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2
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Inorganic Carbon Diffusion between C(4) Mesophyll and Bundle Sheath Cells: Direct Bundle Sheath CO(2) Assimilation in Intact Leaves in the Presence of an Inhibitor of the C(4) Pathway.C(4) 叶肉细胞与束鞘细胞间的无机碳扩散:在 C(4) 途径抑制剂存在的情况下完整叶片中束鞘的直接 CO(2) 同化。
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Isolation of Mesophyll Cells and Bundle Sheath Cells from Digitaria sanguinalis (L.) Scop. Leaves and a Scanning Microscopy Study of the Internal Leaf Cell Morphology.从马唐叶片中分离叶肉细胞和维管束鞘细胞以及叶片内部细胞形态的扫描显微镜研究
Plant Physiol. 1971 Jan;47(1):149-56. doi: 10.1104/pp.47.1.149.
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Spectral, Physical, and Electron Transport Activities in the Photosynthetic Apparatus of Mesophyll Cells and Bundle Sheath Cells of Digitaria sanguinalis (L.) Scop.血草(Digitaria sanguinalis (L.) Scop.)的叶肉细胞和维管束鞘细胞的光合器官中的光谱、物理和电子传递活动
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C(4) Photosynthesis: Light-dependent CO(2) Fixation by Mesophyll Cells, Protoplasts, and Protoplast Extracts of Digitaria sanguinalis.狗尾草叶肉细胞、原生质体及原生质体提取物的C(4)光合作用:光依赖型二氧化碳固定
Plant Physiol. 1975 May;55(5):835-44. doi: 10.1104/pp.55.5.835.
9
Separation of mesophyll protoplasts and bundle sheath cells from maize leaves for photosynthetic studies.从玉米叶片中分离叶肉原生质体和维管束鞘细胞用于光合研究。
Plant Physiol. 1973 Jun;51(6):1133-7. doi: 10.1104/pp.51.6.1133.
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Nitrogen Assimilation Pathways in Leaf Mesophyll and Bundle Sheath Cells of C(4) Photosynthesis Plants Formulated from Comparative Studies with Digitaria sanguinalis (L.) Scop.基于对马唐(Digitaria sanguinalis (L.) Scop.)的比较研究构建的C4光合作用植物叶肉细胞和维管束鞘细胞中的氮同化途径
Plant Physiol. 1979 Aug;64(2):309-13. doi: 10.1104/pp.64.2.309.

