Pub Date : 1992-11-01DOI: 10.1016/S0015-3796(11)80026-0
Yao-Hua Luo
Carbon dioxide evolved by CAM plants (Aloe vera, Neoregelia sp. Sansevieria guineensis) in light (δ13C = 0.8 ± 1.8%) was significantly enriched in 13C relative to that in dark (δ13C = -13.0 ± 1.4%). The changes in S 13C values of CO2 with light intensity revealed curves similar to those of photosynthetic rate versus light. The ratio of the amount of collected CO2 Cc over the amount of malic acid consumed (Cm) declined sharply from low light to about 95 µmol m−2 s−1. Thereafter, this decline tended to be slow. The δ13C values of CO2 evolved versus the corresponding Cc/Cm were linearly correlated, showing different slopes for each species, which is consistent with the expectations of the model established in this study. The yields of carbon dioxide for each malic acid decarboxylated evaluated from the model equation, termed N, were 3.0, 1.5, and 1.3 for S. guineensis, A. vera, Neoregelia sp., respectively.
{"title":"Changes in 13C/12C Ratio of CO2 Evolved from CAM Plants with Light Intensities in Relation to Malic Acid Decarboxylation","authors":"Yao-Hua Luo","doi":"10.1016/S0015-3796(11)80026-0","DOIUrl":"10.1016/S0015-3796(11)80026-0","url":null,"abstract":"<div><p>Carbon dioxide evolved by CAM plants (Aloe vera, Neoregelia sp. Sansevieria guineensis) in light (δ13C = 0.8 ± 1.8%) was significantly enriched in <sup>13</sup>C relative to that in dark (δ13C = -13.0 ± 1.4%). The changes in S 13C values of CO2 with light intensity revealed curves similar to those of photosynthetic rate versus light. The ratio of the amount of collected CO<sub>2</sub> C<sub>c</sub> over the amount of malic acid consumed (C<sub>m</sub>) declined sharply from low light to about 95 µmol m<sup>−2</sup> s<sup>−1</sup>. Thereafter, this decline tended to be slow. The δ<sup>13</sup>C values of CO<sub>2</sub> evolved versus the corresponding C<sub>c</sub>/C<sub>m</sub> were linearly correlated, showing different slopes for each species, which is consistent with the expectations of the model established in this study. The yields of carbon dioxide for each malic acid decarboxylated evaluated from the model equation, termed N, were 3.0, 1.5, and 1.3 for S. guineensis, <em>A. vera, Neoregelia</em> sp., respectively.</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 4","pages":"Pages 221-229"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80026-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89952957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-11-01DOI: 10.1016/S0015-3796(11)80034-X
R.B. Myneni, J. Ross
{"title":"","authors":"R.B. Myneni, J. Ross","doi":"10.1016/S0015-3796(11)80034-X","DOIUrl":"10.1016/S0015-3796(11)80034-X","url":null,"abstract":"","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 4","pages":"Page 272"},"PeriodicalIF":0.0,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80034-X","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"113553429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-07-01DOI: 10.1016/S0015-3796(11)80001-6
Fumiko Sato , Hiroshi Ashihara
Maximum activities of phosphofructokinase (PFK), PPi: fructose-6-phosphate 1-phosphotransferase (PFP) and fructose- 1,6-bisphosphatase (FBPase) were determined in desalted extracts from gluconeogenic and non-gluconeogenic tissues from seedlings of peanut, safflower, black gram, green gram, radish and buckwheat. FBPase activity was high only in gluconeogenic tissues, but PFP activity was distributed at significant levels in all tissues examined. PFP activity was always higher than PFK activity. In normal and γ-irradiated peanut cotyledons, the changing pattern of activity of FBPase after germination, but not that of PFP, resembled the changing pattern of gluconeogenic capacity, as estimated by the incorporation of [2-14C]glycerol to sugars. The minor role of PFP in gluconeogenesis in germinating fatty seeds is discussed.
