Electrical properties of the plasma membrane of microplasmodia of Physarum polycephalum
Microplasmodia of Physarum polycephalum have been investigated by conventional electrophysiological techniques. In standard medium (30 mM K+, 4 mM Ca++, 3 mM Mg++, 18 mM citrate buffer, pH 4.7, 22 degrees C), the transmembrane potential difference Vm is around -100 mV and the membrane resistance abo...
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description | Microplasmodia of Physarum polycephalum have been investigated by conventional electrophysiological techniques. In standard medium (30 mM K+, 4 mM Ca++, 3 mM Mg++, 18 mM citrate buffer, pH 4.7, 22 degrees C), the transmembrane potential difference Vm is around -100 mV and the membrane resistance about 0.25 omega m2. Vm is insensitive to light and changes of the Na+/K+ ratio in the medium. Without bivalent cations in the medium and/or in presence of metabolic inhibitors (CCCP, CN-, N3-), Vm drops to about 0 mV. Under normal conditions, Vm is very sensitive to external pH (pH0), displaying an almost Nernstian slope at pH0 = 3. However, when measured during metabolic inhibition, Vm shows no sensitivity to pH0 over the range 3 to 6, only rising (about 50 mV/pH) at pH0 = 6. Addition of glucose or sucrose (but not mannitol or sorbitol) causes rapid depolarization, which partially recovers over the next few minutes. Half-maximal peak depolarization (25 mV with glucose) was achieved with 1 mM of the sugar. Sugar-induced depolarization was insensitive to pH0. The results are discussed on the basis of Class-I models of charge transport across biomembranes (Hansen, Gradmann, Sanders and Slayman, 1981, J. Membrane Biol. 63:165-190). Three transport systems are characterized: 1) An electrogenic H+ extrusion pump with a stoichiometry of 2 H+ per metabolic energy equivalent. The deprotonated form of the pump seems to be negatively charged. 2) In addition to the passive K+ pathways, there is a passive H+ transport system; here the protonated form seems to be positively charged. 3) A tentative H+-sugar cotransport system operates far from thermodynamic equilibrium, carrying negative charge in its deprotonated states. |
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In standard medium (30 mM K+, 4 mM Ca++, 3 mM Mg++, 18 mM citrate buffer, pH 4.7, 22 degrees C), the transmembrane potential difference Vm is around -100 mV and the membrane resistance about 0.25 omega m2. Vm is insensitive to light and changes of the Na+/K+ ratio in the medium. Without bivalent cations in the medium and/or in presence of metabolic inhibitors (CCCP, CN-, N3-), Vm drops to about 0 mV. Under normal conditions, Vm is very sensitive to external pH (pH0), displaying an almost Nernstian slope at pH0 = 3. However, when measured during metabolic inhibition, Vm shows no sensitivity to pH0 over the range 3 to 6, only rising (about 50 mV/pH) at pH0 = 6. Addition of glucose or sucrose (but not mannitol or sorbitol) causes rapid depolarization, which partially recovers over the next few minutes. Half-maximal peak depolarization (25 mV with glucose) was achieved with 1 mM of the sugar. Sugar-induced depolarization was insensitive to pH0. The results are discussed on the basis of Class-I models of charge transport across biomembranes (Hansen, Gradmann, Sanders and Slayman, 1981, J. Membrane Biol. 63:165-190). Three transport systems are characterized: 1) An electrogenic H+ extrusion pump with a stoichiometry of 2 H+ per metabolic energy equivalent. The deprotonated form of the pump seems to be negatively charged. 2) In addition to the passive K+ pathways, there is a passive H+ transport system; here the protonated form seems to be positively charged. 3) A tentative H+-sugar cotransport system operates far from thermodynamic equilibrium, carrying negative charge in its deprotonated states.