Literature DB >> 16662544

Influence of Nitrate and Ammonia on Photosynthetic Characteristics and Leaf Anatomy of Moricandia arvensis.

K Winter1, H Usuda, M Tsuzuki, M Schmitt, G E Edwards, R J Thomas, R F Evert.   

Abstract

The leaf anatomy and certain photosynthetic properties of nitrate- and ammonia-grown plants of Moricandia arvensis (L.) DC., a species previously reported to be a C(3)-C(4) intermediate, were investigated. Nitrate-grown plants had a high level of malate in the leaves while ammonia-grown plants had low levels of malate. In young leaves of nitrate-grown plants, there was a diurnal fluctuation of malate content, increasing during the day and decreasing during the night. Titratable acidity remained low in leaves of both nitrate- and ammonia-grown plants.In nitrate-grown plants, the activity of phosphoenolpyruvate (PEP) carboxylase was about 2-fold higher than in ammonia-grown plants, the latter having activity typical of C(3) species. Also, in nitrate-grown plants, the ratio of activities of ribulose 1,5-bisphosphate (RuBP) carboxylase/PEP carboxylase was lower than in ammonia-grown plants. Nitrate reductase activities were higher in nitrate- than in ammonia-grown plants and the greatest activity was found in younger leaves.With nitrate-grown plants, during a pulse-chase experiment the label in malate, as a percentage of the total labeled products, increased from about 7% after a 10-second pulse with (14)CO(2) up to 17% during a 5-minute chase with (12)CO(2). The pattern of (14)C labeling in various metabolites suggests the primary carboxylation is through RuBP carboxylase with a secondary carboxylation through PEP carboxylase. In similar experiments, with ammonia-grown plants, the percentage label in malate was only 0% to 4% with no increase in malate labeling during the chase period. The CO(2) compensation point was lower in nitrate-grown than ammonia-grown plants.There was no evidence of Kranz-like anatomy in either the nitrate or ammonia-grown plants. Mitochondria of bundle-sheath cells were strikingly positioned along the inner tangential wall. This might allow the chloroplasts of these cells to fix the mitochondrial photorespired CO(2) more effectively and contribute to the low CO(2) compensation point in the species. Chloroplasts of bundle-sheath cells and contiguous mesophyll cells were similar in size and structure in plants grown on different media, although chloroplast thylakoids and stromata of the ammonia-grown plants stained more intensely than those of nitrate-grown plants. In addition, irregular clusters of phytoferritin particles occurred in the chloroplasts of the ammonia-grown plants.The results indicate that the substantial activity of PEP carboxylase, incorporation of CO(2) into malate, the high malate content, and in part the relatively low CO(2) compensation point in Moricandia arvensis may be accounted for by metabolism of nitrate rather than by a state of C(3)-C(4) intermediacy.

Entities:  

Year:  1982        PMID: 16662544      PMCID: PMC1067198          DOI: 10.1104/pp.70.2.616

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  15 in total

1.  COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS.

Authors:  D I Arnon
Journal:  Plant Physiol       Date:  1949-01       Impact factor: 8.340

2.  Carbon Dioxide and Water Vapor Exchange in the Crassulacean Acid Metabolism Plant Kalanchoë pinnáta during a Prolonged Light Period: METABOLIC AND STOMATAL CONTROL OF CARBON METABOLISM.

Authors:  K Winter
Journal:  Plant Physiol       Date:  1980-11       Impact factor: 8.340

3.  Day/Night Changes in the Sensitivity of Phosphoenolpyruvate Carboxylase to Malate during Crassulacean Acid Metabolism.

Authors:  K Winter
Journal:  Plant Physiol       Date:  1980-05       Impact factor: 8.340

4.  Studies on the mechanism of glycerate 3-phosphate synthesis in tomato and maize leaves.

Authors:  J M Galmiche
Journal:  Plant Physiol       Date:  1973-03       Impact factor: 8.340

5.  Differential Oxygen Response of Photosynthesis in Soybean and Panicum milioides.

Authors:  R W Keck
Journal:  Plant Physiol       Date:  1976-10       Impact factor: 8.340

6.  Occurrence of Pyruvate Orthophosphate Dikinase in the Succulent Plant, Kalanchoë daigremontiana Hamet. et. Perr.

Authors:  T Sugiyama
Journal:  Plant Physiol       Date:  1975-11       Impact factor: 8.340

7.  Effects of Light, Carbon Dioxide, and Temperature on Photosynthesis, Oxygen Inhibition of Photosynthesis, and Transpiration in Solanum tuberosum.

