نتایج جستجو برای: psba

تعداد نتایج: 719  

Journal: :Biotechnology and bioengineering 2015
Javier A Gimpel James S Hyun Nathan G Schoepp Stephen P Mayfield

Recombinant protein production in microalgae chloroplasts can provide correctly folded proteins in significant quantities and potentially inexpensive costs compared to other heterologous protein production platforms. The best results have been achieved by using the psbA promoter and 5' untranslated region (UTR) to drive the expression of heterologous genes in a psbA-deficient, non-photosyntheti...

Journal: :Journal of bacteriology 2000
C Ambrosi L Leoni L Putignani N Orsi P Visca

Pseudobactin(B10), the fluorescent siderophore produced by the rhizobacterium Pseudomonas strain B10, contains the hydroxamate ligand D-N(5)-hydroxyornithine (D-N(5)-OH-Orn). We cloned the L-Orn N(5)-oxygenase (psbA) gene from a genomic library of Pseudomonas strain B10 and demonstrated that PsbA is involved in the conversion of L-Orn to its N(5)-OH derivative. PsbA shows significant similarity...

2013
Thanate Juntadech Kittisak Yokthongwattana Sithichoke Tangphatsornruang Yun-Kiam Yap Gerd Katzenmeier Chanan Angsuthanasombat

Unicellular micro-alga Chlamydomonas reinhardtii has been recognized as a promising host for expressing recombinant proteins albeit its limited utility due to low levels of heterologous protein expression. Here, transcription of the 3.4-kb mosquito-larvicidal cry4Ba gene from Bacillus thuringiensis in transgenic C. reinhardtii chloroplasts under control of the promoter and 5'-untranslated regio...

Journal: :Plant physiology 2000
M Alfonso I Perewoska D Kirilovsky

We investigated the role of the redox state of the photosynthetic and respiratory electron transport chains on the regulation of psbA expression in Synechocystis PCC 6803. Different means to modify the redox state of the electron carriers were used: (a) dark to oxidize the whole electron transport chain; (b) a shift from dark to light to induce its reduction; (c) the chemical interruption of th...

Journal: :Plant physiology 2012
Sabine Link Kerstin Engelmann Karin Meierhoff Peter Westhoff

The related proteins D1 and D2 together build up the photosystem II reaction center. Synthesis of D1 (PsbA) is highly regulated in all photosynthetic organisms. The mechanisms and specific protein factors involved in controlled expression of the psbA gene in higher plants are highly elusive. Here, we report on the identification of a chloroplast-located protein, HCF244 (for high chlorophyll flu...

Journal: :The Journal of biological chemistry 2001
T Nakamura M Ohta M Sugiura M Sugita

Post-transcriptional RNA processing is an important step in the regulation of chloroplast gene expression, and a number of chloroplast ribonucleoproteins (cpRNPs) are likely to be involved in this process. The major tobacco cpRNPs are composed of five species: cp28, cp29A, cp29B, cp31, and cp33 and these are divided into three groups (I, II, and III). By immunoprecipitation, gel filtration, and...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
B R Morton J A Levin

The psbA gene of the chloroplast genome has a codon usage that is unusual for plant chloroplast genes. In the present study the evolutionary status of this codon usage is tested by reconstructing putative ancestral psbA sequences to determine the pattern of change in codon bias during angiosperm divergence. It is shown that the codon biases of the ancestral genes are much stronger than all exta...

Journal: :Nucleic acids research 1998
C Alexander N Faber P Klaff

RNA-binding proteins play a major role in regulating mRNA metabolism in chloroplasts. In this work we characterized two proteins, of 43 and 47 kDa, which bind to the spinach psbA mRNA 5' untranslated region (psbA encoding the D1 protein of photosystem II). The 43 kDa protein, which is present in the stroma and in membranes, co-sediments with a complex of 68S. It was purified, and the N-terminal...

بارکدگذاری DNA روشی ساده برای شناسایی گونه‌ها با استفاده از یک توالی کوتاه ژنتیکی از یک بخش استاندارد ژنوم است. این روش به منظور شناسایی هشت گیاه دارویی جمع‌آوری‌شده از استان اردبیل مورد استفاده واقع شد. استخراج DNA به روش تغییر‌یافته CTAB انجام گرفت و PCR با آغازگرهای طراحی‌شده بر‌ اساس بارکدهای کلروپلاستی rbcL، trnH-psbA، matK و بارکد هسته‌ای ITS انجام شد. سپس محصولات PCR خالص‌سازی و تعیین ت...

ژورنال: شیمی آلی و پلیمر 2015

بارکدگذاری DNA روشی ساده برای شناسایی گونه‌ها با استفاده از یک توالی کوتاه ژنتیکی از یک بخش استاندارد ژنوم است. این روش به منظور شناسایی هشت گیاه دارویی جمع‌آوری‌شده از استان اردبیل مورد استفاده واقع شد. استخراج DNA به روش تغییر‌یافته CTAB انجام گرفت و PCR با آغازگرهای طراحی‌شده بر‌ اساس بارکدهای کلروپلاستی rbcL، trnH-psbA، matK و بارکد هسته‌ای ITS انجام شد. سپس محصولات PCR خالص‌سازی و تعیین ت...

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