</description><identifier>ISSN: 0022-2631</identifier><identifier>DOI: 10.1007/BF01872255</identifier><identifier>PMID: 7108943</identifier><language>eng</language><publisher>United States</publisher><subject>Azides - pharmacology ; Calcium - pharmacology ; Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology ; Cell Membrane - drug effects ; Cell Membrane - physiology ; Cyanides - pharmacology ; electrical properties ; Glucose - metabolism ; Kinetics ; membrane potential ; Membrane Potentials - drug effects ; Physarum - physiology ; Physarum polycephalum ; plasma membranes ; plasmodia ; Potassium - pharmacology ; Sodium - pharmacology ; Thermodynamics</subject><ispartof>The Journal of membrane biology, 1982-01, Vol.68 (1), p.67-77</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7108943$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fingerle, J</creatorcontrib><creatorcontrib>Gradmann, D</creatorcontrib><title>Electrical properties of the plasma membrane of microplasmodia of Physarum polycephalum</title><title>The Journal of membrane biology</title><addtitle>J Membr Biol</addtitle><description>Microplasmodia of Physarum polycephalum have been investigated by conventional electrophysiological techniques. In standard medium (30 mM K+, 4 mM Ca++, 3 mM Mg++, 18 mM citrate buffer, pH 4.7, 22 degrees C), the transmembrane potential difference Vm is around -100 mV and the membrane resistance about 0.25 omega m2. Vm is insensitive to light and changes of the Na+/K+ ratio in the medium. Without bivalent cations in the medium and/or in presence of metabolic inhibitors (CCCP, CN-, N3-), Vm drops to about 0 mV. Under normal conditions, Vm is very sensitive to external pH (pH0), displaying an almost Nernstian slope at pH0 = 3. However, when measured during metabolic inhibition, Vm shows no sensitivity to pH0 over the range 3 to 6, only rising (about 50 mV/pH) at pH0 = 6. Addition of glucose or sucrose (but not mannitol or sorbitol) causes rapid depolarization, which partially recovers over the next few minutes. Half-maximal peak depolarization (25 mV with glucose) was achieved with 1 mM of the sugar. Sugar-induced depolarization was insensitive to pH0. The results are discussed on the basis of Class-I models of charge transport across biomembranes (Hansen, Gradmann, Sanders and Slayman, 1981, J. Membrane Biol. 63:165-190). Three transport systems are characterized: 1) An electrogenic H+ extrusion pump with a stoichiometry of 2 H+ per metabolic energy equivalent. The deprotonated form of the pump seems to be negatively charged. 2) In addition to the passive K+ pathways, there is a passive H+ transport system; here the protonated form seems to be positively charged. 3) A tentative H+-sugar cotransport system operates far from thermodynamic equilibrium, carrying negative charge in its deprotonated states.</description><subject>Azides - pharmacology</subject><subject>Calcium - pharmacology</subject><subject>Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - physiology</subject><subject>Cyanides - pharmacology</subject><subject>electrical properties</subject><subject>Glucose - metabolism</subject><subject>Kinetics</subject><subject>membrane potential</subject><subject>Membrane Potentials - drug effects</subject><subject>Physarum - physiology</subject><subject>Physarum polycephalum</subject><subject>plasma membranes</subject><subject>plasmodia</subject><subject>Potassium - pharmacology</subject><subject>Sodium - pharmacology</subject><subject>Thermodynamics</subject><issn>0022-2631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAURT2ASiks7EiZ2AL-7LNHqCggVYIBxBjZ7osaZBNjJ0P_PanoznSlo6Orq0vIFaO3jFK4e1hTpoFzpU7InFLOa74U7Iycl_JFKQNYyhmZAaPaSDEnn48B_ZA7b0OVcp8wDx2Wqm-rYYdVCrZEW0WMLttvPODY-Uk78H7b2QN52-2LzWOsUh_2HtPOhjFekNPWhoKXx1yQj_Xj--q53rw-vazuN3XiAobaW6Eo3WrXGoPKAShQjsOEvGTAODojwHHtEJ33ptWCUcX8UlElW49SLMjNX-80_mfEMjSxKx5DmOb2Y2lAckXB8H9FpqQ2SptJvD6Ko4u4bVLuos375niZ-AWI4GuM</recordid><startdate>19820101</startdate><enddate>19820101</enddate><creator>Fingerle, J</creator><creator>Gradmann, D</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19820101</creationdate><title>Electrical properties of the plasma membrane