{"title":"Pyrophosphate: Fructose-6-phosphate Phosphotransferase and Gluconeogenic Capacity in Germinated Peanut Seeds","authors":"Fumiko Sato , Hiroshi Ashihara","doi":"10.1016/S0015-3796(11)80001-6","DOIUrl":"10.1016/S0015-3796(11)80001-6","url":null,"abstract":"<div><p>Maximum activities of phosphofructokinase (PFK), PPi: fructose-6-phosphate 1-phosphotransferase (PFP) and fructose- 1,6-bisphosphatase (FBPase) were determined in desalted extracts from gluconeogenic and non-gluconeogenic tissues from seedlings of peanut, safflower, black gram, green gram, radish and buckwheat. FBPase activity was high only in gluconeogenic tissues, but PFP activity was distributed at significant levels in all tissues examined. PFP activity was always higher than PFK activity. In normal and γ-irradiated peanut cotyledons, the changing pattern of activity of FBPase after germination, but not that of PFP, resembled the changing pattern of gluconeogenic capacity, as estimated by the incorporation of [2-<sup>14</sup>C]glycerol to sugars. The minor role of PFP in gluconeogenesis in germinating fatty seeds is discussed.</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Pages 145-151"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80001-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79301259","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Polyamines can be considered as a new class of plant growth regulators. However to be considered as hormones, they have to respond to the translocatability criterion in the whole plant. The results presented here show that a small droplet (10 µl) of 14C-putrescine supplied to a source leaf is redistributed to the whole plant. Long-distance transport occurs mainly towards young growing organs (apex, roots, stolons, tubers). Bidirectional translocation, which is also found is a result of interactions between the attractive strengths of different sinks. Heat girdling of shoots induces a strong inhibition of transport which suggests transport via the phloem. Other data, such as non labeling of mature leaves, normally fed by xylem flux and the higher content (4 to 10 times) of endogenous PAs in phloem exudate compared with xylem exudate confirm this conclusion. After a 3 h period of transport, separation of labelled compounds by thin layer chromatography shows that the radioactivity supplied as 14C-putrescine is found as putrescine (from 64% to 82%), spermidine (from 14% to 28%) and spermine (3%) depending on the organ. This indicates that there is no important degradation of putrescine before it reaches the transport pathway.
{"title":"Long Distance Transport of 14C-Putrescine in Potato Plantlets (Solanum tuberosum cv. Bintje)","authors":"Jacky Beraud, Andrlé Brun, Annie Feray, Annick Hourmant , Michel Penot","doi":"10.1016/S0015-3796(11)80004-1","DOIUrl":"10.1016/S0015-3796(11)80004-1","url":null,"abstract":"<div><p>Polyamines can be considered as a new class of plant growth regulators. However to be considered as hormones, they have to respond to the translocatability criterion in the whole plant. The results presented here show that a small droplet (10 µl) of <sup>14</sup>C-putrescine supplied to a source leaf is redistributed to the whole plant. Long-distance transport occurs mainly towards young growing organs (apex, roots, stolons, tubers). Bidirectional translocation, which is also found is a result of interactions between the attractive strengths of different sinks. Heat girdling of shoots induces a strong inhibition of transport which suggests transport via the phloem. Other data, such as non labeling of mature leaves, normally fed by xylem flux and the higher content (4 to 10 times) of endogenous PA<sub>s</sub> in phloem exudate compared with xylem exudate confirm this conclusion. After a 3 h period of transport, separation of labelled compounds by thin layer chromatography shows that the radioactivity supplied as <sup>14</sup>C-putrescine is found as putrescine (from 64% to 82%), spermidine (from 14% to 28%) and spermine (3%) depending on the organ. This indicates that there is no important degradation of putrescine before it reaches the transport pathway.</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Pages 169-176"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80004-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77549533","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-07-01DOI: 10.1016/S0015-3796(11)80005-3
Zdenko Rengel , Daphne C. Elliott
Calcium ions serve as a second messenger in the transduction of environmental and hormonal signals to the responsive elements of cell metabolism. Effects of Al on the cell Ca2+ homeostasis remain to be elucidated. Short-term net 45Ca2+ uptake by Amaranthus tricolor protoplasts was measured in media prepared to test the influence of various buffers, pH values, Ca2+ and Al concentrations. A modified GEOCHEM program was used to calculate activities of Ca2+ and all monomeric Al species. Net 45Ca2+ uptake was smaller at pH 4.5 compared to uptake at pH 5.5 and increased linearly with an increase in Ca2+ activity in the uptake media from 0.23 to 2.0 mM. Aluminium caused a significant decrease in net 45Ca2+ uptake. This Al-related decrease was less expressed at higher Ca2+ activities. Summed activities of monomeric Al species (Al3+ and hydroxy-Al) were significantly related to the reduction of net 45Ca2+ uptake. The equilibrium constant (Ki) of the reversible association of the Ca2+ membrane-transporter and monomeric Al species was calculated from Dixon plots to be equivalent to 4 and 30 micromolar activity of total monomeric Al for uptake media with pH values of 4.5 and 5.5, respectively. It is suggested that the primary Al effects are generally exerted through reducing inward Ca2+ fluxes across the plasma membrane.
