The kinetics of embryo drying in Drosophila melanogaster as a function of the steps in permeabilization: Experimental
The Drosophila embryo is surrounded by an outer chorion and an inner vitelline membrane that are an effective barrier to the movement of water. The chorion can be removed by 2.5% hypochlorite (1). If surface water is then removed by isopropanol (2), the vitelline membrane can be rendered permeable t...
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Veröffentlicht in: | Journal of insect physiology 1996, Vol.42 (5), p.501-516 |
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description | The
Drosophila embryo is surrounded by an outer chorion and an inner vitelline membrane that are an effective barrier to the movement of water. The chorion can be removed by 2.5% hypochlorite (1). If surface water is then removed by isopropanol (2), the vitelline membrane can be rendered permeable to water by heptane containing 0.3% 1-butanol (3). Here, we determined quantitatively the effects of these three steps on the permeability of the embryo to water. Permeability was assessed by exposing embryos to air at 22–23 °C and approx. 56% r.h. and determining weight loss with time. We also determined the effect of the three permeabilization steps on the water and solids contents of the embryos initially, after equilibration with air, and after complete drying. The intact embryo contains 76% (
w
w
) water and 24% solids. The successive permeabilization steps produce small increases in the former and small decreases in the latter. Intact embryos require 5–12h to lose half their water, the longer times being applicable to older embryos. After permeabilization steps (1), (1) + (2), and (1) + (2) + (3) the times for 50% water loss decrease to 1.6, 1.9, and 0.1 h, respectively. |
doi_str_mv | 10.1016/0022-1910(95)00122-0 |
format | Article |
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Drosophila embryo is surrounded by an outer chorion and an inner vitelline membrane that are an effective barrier to the movement of water. The chorion can be removed by 2.5% hypochlorite (1). If surface water is then removed by isopropanol (2), the vitelline membrane can be rendered permeable to water by heptane containing 0.3% 1-butanol (3). Here, we determined quantitatively the effects of these three steps on the permeability of the embryo to water. Permeability was assessed by exposing embryos to air at 22–23 °C and approx. 56% r.h. and determining weight loss with time. We also determined the effect of the three permeabilization steps on the water and solids contents of the embryos initially, after equilibration with air, and after complete drying. The intact embryo contains 76% (
w
w
) water and 24% solids. The successive permeabilization steps produce small increases in the former and small decreases in the latter. Intact embryos require 5–12h to lose half their water, the longer times being applicable to older embryos. After permeabilization steps (1), (1) + (2), and (1) + (2) + (3) the times for 50% water loss decrease to 1.6, 1.9, and 0.1 h, respectively.</description><identifier>ISSN: 0022-1910</identifier><identifier>EISSN: 1879-1611</identifier><identifier>DOI: 10.1016/0022-1910(95)00122-0</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>air drying ; body water ; butanol ; chemical treatment ; dechorionation ; Diptera ; Drosophila melanogaster ; Drosophilidae ; embryo (animal) ; Embryo dehydration ; embryo permeabilization ; embryo solids ; embryo water loss ; heptane ; isopropyl alcohol ; kinetics ; Membrane permeability ; membranes ; Permeabilization protocol ; removal ; vitelline membrane ; Water and solids content ; water content</subject><ispartof>Journal of insect physiology, 1996, Vol.42 (5), p.501-516</ispartof><rights>1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c359t-1d5a14ed9b0cda716271398430c049ad922c66e9127df3f362694f8a65edcc643</citedby><cites>FETCH-LOGICAL-c359t-1d5a14ed9b0cda716271398430c049ad922c66e9127df3f362694f8a65edcc643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0022-1910(95)00122-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Schreuders, P.D.</creatorcontrib><creatorcontrib>Kassis, J.N.</creatorcontrib><creatorcontrib>Cole, K.W.</creatorcontrib><creatorcontrib>Schneider, U.</creatorcontrib><creatorcontrib>Mahowald, A.P.</creatorcontrib><creatorcontrib>Mazur, P.</creatorcontrib><title>The kinetics of embryo drying in Drosophila melanogaster as a function of the steps in permeabilization: Experimental</title><title>Journal of insect physiology</title><description>The
Drosophila embryo is surrounded by an outer chorion and an inner vitelline membrane that are an effective barrier to the movement of water. The chorion can be removed by 2.5% hypochlorite (1). If surface water is then removed by isopropanol (2), the vitelline membrane can be rendered permeable to water by heptane containing 0.3% 1-butanol (3). Here, we determined quantitatively the effects of these three steps on the permeability of the embryo to water. Permeability was assessed by exposing embryos to air at 22–23 °C and approx. 56% r.h. and determining weight loss with time. We also determined the effect of the three permeabilization steps on the water and solids contents of the embryos initially, after equilibration with air, and after complete drying. The intact embryo contains 76% (
w
w
