scholarly journals Nitrogen deprivation-induced de novo transcriptomic profiling of the oleaginous green alga Botryococcus braunii 779

Genomics Data ◽  
2015 ◽  
Vol 6 ◽  
pp. 231-233 ◽  
Author(s):  
Zhenyu Xu ◽  
Jing He ◽  
Shuyuan Qi ◽  
Jianhua Liu
1986 ◽  
Vol 25 (8) ◽  
pp. 1869-1872 ◽  
Author(s):  
P. Metzger ◽  
J. Templier ◽  
C. Largeau ◽  
E. Casadevall

PLoS ONE ◽  
2021 ◽  
Vol 16 (11) ◽  
pp. e0259833
Author(s):  
Li Wei ◽  
Wuxin You ◽  
Zhengru Xu ◽  
Wenfei Zhang

Single-cell red microalga Porphyridium cruentum is potentially considered to be the bioresource for biofuel and pharmaceutical production. Nitrogen is a kind of nutrient component for photosynthetic P. cruentum. Meanwhile, nitrogen stress could induce to accumulate some substances such as lipid and phycoerythrin and affect its growth and physiology. However, how marine microalga Porphyridium cruentum respond and adapt to nitrogen starvation remains elusive. Here, acclimation of the metabolic reprogramming to changes in the nutrient environment was studied by high-throughput mRNA sequencing in the unicellular red alga P. cruentum. Firstly, to reveal transcriptional regulation, de novo transcriptome was assembled and 8,244 unigenes were annotated based on different database. Secondly, under nitrogen deprivation, 2100 unigenes displayed differential expression (1134 upregulation and 966 downregulation, respectively) and some pathways including carbon/nitrogen metabolism, photosynthesis, and lipid metabolism would be reprogrammed in P. cruentum. The result demonstrated that nitrate assimilation (with related unigenes of 8–493 fold upregulation) would be strengthen and photosynthesis (with related unigenes of 6–35 fold downregulation) be impaired under nitrogen deprivation. Importantly, compared to other green algae, red microalga P. cruentum presented a different expression pattern of lipid metabolism in response to nitrogen stress. These observations will also provide novel insight for understanding adaption mechanisms and potential targets for metabolic engineering and synthetic biology in P. cruentum.


2011 ◽  
Vol 4 (3) ◽  
pp. 229-242
Author(s):  
Zhila Natalia O. ◽  
◽  
Kalachova Galina S. ◽  
Volova Tatiana G. ◽  
◽  
...  

2021 ◽  
Vol 16 (1) ◽  
pp. 59-68
Author(s):  
Sing Tung Teng ◽  
Ing Kuo Law ◽  
Afiqah Hamilton Hanifah ◽  
Othman Bin Bojo ◽  
Farah Akmal Idrus ◽  
...  

2012 ◽  
Vol 109 ◽  
pp. 282-286 ◽  
Author(s):  
Masato Baba ◽  
Motohide Ioki ◽  
Nobuyoshi Nakajima ◽  
Yoshihiro Shiraiwa ◽  
Makoto M. Watanabe

1980 ◽  
Vol 19 (6) ◽  
pp. 1081-1085 ◽  
Author(s):  
C. Largeau ◽  
E. Casadevall ◽  
C. Berkaloff

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Weibo Ren ◽  
Xiangyang Hou ◽  
Zinian Wu ◽  
Lingqi Kong ◽  
Huiqin Guo ◽  
...  

1987 ◽  
Vol 51 (2) ◽  
pp. 493-498 ◽  
Author(s):  
Katsumi YAMAGUCHI ◽  
Hiroshi NAKANO ◽  
Masahiro MURAKAMI ◽  
Shoji KONOSU ◽  
Osamu NAKAYAMA ◽  
...  

2005 ◽  
Vol 4 (2) ◽  
pp. 253-261 ◽  
Author(s):  
Tudor Borza ◽  
Cristina E. Popescu ◽  
Robert W. Lee

ABSTRACT The presence of plastids in diverse eukaryotic lineages that have lost the capacity for photosynthesis is well documented. The metabolic functions of such organelles, however, are poorly understood except in the case of the apicoplast in the Apicomplexa, a group of intracellular parasites including Plasmodium falciparum, and the plastid of the green alga Helicosporidium sp., a parasite for which the only host-free stage identified in nature so far is represented by cysts. As a first step in the reconstruction of plastid functions in a nonphotosynthetic, predominantly free-living organism, we searched for expressed sequence tags (ESTs) that correspond to nucleus-encoded plastid-targeted polypeptides in the green alga Prototheca wickerhamii. From 3,856 ESTs, we found that 71 unique sequences (235 ESTs) correspond to different nucleus-encoded putatively plastid-targeted polypeptides. The identified proteins predict that carbohydrate, amino acid, lipid, tetrapyrrole, and isoprenoid metabolism as well as de novo purine biosynthesis and oxidoreductive processes take place in the plastid of P. wickerhamii. Mg-protoporphyrin accumulation and, therefore, plastid-to-nucleus signaling might also occur in this nonphotosynthetic organism, as we identified a transcript which encodes subunit I of Mg-chelatase, the enzyme which catalyzes the first committed step in chlorophyll synthesis. Our data indicate a far more complex metabolism in P. wickerhamii's plastid compared with the metabolic pathways predicted to be located in the apicoplast of P. falciparum and the plastid of Helicosporidium sp.


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