{"title":"Aluminium Inhibits Net 45Ca2+ Uptake by Amaranthus Protoplasts","authors":"Zdenko Rengel , Daphne C. Elliott","doi":"10.1016/S0015-3796(11)80005-3","DOIUrl":"10.1016/S0015-3796(11)80005-3","url":null,"abstract":"<div><p>Calcium ions serve as a second messenger in the transduction of environmental and hormonal signals to the responsive elements of cell metabolism. Effects of Al on the cell Ca<sup>2+</sup> homeostasis remain to be elucidated. Short-term net <sup>45</sup>Ca<sup>2+</sup> uptake by <em>Amaranthus tricolor</em> protoplasts was measured in media prepared to test the influence of various buffers, <em>p</em>H values, Ca<sup>2+</sup> and Al concentrations. A modified GEOCHEM program was used to calculate activities of Ca<sup>2+</sup> and all monomeric Al species. Net <sup>45</sup>Ca<sup>2+</sup> uptake was smaller at <em>p</em>H 4.5 compared to uptake at <em>p</em>H 5.5 and increased linearly with an increase in Ca<sup>2+</sup> activity in the uptake media from 0.23 to 2.0 mM. Aluminium caused a significant decrease in net <sup>45</sup>Ca<sup>2+</sup> uptake. This Al-related decrease was less expressed at higher Ca<sup>2+</sup> activities. Summed activities of monomeric Al species (Al<sup>3+</sup> and hydroxy-Al) were significantly related to the reduction of net <sup>45</sup>Ca<sup>2+</sup> uptake. The equilibrium constant (Ki) of the reversible association of the Ca<sup>2+</sup> membrane-transporter and monomeric Al species was calculated from Dixon plots to be equivalent to 4 and 30 micromolar activity of total monomeric Al for uptake media with <em>p</em>H values of 4.5 and 5.5, respectively. It is suggested that the primary Al effects are generally exerted through reducing inward Ca<sup>2+</sup> fluxes across the plasma membrane.</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Pages 177-186"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80005-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85196611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Proteins of healthy pea plants (Pisum sativum L. cv. Nadja) and of plants infected with red clover mottle virus were examined by one- and two-dimensional electrophoresis.
Silver-stained 2-D slab gels revealed more than ten additional protein spots with markedly changed intensity in the extracts from infected plants as compared to extracts from uninfected plants. Two of these spots corresponded to virus proteins (about 38 and 21 kDa).
健康豌豆植株(Pisum sativum L. cv.)的蛋白质。采用单、双向电泳法对红三叶草斑驳病毒侵染植物进行了检测。银染二维平板凝胶显示,与未感染植物的提取物相比,感染植物的提取物中有10多个额外的蛋白质斑点,其强度显著改变。其中两个点对应于病毒蛋白(约38和21 kDa)。
{"title":"Changes in Protein Patterns of Pea Plants Systemically Infected with Red Clover Mottle Virus","authors":"Kamil Marcinka , Cornelia Röhring , Siegfried Kluge","doi":"10.1016/S0015-3796(11)80006-5","DOIUrl":"10.1016/S0015-3796(11)80006-5","url":null,"abstract":"<div><p>Proteins of healthy pea plants (<em>Pisum sativum</em> L. cv. Nadja) and of plants infected with red clover mottle virus were examined by one- and two-dimensional electrophoresis.</p><p>Silver-stained 2-D slab gels revealed more than ten additional protein spots with markedly changed intensity in the extracts from infected plants as compared to extracts from uninfected plants. Two of these spots corresponded to virus proteins (about 38 and 21 kDa).</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Pages 187-193"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80006-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75230112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-07-01DOI: 10.1016/S0015-3796(11)80009-0
G. Sembdner
{"title":"","authors":"G. Sembdner","doi":"10.1016/S0015-3796(11)80009-0","DOIUrl":"10.1016/S0015-3796(11)80009-0","url":null,"abstract":"","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Page 204"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80009-0","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86408090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-07-01DOI: 10.1016/S0015-3796(11)80002-8
Yonezo Suzuki , Manami Yoshishige
A sensitive and comparatively simple spectrophotometric method for the assay of meso-diaminopimelic acid decarboxylase is presented. It is based upon the coupled reaction of the decarboxylase with pea diamine oxidase and horseradish peroxidase.L-Lysine, a product of meso-diaminopimelic acid decarboxylase is oxidized by pea diamine oxidase and the hydrogen peroxide generated is estimated as the red colour (quinoneimine dye) formed on the peroxidative oxidation of the mixture of 3,5-dichloro-2-hydroxybenzenesulfonate and 4-aminoantipyrine. The method was compared with the result by a high performance liquid chromatography assay.
