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在高光和低光条件下生长的白芥菜类囊体中锰的测量。

Measurements of manganese in thylakoids of Sinapis alba grown under high-light and low-light conditions.

机构信息

Institut für Allgemelne Botanik der Universität Mainz, Saarstr. 21, D-6500, Mainz, Federal Republic of Germany.

出版信息

Photosynth Res. 1981 Jun;2(2):105-14. doi: 10.1007/BF00028751.

DOI:10.1007/BF00028751
PMID:24470201
Abstract

The manganese content of thylakoids and tissues was measured in leaves grown under high- and low-light conditions. Especially when grown in a nutrient medium enriched in manganese (20 μM), the thylakoids contained large amounts of manganese, which could be removed by EDTA washing without impairment of the Hill reaction. The unremovable content of manganese was almost the same in thylakoids from plants grown in nutrient media of normal (2 μM) and reduced (0.2 μM) manganese content. Up to this limit of manganese content, Hill activity did not seem to be impaired. 1.2 atoms Mn per 100 molecules chlorophyll were found in low-light thylakoids and 1.6 atoms Mn in high-light thylakoids. This is similar to the behaviour of other electron transport components, the number of which is also decreased under low-light conditions. However, the decrease in the manganese content is not as striking as the decrease in, for example, the cytochrome f and ferredoxin content. This may be attributed to an invariable pool of manganese which is not involved in the oxygen evolving system. Alternatively, if all of our measured manganese is involved in electron transport to PS II, this could indicate that in low-light chloroplasts the ratio of PS II/PS I components may be somewhat increased.

摘要

在高光和低光条件下生长的叶片中测量了类囊体和组织中的锰含量。特别是在富含锰(20 μM)的营养培养基中生长时,类囊体中含有大量的锰,可以通过 EDTA 洗涤除去,而不会损害希尔反应。在正常(2 μM)和低(0.2 μM)锰含量的营养培养基中生长的植物类囊体中,不可去除的锰含量几乎相同。在锰含量达到这个限度之前,希尔活性似乎没有受到损害。在低光下的类囊体中发现每 100 个叶绿素分子中有 1.2 个锰原子,在高光下的类囊体中有 1.6 个锰原子。这与其他电子传递成分的行为相似,其数量在低光条件下也减少了。然而,锰含量的减少并不像细胞色素 f 和铁氧还蛋白含量的减少那样引人注目。这可能归因于不参与产氧系统的锰不变池。或者,如果我们测量的所有锰都参与 PS II 的电子传递,这可能表明在低光下叶绿体中 PS II/PSI 成分的比例可能会略有增加。

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本文引用的文献

1
[Investigations on the distribution of manganese between cell fractions from spinach leaves].[菠菜叶细胞组分间锰分布的研究]
Planta. 1968 Sep;79(3):235-48. doi: 10.1007/BF00396030.
2
Measurements of cytochrome f and P-700 in intact leaves of Sinapis alba grown under high-light and low-light conditions.在高光和低光条件下生长的白芥完整叶片中叶细胞色素 f 和 P-700 的测量。
Planta. 1979 Sep;146(4):377-85. doi: 10.1007/BF00380848.
3
Photosynthetic apparatus in chilling-sensitive plants : VI. Cold and dark-induced changes in chloroplast superoxide dismutase activity in relation to loosely-bound manganese content.
冷敏植物的光合作用器官:六、叶绿体超氧化物歧化酶活性与松散结合锰含量在冷和暗诱导下的变化关系。
Planta. 1979 Jan;145(2):145-50. doi: 10.1007/BF00388710.
4
Manganese superoxide dismutase from a higher plant : Purification of a new Mn-containing enzyme.高等植物的锰超氧化物歧化酶:一种新含锰酶的纯化。
Planta. 1980 Jan;150(2):153-7. doi: 10.1007/BF00582359.
5
A rapid technique for isolating chloroplasts with high rates of endogenous photophosphorylation.一种快速分离具有高内源性光合磷酸化率的叶绿体的技术。
Plant Physiol. 1967 Oct;42(10):1389-94. doi: 10.1104/pp.42.10.1389.
6
Studies on the manganese of the chloroplast.叶绿体锰的研究。
Plant Physiol. 1967 Jul;42(7):997-1007. doi: 10.1104/pp.42.7.997.
7
Stoichiometry of system I and system II reaction centers and of plastoquinone in different photosynthetic membranes.不同光合膜中Ⅰ型和Ⅱ型反应中心及质体醌的化学计量。
Proc Natl Acad Sci U S A. 1980 Aug;77(8):4712-6. doi: 10.1073/pnas.77.8.4712.
8
Sites of function of manganese within photosystem II. Roles in O2 evolution and system II.锰在光系统II中的功能位点。在氧气释放及光系统II中的作用。
Biochim Biophys Acta. 1970 Mar 3;197(2):219-39. doi: 10.1016/0005-2728(70)90033-2.
9
Manganese in photosynthetic oxygen evolution. I. Electron paramagnetic resonance study of the environment of manganese in Tris-washed chloroplasts.光合作用放氧过程中的锰。I. 三羟甲基氨基甲烷洗涤过的叶绿体中锰环境的电子顺磁共振研究。
Biochim Biophys Acta. 1974 Aug 23;357(2):252-66. doi: 10.1016/0005-2728(74)90065-6.
10
Two electron donation sites for exogenous reductants in chloroplast photosystem II.叶绿体光系统II中两个用于外源还原剂的电子供体位点。
Biochim Biophys Acta. 1975 Jul 8;396(1):48-62. doi: 10.1016/0005-2728(75)90188-7.