) water and 24% solids. The successive permeabilization steps produce small increases in the former and small decreases in the latter. Intact embryos require 5–12h to lose half their water, the longer times being applicable to older embryos. After permeabilization steps (1), (1) + (2), and (1) + (2) + (3) the times for 50% water loss decrease to 1.6, 1.9, and 0.1 h, respectively.</description><subject>air drying</subject><subject>body water</subject><subject>butanol</subject><subject>chemical treatment</subject><subject>dechorionation</subject><subject>Diptera</subject><subject>Drosophila melanogaster</subject><subject>Drosophilidae</subject><subject>embryo (animal)</subject><subject>Embryo dehydration</subject><subject>embryo permeabilization</subject><subject>embryo solids</subject><subject>embryo water loss</subject><subject>heptane</subject><subject>isopropyl alcohol</subject><subject>kinetics</subject><subject>Membrane permeability</subject><subject>membranes</subject><subject>Permeabilization protocol</subject><subject>removal</subject><subject>vitelline membrane</subject><subject>Water and solids content</subject><subject>water content</subject><issn>0022-1910</issn><issn>1879-1611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNp9kMGOFCEURYnRxHb0D0xkZXRR-h4UVOPCZDLOqMkkLpxZExpe9aBVRQnVxvbrh7KNS1cEOPfBPYw9R3iDgPotgBANGoRXRr0GwLqDB2yD2840qBEfss0_5DF7Uso3AFB6qzbscHNH_HucaIm-8NRzGnf5mHjIxzjteZz4h5xKmu_i4PhIg5vS3pWFMneFO94fJr_ENK3JpU6qN3NZUzPlkdwuDvG3W4F3_PJXPYsjTYsbnrJHvRsKPfu7nrHbq8ubi0_N9ZePny_OrxsvlVkaDMphS8HswAfXoRYdSrNtJXhojQtGCK81GRRd6GUvtdCm7bdOKwre61aesZenuXNOPw5UFjvG4mmoNSgdikWllawuKtieQF_blky9netfXT5aBLs6tqtAuwq0Rtk_ju0ae3GK9S5Zt8-x2NuvAlACKoGdlpV4fyKo1vwZKdviI02eQszkFxtS_P8T9_1DjUM</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>Schreuders, P.D.</creator><creator>Kassis, J.N.</creator><creator>Cole, K.W.</creator><creator>Schneider, U.</creator><creator>Mahowald, A.P.</creator><creator>Mazur, P.</creator><general>Elsevier Ltd</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SS</scope></search><sort><creationdate>1996</creationdate><title>The kinetics of embryo drying in Drosophila melanogaster as a function of the steps in permeabilization: Experimental</title><author>Schreuders, P.D. ; Kassis, J.N. ; Cole, K.W. ; Schneider, U. ; Mahowald, A.P. ; Mazur, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-1d5a14ed9b0cda716271398430c049ad922c66e9127df3f362694f8a65edcc643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>air drying</topic><topic>body water</topic><topic>butanol</topic><topic>chemical treatment</topic><topic>dechorionation</topic><topic>Diptera</topic><topic>Drosophila melanogaster</topic><topic>Drosophilidae</topic><topic>embryo (animal)</topic><topic>Embryo dehydration</topic><topic>embryo permeabilization</topic><topic>embryo solids</topic><topic>embryo water loss</topic><topic>heptane</topic><topic>isopropyl alcohol</topic><topic>kinetics</topic><topic>Membrane permeability</topic><topic>membranes</topic><topic>Permeabilization protocol</topic><topic>removal</topic><topic>vitelline membrane</topic><topic>Water and solids content</topic><topic>water content</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schreuders, P.D.</creatorcontrib><creatorcontrib>Kassis, J.N.</creatorcontrib><creatorcontrib>Cole, K.W.</creatorcontrib><creatorcontrib>Schneider, U.</creatorcontrib><creatorcontrib>Mahowald, A.P.</creatorcontrib><creatorcontrib>Mazur, P.</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><jtitle>Journal of insect physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schreuders, P.D.</au><au>Kassis, J.N.</au><au>Cole, K.W.</au><au>Schneider, U.</au><au>Mahowald, A.P.</au><au>Mazur, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The kinetics of embryo drying in Drosophila melanogaster as a function of the steps in permeabilization: Experimental</atitle><jtitle>Journal of insect physiology</jtitle><date>1996</date><risdate>1996</risdate><volume>42</volume><issue>5</issue><spage>501</spage><epage>516</epage><pages>501-516</pages><issn>0022-1910</issn><eissn>1879-1611</eissn><abstract>The
Drosophila embryo is surrounded by an outer chorion and an inner vitelline membrane that are an effective barrier to the movement of water. The chorion can be removed by 2.5% hypochlorite (1). If surface water is then removed by isopropanol (2), the vitelline membrane can be rendered permeable to water by heptane containing 0.3% 1-butanol (3). Here, we determined quantitatively the effects of these three steps on the permeability of the embryo to water. Permeability was assessed by exposing embryos to air at 22–23 °C and approx. 56% r.h. and determining weight loss with time. We also determined the effect of the three permeabilization steps on the water and solids contents of the embryos initially, after equilibration with air, and after complete drying. The intact embryo contains 76% (
w
w
) water and 24% solids. The successive permeabilization steps produce small increases in the former and small decreases in the latter. Intact embryos require 5–12h to lose half their water, the longer times being applicable to older embryos. After permeabilization steps (1), (1) + (2), and (1) + (2) + (3) the times for 50% water loss decrease to 1.6, 1.9, and 0.1 h, respectively.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/0022-1910(95)00122-0</doi><tpages>16</tpages></addata></record> |
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subjects | air drying body water butanol chemical treatment dechorionation Diptera Drosophila melanogaster Drosophilidae embryo (animal) Embryo dehydration embryo permeabilization embryo solids embryo water loss heptane isopropyl alcohol kinetics Membrane permeability membranes Permeabilization protocol removal vitelline membrane Water and solids content water content |
title | The kinetics of embryo drying in Drosophila melanogaster as a function of the steps in permeabilization: Experimental |
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