of microplasmodia of Physarum polycephalum</title><author>Fingerle, J ; Gradmann, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p237t-ca3500d8bf99e5b77575b2700dc41712eb937b28beebcc9f831051c65054fce43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Azides - pharmacology</topic><topic>Calcium - pharmacology</topic><topic>Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology</topic><topic>Cell Membrane - drug effects</topic><topic>Cell Membrane - physiology</topic><topic>Cyanides - pharmacology</topic><topic>electrical properties</topic><topic>Glucose - metabolism</topic><topic>Kinetics</topic><topic>membrane potential</topic><topic>Membrane Potentials - drug effects</topic><topic>Physarum - physiology</topic><topic>Physarum polycephalum</topic><topic>plasma membranes</topic><topic>plasmodia</topic><topic>Potassium - pharmacology</topic><topic>Sodium - pharmacology</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fingerle, J</creatorcontrib><creatorcontrib>Gradmann, D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of membrane biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fingerle, J</au><au>Gradmann, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrical properties of the plasma membrane of microplasmodia of Physarum polycephalum</atitle><jtitle>The Journal of membrane biology</jtitle><addtitle>J Membr Biol</addtitle><date>1982-01-01</date><risdate>1982</risdate><volume>68</volume><issue>1</issue><spage>67</spage><epage>77</epage><pages>67-77</pages><issn>0022-2631</issn><abstract>Microplasmodia of Physarum polycephalum have been investigated by conventional electrophysiological techniques. In standard medium (30 mM K+, 4 mM Ca++, 3 mM Mg++, 18 mM citrate buffer, pH 4.7, 22 degrees C), the transmembrane potential difference Vm is around -100 mV and the membrane resistance about 0.25 omega m2. Vm is insensitive to light and changes of the Na+/K+ ratio in the medium. Without bivalent cations in the medium and/or in presence of metabolic inhibitors (CCCP, CN-, N3-), Vm drops to about 0 mV. Under normal conditions, Vm is very sensitive to external pH (pH0), displaying an almost Nernstian slope at pH0 = 3. However, when measured during metabolic inhibition, Vm shows no sensitivity to pH0 over the range 3 to 6, only rising (about 50 mV/pH) at pH0 = 6. Addition of glucose or sucrose (but not mannitol or sorbitol) causes rapid depolarization, which partially recovers over the next few minutes. Half-maximal peak depolarization (25 mV with glucose) was achieved with 1 mM of the sugar. Sugar-induced depolarization was insensitive to pH0. The results are discussed on the basis of Class-I models of charge transport across biomembranes (Hansen, Gradmann, Sanders and Slayman, 1981, J. Membrane Biol. 63:165-190). Three transport systems are characterized: 1) An electrogenic H+ extrusion pump with a stoichiometry of 2 H+ per metabolic energy equivalent. The deprotonated form of the pump seems to be negatively charged. 2) In addition to the passive K+ pathways, there is a passive H+ transport system; here the protonated form seems to be positively charged. 3) A tentative H+-sugar cotransport system operates far from thermodynamic equilibrium, carrying negative charge in its deprotonated states.</abstract><cop>United States</cop><pmid>7108943</pmid><doi>10.1007/BF01872255</doi><tpages>11</tpages></addata></record> |
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subjects | Azides - pharmacology Calcium - pharmacology Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology Cell Membrane - drug effects Cell Membrane - physiology Cyanides - pharmacology electrical properties Glucose - metabolism Kinetics membrane potential Membrane Potentials - drug effects Physarum - physiology Physarum polycephalum plasma membranes plasmodia Potassium - pharmacology Sodium - pharmacology Thermodynamics |
title | Electrical properties of the plasma membrane of microplasmodia of Physarum polycephalum |
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