Authors:  S B Ku; G E Edwards; C B Tanner
Journal:  Plant Physiol       Date:  1977-05       Impact factor: 8.340

8.  Ionic balance in different tissues of the tomato plant in relation to nitrate, urea, or ammonium nutrition.

Authors:  E A Kirkby; K Mengel
Journal:  Plant Physiol       Date:  1967-01       Impact factor: 8.340

9.  Photosynthetic CO(2) Fixation Products and Activities of Enzymes Related to Photosynthesis in Bermudagrass and Other Plants.

Authors:  T M Chen; R H Brown; C C Black
Journal:  Plant Physiol       Date:  1971-02       Impact factor: 8.340

10.  Carbon dioxide compensation points of flowering plants.

Authors:  E G Krenzer; D N Moss; R K Crookston
Journal:  Plant Physiol       Date:  1975-08       Impact factor: 8.340

View more
  23 in total

1.  Photosynthetic/photorespiratory characteristics of C3-C 4 intermediate species.

Authors:  A S Holaday; R Chollet
Journal:  Photosynth Res       Date:  1984-12       Impact factor: 3.573

Review 2.  Russ Monson and the evolution of C4 photosynthesis.

Authors:  Rowan F Sage
Journal:  Oecologia       Date:  2021-03-04       Impact factor: 3.225

3.  C(3)-C(4) Intermediate Species in Alternanthera (Amaranthaceae) : Leaf Anatomy, CO(2) Compensation Point, Net CO(2) Exchange and Activities of Photosynthetic Enzymes.

Authors:  G Rajendrudu; J S Prasad; V S Das
Journal:  Plant Physiol       Date:  1986-02       Impact factor: 8.340

4.  C3-C 4 Intermediate species in the genus Flaveria: leaf anatomy, ultrastructure, and the effect of O2 on the CO 2 compensation concentration.

Authors:  A S Holaday; K W Lee; R Chollet
Journal:  Planta       Date:  1984-01       Impact factor: 4.116

5.  Nitrogen Source Regulation of Growth and Photosynthesis in Beta vulgaris L.

Authors:  T. K. Raab; N. Terry
Journal:  Plant Physiol       Date:  1994-08       Impact factor: 8.340

6.  Carbon Partitioning in a Flaveria linearis Mutant with Reduced Cytosolic Fructose Bisphosphatase.

Authors:  T D Sharkey; L V Savitch; P J Vanderveer; B J Micallef
Journal:  Plant Physiol       Date:  1992-09       Impact factor: 8.340

7.  A model of photosynthetic CO2 assimilation and carbon-isotope discrimination in leaves of certain C3-C 4 intermediates.

Authors:  S von Caemmerer
Journal:  Planta       Date:  1989-12       Impact factor: 4.116

8.  Gas-exchange of ears of cereals in response to carbon dioxide and light : II. Occurrence of a C3-C 4 intermediate type of photosynthesis.

Authors:  A Ziegler-Jöns
Journal:  Planta       Date:  1989-05       Impact factor: 4.116

9.  Carbon, Nitrogen, and Nutrient Interactions in Beta vulgaris L. as Influenced by Nitrogen Source, NO3- versus NH4+

Authors:  T. K. Raab; N. Terry
Journal:  Plant Physiol       Date:  1995-02       Impact factor: 8.340

10.  Co-function of C3-and C 4-photosynthetic pathways in C3, C 4 and C 3-C 4 intermediate Flaveria species.

Authors:  R K Monson; B D Moore; M S Ku; G E Edwards
Journal:  Planta       Date:  1986-09       Impact factor: 4.116

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.