{"title":"Spectrophotometric Assay for Diaminopimelate Decarboxylase of Higher Plants using Pea Diamine Oxidase","authors":"Yonezo Suzuki , Manami Yoshishige","doi":"10.1016/S0015-3796(11)80002-8","DOIUrl":"10.1016/S0015-3796(11)80002-8","url":null,"abstract":"<div><p>A sensitive and comparatively simple spectrophotometric method for the assay of <em>meso</em>-diaminopimelic acid decarboxylase is presented. It is based upon the coupled reaction of the decarboxylase with pea diamine oxidase and horseradish peroxidase.L-Lysine, a product of <em>meso</em>-diaminopimelic acid decarboxylase is oxidized by pea diamine oxidase and the hydrogen peroxide generated is estimated as the red colour (quinoneimine dye) formed on the peroxidative oxidation of the mixture of 3,5-dichloro-2-hydroxybenzenesulfonate and 4-aminoantipyrine. The method was compared with the result by a high performance liquid chromatography assay.</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Pages 153-159"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80002-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82040060","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-07-01DOI: 10.1016/S0015-3796(11)80011-9
U. Schiewer
{"title":"","authors":"U. Schiewer","doi":"10.1016/S0015-3796(11)80011-9","DOIUrl":"https://doi.org/10.1016/S0015-3796(11)80011-9","url":null,"abstract":"","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Page 206"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80011-9","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137191013","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1992-07-01DOI: 10.1016/S0015-3796(11)80007-7
Gottfried Schuster
Ethionine markedly inhibits the replication of potato virus X (PVX) after infiltration into leaf disks of Nicotiana tabacum L. “Samsun”. P-fluorophenylalanine and 5-methyl-DL-tryptophane inhibit this replication less effectively and only at phytotoxic concentrations. Methionine strongly reduces the inhibitory activity of ethionine in the replication of PVX. In leaf disks with synchronized virus infection, the time-response course of ethionine inhibition indicates that a late event is inhibited. Short time after the beginning of ethionine inhibition decline virus protein was detected by ELISA. Contrary to leaf disks, in intact tobacco plants PVX replication is inhibited by ethionine sprays only in very high and phytotoxic doses. However, low doses of ethionine increase synergistically the inhibitory activity of 5-azadihydrouracil.
{"title":"Investigations on the Inhibition of Potato Virus X by Some Amino Acid Analogues","authors":"Gottfried Schuster","doi":"10.1016/S0015-3796(11)80007-7","DOIUrl":"10.1016/S0015-3796(11)80007-7","url":null,"abstract":"<div><p>Ethionine markedly inhibits the replication of potato virus X (PVX) after infiltration into leaf disks of <em>Nicotiana tabacum</em> L. “Samsun”. P-fluorophenylalanine and 5-methyl-DL-tryptophane inhibit this replication less effectively and only at phytotoxic concentrations. Methionine strongly reduces the inhibitory activity of ethionine in the replication of PVX. In leaf disks with synchronized virus infection, the time-response course of ethionine inhibition indicates that a late event is inhibited. Short time after the beginning of ethionine inhibition decline virus protein was detected by ELISA. Contrary to leaf disks, in intact tobacco plants PVX replication is inhibited by ethionine sprays only in very high and phytotoxic doses. However, low doses of ethionine increase synergistically the inhibitory activity of 5-azadihydrouracil.</p></div>","PeriodicalId":8798,"journal":{"name":"Biochemie und Physiologie der Pflanzen","volume":"188 3","pages":"Pages 195-201"},"PeriodicalIF":0.0,"publicationDate":"1992-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0015-3796(11)80007-7","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81365783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}