Immobilization and growth of clonal tissue fragments from the macrophytic red alga Gracilaria vermiculophylla on porous mesh panels

Author(s):  
Joseph A. Kraai ◽  
Gregory L. Rorrer
2016 ◽  
Vol 24 (7) ◽  
pp. 781-790 ◽  
Author(s):  
Ruoyu Liu ◽  
◽  
Zhongmin Sun ◽  
Jianting Yao ◽  
Zimin Hu ◽  
...  

2019 ◽  
Author(s):  
Muhammad Ikbal Illijas ◽  
Andriani Nasir ◽  
Dahlia Dahlia ◽  
Nur Rahmawaty Arma ◽  
Yutaka Itabashi

The red seaweed G. vermiculophylla is rich in polyunsaturated fatty acids with 20 carbon atoms, mainly arachidonic acid (AA) and eicosapentaenoic acid, which are precursors of prostaglandins (PGs). The present study aimed to elucidate the capability of the seaweed in releasing PGs using acetone powder as the crude enzyme. Crude enzyme was prepared using cold acetone. The crude enzyme was incubated with AA at different concentrations (0.1– 4 mg). For determination of PG contents, 5 µL of sample as the test solution corresponding to 0.2 g wet mass of the seaweed was injected into the HPLC. For mass spectrometer analysis, an HPLC system connected with mass spectrometer was used. Results of the study showed that t he released PGs from incubation of acetone powder and AA analyzed by HPLC consisted of PGE 2 , 15-keto-PGE 2 , 15-hydroperoxy-PGE 2 , PGA 2 , and AA while PGs detected by LC-MS were PGF 2α , PGE 2 , 15-keto-PGE 2 , 15-hydroperoxy-PGE 2 , and PGA 2 . The capability of the red algae in producing PGs was affected by available oxygen, aspirin, a cyclooxygenase inhibitor, and AA concentration. The crude enzyme of the red alga (250 mg) was capable to produce 1.63 µg and 1.32 µg of PG 2 and 15-keto-PGE 2 from incubation with 0.25 mg of AA. This method could be the one way to provide PGs in vitro to fulfill demands of PGs in the pharmaceutical industry.


PLoS ONE ◽  
2011 ◽  
Vol 6 (12) ◽  
pp. e29359 ◽  
Author(s):  
Göran M. Nylund ◽  
Florian Weinberger ◽  
Martin Rempt ◽  
Georg Pohnert

2012 ◽  
Vol 8 ◽  
pp. 283-289 ◽  
Author(s):  
Martin Rempt ◽  
Florian Weinberger ◽  
Katharina Grosser ◽  
Georg Pohnert

Chemical defense of the invasive red alga Gracilaria vermiculophylla has been studied and compared to that of the noninvasive but related Gracilaria chilensis. Both species rely on a wound-activated chemical defense that makes them less attractive to the herbivorous sea snail Echinolittorina peruviana. The chemical stress response of both species was monitored by LC–ESIMS-based metabolic profiling and revealed commonalities and differences. Both algae rely on a rapid lipoxygenase mediated transformation of arachidonic acid to known and novel oxylipins. Common products are 7,8-dihydroxyeicosatetraenoic acid and a novel eicosanoid with an unusual γ-lactone moiety. Several prostaglandins were predominantly formed by the invasive species. The role of some of these metabolites was investigated by surveying the attachment of E. peruviana on artificial food containing the respective oxylipins. Both algae species are defended against this general herbivore by 7,8-dihydroxyeicosatetraenoic acid, whereas the prostaglandins and the novel oxylipins were inactive at naturally occurring concentrations. The role of different oxylipins in the invasive potential of Gracilaria spp. is discussed.


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