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Changes in photosynthetic carbon flow in transgenic rice plants that express C4-type phosphoenolpyruvate carboxykinase from Urochloa panicoides.表达来自类蜀黍的C4型磷酸烯醇式丙酮酸羧化激酶的转基因水稻植株光合碳流的变化。
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Efficient selection of somatic hybrids in Nicotiana tabacum L. using a combination of drug-resistance markers introduced by transformation.利用转化引入的耐药性标记物组合高效选择烟草体细胞杂种。
Theor Appl Genet. 1989 Apr;77(4):547-52. doi: 10.1007/BF00274277.
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Phosphoenolpyruvate carboxykinase in plants exhibiting crassulacean Acid metabolism.具有景天酸代谢途径的植物中的磷酸烯醇式丙酮酸羧激酶。
Plant Physiol. 1973 Oct;52(4):357-61. doi: 10.1104/pp.52.4.357.
3
The role of phosphoenolpyruvate carboxykinase in a marine macroalga with C4-like photosynthetic characteristics.磷酸烯醇式丙酮酸羧激酶在具有类C4光合特征的海洋大型藻类中的作用。
Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2883-7. doi: 10.1073/pnas.88.7.2883.
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Characterization of the gene family for alternative oxidase from Arabidopsis thaliana.拟南芥交替氧化酶基因家族的特征分析
Plant Mol Biol. 1997 Nov;35(5):585-96. doi: 10.1023/a:1005818507743.
5
Phosphorylation of phosphoenolpyruvate carboxykinase in plants. Studies in plants with C4 photosynthesis and Crassulacean acid metabolism and in germinating seeds.植物中磷酸烯醇式丙酮酸羧激酶的磷酸化。对具有C4光合作用和景天酸代谢的植物以及萌发种子的研究。
Biochem J. 1996 Aug 1;317 ( Pt 3)(Pt 3):653-8. doi: 10.1042/bj3170653.
6
Crystal structure of Escherichia coli phosphoenolpyruvate carboxykinase: a new structural family with the P-loop nucleoside triphosphate hydrolase fold.大肠杆菌磷酸烯醇丙酮酸羧激酶的晶体结构:具有P环核苷三磷酸水解酶折叠的新结构家族。
J Mol Biol. 1996 Feb 16;256(1):126-43. doi: 10.1006/jmbi.1996.0072.
7
Characterization of the expression of a desiccation-responsive rd29 gene of Arabidopsis thaliana and analysis of its promoter in transgenic plants.拟南芥脱水响应rd29基因的表达特征及其在转基因植物中的启动子分析。
Mol Gen Genet. 1993 Jan;236(2-3):331-40. doi: 10.1007/BF00277130.
8
Cloning and characterization of the gene encoding ATP-dependent phospho-enol-pyruvate carboxykinase in Trypanosoma cruzi: comparison of primary and predicted secondary structure with host GTP-dependent enzyme.克氏锥虫中依赖ATP的磷酸烯醇式丙酮酸羧激酶编码基因的克隆与特性分析:与宿主依赖GTP的酶的一级结构和预测二级结构比较
Gene. 1993 Dec 22;136(1-2):69-77. doi: 10.1016/0378-1119(93)90449-d.
9
Isolation and characterization of two tightly linked catalase genes from castor bean that are differentially regulated.从蓖麻中分离并鉴定出两个紧密连锁且调控方式不同的过氧化氢酶基因。
Plant Mol Biol. 1994 Jun;25(3):507-16. doi: 10.1007/BF00043878.
10
Molecular cloning of cucumber phosphoenolpyruvate carboxykinase and developmental regulation of gene expression.黄瓜磷酸烯醇式丙酮酸羧化激酶的分子克隆及基因表达的发育调控
Plant Mol Biol. 1994 Oct;26(1):423-34. doi: 10.1007/BF00039551.

C4单子叶植物类蜀黍中的磷酸烯醇式丙酮酸羧激酶由四个差异表达的基因编码。

Phosphoenolpyruvate carboxykinase in the C(4) monocot Urochloa panicoides is encoded by four differentially expressed genes.

作者信息

Finnegan P M, Suzuki S, Ludwig M, Burnell J N

机构信息

Division of Biochemistry and Molecular Biology, Faculty of Science, Australian National University, Canberra, Australian Capital Territory 0200, Australia.

出版信息

Plant Physiol. 1999 Aug;120(4):1033-42. doi: 10.1104/pp.120.4.1033.

DOI:10.1104/pp.120.4.1033
PMID:10444086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC59336/
Abstract

Previous screening of a cDNA library of leaf poly(A(+)) RNA from Urochloa panicoides, a phosphoenolpyruvate carboxykinase (PCK)-type C(4) monocot, led to the characterization of cDNAs encoding the U. panicoides PCK subunit PCK1. A second PCK sequence, designated PCK2, has now been found by rescreening the library. The deduced PCK2 polypeptide is 626 residues in length, has a predicted molecular mass of 68,686 D, and is 96% identical to the deduced PCK1 sequence. Isolation and characterization of genomic DNA fragments revealed that the PCK1 and PCK2 genes are each closely linked to another PCK gene. These additional genes have been designated PCK3 and PCK4, respectively. In each case, the second gene is located upstream and in the same transcriptional orientation as the gene characterized through cDNA analysis. A reverse transcription-polymerase chain reaction assay was used to demonstrate that PCK1 and PCK2 transcripts predominate in leaves, whereas PCK3 and PCK4 transcripts predominate in roots. Moreover, accumulation of PCK1 and PCK2 transcripts is light dependent. Direct N-terminal sequencing of PCK polypeptides purified from leaves demonstrated that PCK2 is produced. These results strongly suggest that PCK1 and PCK2 are involved in the photosynthetic CO(2)-concentrating mechanism active in U. panicoides.

摘要

先前对黍稷(一种磷酸烯醇式丙酮酸羧激酶(PCK)型C4单子叶植物)叶片多聚腺苷酸(poly(A+))RNA的cDNA文库进行筛选,从而鉴定出了编码黍稷PCK亚基PCK1的cDNA。现在,通过对该文库进行重新筛选,发现了第二个PCK序列,命名为PCK2。推导的PCK2多肽长度为626个残基,预测分子量为68,686 D,与推导的PCK1序列有96%的同一性。基因组DNA片段的分离和鉴定表明,PCK1和PCK2基因各自与另一个PCK基因紧密连锁。这些额外的基因分别被命名为PCK3和PCK4。在每种情况下,第二个基因位于上游,并且与通过cDNA分析鉴定的基因转录方向相同。采用逆转录-聚合酶链反应分析来证明PCK1和PCK2转录本在叶片中占主导地位,而PCK3和PCK4转录本在根中占主导地位。此外,PCK1和PCK2转录本的积累依赖于光照。对从叶片中纯化的PCK多肽进行直接N端测序证明PCK2是有表达的。这些结果有力地表明,PCK1和PCK2参与了黍稷中活跃的光合CO2浓缩机制。