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Finding the C4 sweet spot: cellular compartmentation of carbohydrate metabolism in C4 photosynthesis.找到 C4 的最佳点:C4 光合作用中碳水化合物代谢的细胞区室化。
J Exp Bot. 2021 Sep 2;72(17):6018-6026. doi: 10.1093/jxb/erab290.
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Intercellular compartmentation of sucrose synthesis in leaves of Zea mays L.玉米叶片中蔗糖合成的细胞区室化
Planta. 1985 May;164(2):172-8. doi: 10.1007/BF00396079.
3
Light Modulation and Localization of Sucrose Phosphate Synthase Activity between Mesophyll Cells and Bundle Sheath Cells in C(4) Species.C4植物中叶肉细胞和维管束鞘细胞间蔗糖磷酸合酶活性的光调节与定位
Plant Physiol. 1987 Aug;84(4):1096-101. doi: 10.1104/pp.84.4.1096.
4
Mannose metabolism in corn and its impact on leaf metabolites, photosynthetic gas exchange, and chlorophyll fluorescence.玉米中的甘露糖代谢及其对叶片代谢物、光合作用气体交换和叶绿素荧光的影响。
Plant Physiol. 1986 Dec;82(4):1081-9. doi: 10.1104/pp.82.4.1081.
5
Distinction between Cytosol and Chloroplast Fructose-Bisphosphate Aldolases from Pea, Wheat, and Corn Leaves.豌豆、小麦和玉米叶片细胞质和叶绿体果糖-1,6-二磷酸醛缩酶的区别。
Plant Physiol. 1986 Feb;80(2):301-4. doi: 10.1104/pp.80.2.301.
6
Inhibition of 3-Phosphoglycerate-Dependent O(2) Evolution by Phosphoenolpyruvate in C(4) Mesophyll Chloroplasts of Digitaria sanguinalis (L.) Scop.3-磷酸甘油酸依赖性 O(2) 产生在狗牙根 C(4) 叶肉叶绿体中被磷酸烯醇丙酮酸抑制
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Starch accumulation associated with growth reduction at low temperatures in a tropical plant.淀粉积累与热带植物低温生长减缓有关。
Science. 1970 Apr 24;168(3930):494-6. doi: 10.1126/science.168.3930.494.
2
Rapid isolation of mesophyll cells from leaves of soybean for photosynthetic studies.快速分离大豆叶片中叶肉细胞用于光合作用研究。
Plant Physiol. 1977 Apr;59(4):587-90. doi: 10.1104/pp.59.4.587.
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C(4) Photosynthesis: Light-dependent CO(2) Fixation by Mesophyll Cells, Protoplasts, and Protoplast Extracts of Digitaria sanguinalis.狗尾草叶肉细胞、原生质体及原生质体提取物的C(4)光合作用:光依赖型二氧化碳固定
Plant Physiol. 1975 May;55(5):835-44. doi: 10.1104/pp.55.5.835.
4
Photosynthetic carbon metabolism in isolated maize bundle sheath strands.玉米束鞘组织片段的光合碳代谢。
Plant Physiol. 1973 Apr;51(4):787-92. doi: 10.1104/pp.51.4.787.
5
Structure and distribution of chloroplasts and other organelles in leaves with various rates of photosynthesis.不同光合作用速率叶片中叶绿体和其他细胞器的结构和分布。
Plant Physiol. 1971 Jan;47(1):15-23. doi: 10.1104/pp.47.1.15.
6
Isolation of Mesophyll Cells and Bundle Sheath Cells from Digitaria sanguinalis (L.) Scop. Leaves and a Scanning Microscopy Study of the Internal Leaf Cell Morphology.从马唐叶片中分离叶肉细胞和维管束鞘细胞以及叶片内部细胞形态的扫描显微镜研究
Plant Physiol. 1971 Jan;47(1):149-56. doi: 10.1104/pp.47.1.149.
7
COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS.分离叶绿体中的铜酶。甜菜中的多酚氧化酶。
Plant Physiol. 1949 Jan;24(1):1-15. doi: 10.1104/pp.24.1.1.
8
THE SEPARATION OF SIMPLE SUGARS BY CELLULOSE THIN-LAYER CHROMATOGRAPHY.用纤维素薄层层析法分离单糖
J Chromatogr. 1965 Feb;17:300-6. doi: 10.1016/s0021-9673(00)99872-8.
9
The C 4 -pathway of photosynthesis. Evidence for an intermediate pool of carbon dioxide and the identity of the donor C 4 -dicarboxylic acid.光合作用的C4途径。二氧化碳中间库的证据以及供体C4二羧酸的身份。
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Oxygen inhibition and other properties of soybean ribulose 1,5-diphosphate carboxylase.大豆核酮糖-1,5-二磷酸羧化酶的氧抑制作用及其他特性
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俯仰马唐离体叶细胞中的光合作用与碳水化合物代谢

Photosynthetic and Carbohydrate Metabolism in Isolated Leaf Cells of Digitaria pentzii.

作者信息

Mbaku S B, Fritz G J, Bowes G

机构信息

Departments of Agronomy and Botany, University of Florida, Gainesville, Florida 32611.

出版信息

Plant Physiol. 1978 Oct;62(4):510-5. doi: 10.1104/pp.62.4.510.

DOI:10.1104/pp.62.4.510
PMID:16660549
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1092161/
Abstract

