium (BG11-P),
phoX
expression reached its highest level at 2 h and then decreased to a low level at 4 h. Organophosphate induced the expression of
phoX
; its expression reached the highest level at 4 h and was maintained at a high level at 6 h. Our results confirmed a putative
phoX
gene and demonstrated that the
phoX
gene of
Microcystis
is conserved.</description><subject>Agriculture</subject><subject>Alkaline phosphatase</subject><subject>Bioinformatics</subject><subject>Biomaterials</subject><subject>Biotechnology</subject><subject>Calcium</subject><subject>Calcium ions</subject><subject>Cancer Research</subject><subject>Carbon dioxide</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Cobalt</subject><subject>Conserved sequence</subject><subject>Cyanobacteria</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>E coli</subject><subject>Gene expression</subject><subject>Low level</subject><subject>Magnesium</subject><subject>Manganese</subject><subject>Microcystis</subject><subject>Organophosphates</subject><subject>Original</subject><subject>Original Article</subject><subject>Phosphatase</subject><subject>Phosphodiesterase</subject><subject>Phosphorus</subject><subject>Proteins</subject><subject>Sequence analysis</subject><subject>Stem Cells</subject><subject>Zinc</subject><issn>2190-572X</issn><issn>2190-5738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU1rFTEUhoNYbGn7B1xIwI2bqfmYfG0EudhaqOhCobtwbiYzN3Vuck1mhN5fb-zU68fCQEg45zlvzsmL0HNKLigh6nWhnBHREEbrVqpt9k_QCaOGNEJx_fRwZ7fH6LyUO1KXoMJQ8gwdc26kFpKfoOG683EKfXAwhRQxxA67DWRwk89hvwRTj2H8CmOIHu82qew2MEHxePBL4BaHiD8El5O7L1MoGHyehxBTAfxptVKayDN01MNY_PnjeYq-XL77vHrf3Hy8ul69vWlcq9qpAUaAg6PQaioBlPYd6F6ttXbO9HzdKydEZyRnbs37FowzUgKXjksjBTf8FL1ZdHfzeus7V4fLMNpdDlvI9zZBsH9nYtjYIX23mgjGTVsFXj0K5PRt9mWy21CcH0eIPs3FMsFaLY1SsqIv_0Hv0pxjHa9SlAtlanOVYgtVv6eU7PtDM5TYn1baxUpbrbQPVtp9LXrx5xiHkl_GVYAvQKmpOPj8--3_yP4AZ4-r1A</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Hong, Sujuan</creator><creator>Pan, Qianhui</creator><creator>Chen, Siyu</creator><creator>Zu, Yao</creator><creator>Xu, Chongxin</creator><creator>Li, Jianhong</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4424-8986</orcidid></search><sort><creationdate>20210501</creationdate><title>Identification and characterization of alkaline phosphatase gene phoX in Microcystis aeruginosa PCC7806</title><author>Hong, Sujuan ; Pan, Qianhui ; Chen, Siyu ; Zu, Yao ; Xu, Chongxin ; Li, Jianhong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-a20a3ac1a4816aa78eda8f7b88cc9f3bf7c55d9632cb3f4a9c966a36c36965393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Agriculture</topic><topic>Alkaline phosphatase</topic><topic>Bioinformatics</topic><topic>Biomaterials</topic><topic>Biotechnology</topic><topic>Calcium</topic><topic>Calcium ions</topic><topic>Cancer Research</topic><topic>Carbon dioxide</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Cobalt</topic><topic>Conserved sequence</topic><topic>Cyanobacteria</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>E coli</topic><topic>Gene expression</topic><topic>Low level</topic><topic>Magnesium</topic><topic>Manganese</topic><topic>Microcystis</topic><topic>Organophosphates</topic><topic>Original</topic><topic>Original Article</topic><topic>Phosphatase</topic><topic>Phosphodiesterase</topic><topic>Phosphorus</topic><topic>Proteins</topic><topic>Sequence analysis</topic><topic>Stem Cells</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hong, Sujuan</creatorcontrib><creatorcontrib>Pan, Qianhui</creatorcontrib><creatorcontrib>Chen, Siyu</creatorcontrib><creatorcontrib>Zu, Yao</creatorcontrib><creatorcontrib>Xu, Chongxin</creatorcontrib><creatorcontrib>Li, Jianhong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>3 Biotech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hong, Sujuan</au><au>Pan, Qianhui</au><au>Chen, Siyu</au><au>Zu, Yao</au><au>Xu, Chongxin</au><au>Li, Jianhong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and characterization of alkaline phosphatase gene phoX in Microcystis aeruginosa PCC7806</atitle><jtitle>3 Biotech</jtitle><stitle>3 Biotech</stitle><addtitle>3 Biotech</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>11</volume><issue>5</issue><spage>218</spage><epage>218</epage><pages>218-218</pages><artnum>218</artnum><issn>2190-572X</issn><eissn>2190-5738</eissn><abstract>PhoX is an extracellular alkaline phosphatase that is widely found in cyanobacteria and plays an important role in the conversion of extracellular organophosphorus into soluble inorganic phosphorus. However, the
phoX
gene has not yet been experimentally confirmed to exist in bloom-forming
Microcystis
species. In this study, we identified a putative
phoX
gene (GenBank accession no. ARI79942.1) in
M. aeruginosa
PCC7806 and overexpressed it in
Escherichia coli
21 (DE3). The expressed PhoX protein displayed phosphodiesterase and phosphomonoesterase activities. In contrast to other bacterial PhoX proteins, which are activated mainly by Ca
2+
,
Microcysits
PhoX was most strongly activated by Mg
2+
, followed by Co
2+
, Ca
2+
, Zn
2+
and Mn
2+
, but it was inhibited by Ni
2+
. Sequence analysis showed that
phoX
was highly conserved in the
Microcystis
genus (DNA similarity > 96% between species).
phoX
expression responded significantly to different environmental phosphorus levels. When PCC7806 cells were cultured in phosphorus-deficient medium (BG11-P),
phoX
expression reached its highest level at 2 h and then decreased to a low level at 4 h. Organophosphate induced the expression of
phoX
; its expression reached the highest level at 4 h and was maintained at a high level at 6 h. Our results confirmed a putative
phoX
gene and demonstrated that the
phoX
gene of
Microcystis
is conserved.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>33968563</pmid><doi>10.1007/s13205-021-02774-z</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4424-8986</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Agriculture Alkaline phosphatase Bioinformatics Biomaterials Biotechnology Calcium Calcium ions Cancer Research Carbon dioxide Chemistry Chemistry and Materials Science Cobalt Conserved sequence Cyanobacteria Deoxyribonucleic acid DNA E coli Gene expression Low level Magnesium Manganese Microcystis Organophosphates Original Original Article Phosphatase Phosphodiesterase Phosphorus Proteins Sequence analysis Stem Cells Zinc |
title | Identification and characterization of alkaline phosphatase gene phoX in Microcystis aeruginosa PCC7806 |
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