Mesophyll cells and bundle sheath strands were isolated rapidly from leaves of the C(4) species Digitaria pentzii Stent. (slenderstem digitgrass) by a chopping and differential filtration technique. Rates of CO(2) fixation in the light by mesophyll and bundle sheath cells without added exogenous substrates were 6.3 and 54.2 micromoles of CO(2) per milligram of chlorophyll per hour, respectively. The addition of pyruvate or phosphoenolpyruvate to the mesophyll cells increased the rates to 15.2 and 824.6 micromoles of CO(2) per milligram of chlorophyll per hour, respectively. The addition of ribose 5-phosphate increased the rate for bundle sheath cells to 106.8 micromoles of CO(2) per milligram of chlorophyll per hour. These rates are comparable to those reported for cells isolated by other methods. The K(m)(HCO(3) (-)) for mesophyll cells was 0.9 mm; for bundle sheath cells it was 1.3 mm at low, and 40 mm at higher HCO(3) (-) concentrations. After 2 hours of photosynthesis by mesophyll cells in (14)CO(2) and phosphoenolpyruvate, 88% of the incorporated (14)C was found in organic acids and 0.8% in carbohydrates; for bundle sheath cells incubated in ribose 5-phosphate and ATP, more than 58% of incorporated (14)C was found in carbohydrates, mainly starch, and 32% in organic acids. These findings, together with the stimulation of CO(2) fixation by phosphoenolpyruvate for mesophyll cells and by ribose 5-phosphate plus ATP for bundle sheath cells, and the location of phosphoenolpyruvate and ribulose bisphosphate carboxylases in mesophyll and bundle sheath cells, respectively, are in accord with the scheme of C(4) photosynthesis which places the Calvin cycle in the bundle sheath and C(4) acid formation in mesophyll cells.Starch and reducing sugars were present in both mesophyll and bundle sheath cells following a period of photosynthesis by whole leaves. However, when isolated cells were exposed to (14)CO(2) in the light, even with appropriate exogenous substrates, only bundle sheath cells accumulated appreciable amounts of labeled carbohydrates. Incubation of mesophyll cells in the light with ATP and either pyruvate and inorganic phosphate, or phosphoenolpyruvate, or 3-phosphoglycerate resulted in large increases in total carbohydrates. The 3-phosphoglycerate treatment produced the greatest increase. These results could not be explained on the basis of increased CO(2) fixation. They suggest that mesophyll cells are able to metabolize exogenously supplied 3-carbon compounds to carbohydrates, despite the apparent inability of these cells to utilize CO(2) for this purpose, and support the view that in the whole leaf 3-phosphoglycerate is transported from bundle sheath to mesophyll cells, where it is reduced to carbohydrate.Sucrose and sucrose-phosphate synthetases and invertase were localized mainly in bundle sheath cells. ADP-Glucose starch synthetase and amylase were present mainly in bundle sheath cells whereas starch phosphorylase was present mainly in mesophyll cells.

摘要

采用切碎和差速过滤技术,从C4植物纤细臂形草(Digitaria pentzii Stent.)的叶片中快速分离出叶肉细胞和维管束鞘细胞。在不添加外源底物的情况下,叶肉细胞和维管束鞘细胞在光照下固定CO₂的速率分别为每毫克叶绿素每小时6.3微摩尔和54.2微摩尔。向叶肉细胞中添加丙酮酸或磷酸烯醇丙酮酸后,固定速率分别提高到每毫克叶绿素每小时15.2微摩尔和824.6微摩尔。向维管束鞘细胞中添加5-磷酸核糖后,固定速率提高到每毫克叶绿素每小时106.8微摩尔。这些速率与通过其他方法分离的细胞所报道的速率相当。叶肉细胞的K(m)(HCO₃⁻)为0.9毫米;维管束鞘细胞在低HCO₃⁻浓度下为l.3毫米,在较高HCO₃⁻浓度下为40毫米。叶肉细胞在¹⁴CO₂和磷酸烯醇丙酮酸中进行2小时光合作用后,88%的掺入¹⁴C存在于有机酸中,0.8%存在于碳水化合物中;对于在5-磷酸核糖和ATP中孵育的维管束鞘细胞,超过58%的掺入¹⁴C存在于碳水化合物中,主要是淀粉,32%存在于有机酸中。这些发现,连同磷酸烯醇丙酮酸对叶肉细胞CO₂固定的刺激作用以及5-磷酸核糖加ATP对维管束鞘细胞的刺激作用,以及磷酸烯醇丙酮酸羧化酶和核酮糖二磷酸羧化酶分别在叶肉细胞和维管束鞘细胞中的定位,都与C₄光合作用的模式一致,即卡尔文循环发生在维管束鞘中,C₄酸形成于叶肉细胞中。在全叶进行一段时间光合作用后,叶肉细胞和维管束鞘细胞中都存在淀粉和还原糖。然而,当分离的细胞在光照下暴露于¹⁴CO₂时,即使有合适的外源底物,只有维管束鞘细胞积累了可观数量的标记碳水化合物。叶肉细胞在光照下与ATP以及丙酮酸和无机磷酸、或磷酸烯醇丙酮酸、或3-磷酸甘油酸一起孵育,导致总碳水化合物大量增加。3-磷酸甘油酸处理产生的增加最大。这些结果不能用CO₂固定增加来解释。它们表明,尽管这些细胞显然不能利用CO₂来合成碳水化合物,但叶肉细胞能够将外源供应的三碳化合物代谢为碳水化合物,并支持这样一种观点,即在全叶中,3-磷酸甘油酸从维管束鞘运输到叶肉细胞,在那里它被还原为碳水化合物。蔗糖和蔗糖磷酸合成酶以及转化酶主要定位于维管束鞘细胞中。ADP-葡萄糖淀粉合成酶和淀粉酶主要存在于维管束鞘细胞中,而淀粉磷酸化酶主要存在于叶肉细胞中。