Literature DB >> 14961275

Bioluminescence of Aequorea macrodactyla, a common jellyfish species in the East China Sea.

Ning-Shao Xia1, Wen-Xin Luo, Jun Zhang, Xiao-Yan Xie, Hai-Jie Yang, Shao-Wei Li, Ming Chen, Mun-Hon Ng.   

Abstract

Studies of the bioluminescent mechanisms of jellyfish have been mainly confined to one species, Aequorea victoria. We describe the luminescent system of another species, Aequorea macrodactyla, which is commonly found in the warmer waters on the coastal region of East China Sea. The luminescent system of this species consists of a green fluorescent protein (GFP) and one or more aequorins. The GFP gene is 1042 bp. It encompasses a coding sequence of 717 bp organized as 3 exons, and it is predicted to specify a 27-kDa peptide, which shares 80% amino acid sequence identity with the GFP of A. victoria. The entire coding sequence was cloned into the pTO-T7 expression vector and expressed in Escherichia coli. Compared with GFP of A. victoria, the purified expressed protein exhibited an excitation peak at a higher wavelength of 476 nm and an emission peak at a lower wavelength of 496 nm, with a higher quantum yield of 1.0. The other photoprotein, aequorin, is encoded in a single open reading frame of 585 bp specifying a 23-kDa apoprotein. The gene was cloned in to the same expression vector and expressed in E. coli. The activity of the photoprotein was reconstituted by incubating the expressed apoprotein with coelenterazine f. In the presence of Ca(2+) the reconstituted aequorin exhibits an emission peak at 470 nm. The kinetics of regeneration and the photoactivities of the reconstituted aequorins of the 2 species of jellyfish are similar. Nevertheless, Aequorea macrodactyla is expected to appear brighter and more "blue" than Aequorea victorea because of the differences in the photoactivity of their GFPs.

Entities:  

Year:  2002        PMID: 14961275     DOI: 10.1007/s10126-001-0081-7

Source DB:  PubMed          Journal:  Mar Biotechnol (NY)        ISSN: 1436-2228            Impact factor:   3.619


  11 in total

1.  Variants of green fluorescent protein GFPxm.

Authors:  Wen-Xin Luo; Tong Cheng; Bao-Quan Guan; Shao-Wei Li; Ji Miao; Jun Zhang; Ning-Shao Xia
Journal:  Mar Biotechnol (NY)       Date:  2006-07-03       Impact factor: 3.619

Review 2.  Fluorescent proteins and their use in marine biosciences, biotechnology, and proteomics.

Authors:  Gabor Mocz
Journal:  Mar Biotechnol (NY)       Date:  2007-03-19       Impact factor: 3.619

Review 3.  Genetically encodable fluorescent biosensors for tracking signaling dynamics in living cells.

Authors:  Robert H Newman; Matthew D Fosbrink; Jin Zhang
Journal:  Chem Rev       Date:  2011-04-01       Impact factor: 60.622

Review 4.  The fluorescent protein palette: tools for cellular imaging.

Authors:  Richard N Day; Michael W Davidson
Journal:  Chem Soc Rev       Date:  2009-08-04       Impact factor: 54.564

Review 5.  Live-imaging fluorescent proteins in mouse embryos: multi-dimensional, multi-spectral perspectives.

Authors:  Sonja Nowotschin; Guy S Eakin; Anna-Katerina Hadjantonakis
Journal:  Trends Biotechnol       Date:  2009-03-30       Impact factor: 19.536

6.  Characterization of Astrocyte Morphology and Function Using a Fast and Reliable Tissue Clearing Technique.

Authors:  Surya P Aryal; Khaga R Neupane; Abdullah A Masud; Christopher I Richards
Journal:  Curr Protoc       Date:  2021-10

7.  High-efficiency genome editing via 2A-coupled co-expression of fluorescent proteins and zinc finger nucleases or CRISPR/Cas9 nickase pairs.

Authors:  Katarzyna Duda; Lindsey A Lonowski; Michael Kofoed-Nielsen; Adriana Ibarra; Catherine M Delay; Qiaohua Kang; Zhang Yang; Shondra M Pruett-Miller; Eric P Bennett; Hans H Wandall; Gregory D Davis; Steen H Hansen; Morten Frödin
Journal:  Nucleic Acids Res       Date:  2014-04-21       Impact factor: 16.971

8.  A robust pipeline for rapid production of versatile nanobody repertoires.

Authors:  Peter C Fridy; Yinyin Li; Sarah Keegan; Mary K Thompson; Ilona Nudelman; Johannes F Scheid; Marlene Oeffinger; Michel C Nussenzweig; David Fenyö; Brian T Chait; Michael P Rout
Journal:  Nat Methods       Date:  2014-11-02       Impact factor: 28.547

9.  Inhibition of BET bromodomain-dependent XIAP and FLIP expression sensitizes KRAS-mutated NSCLC to pro-apoptotic agents.

Authors:  Olaf Klingbeil; Ralf Lesche; Kathy A Gelato; Bernard Haendler; Pascale Lejeune
Journal:  Cell Death Dis       Date:  2016-09-08       Impact factor: 8.469

10.  Green Fluorescence of Cytaeis Hydroids Living in Association with Nassarius Gastropods in the Red Sea.

Authors:  Andrey A Prudkovsky; Viatcheslav N Ivanenko; Mikhail A Nikitin; Konstantin A Lukyanov; Anna Belousova; James D Reimer; Michael L Berumen
Journal:  PLoS One       Date:  2016-02-03       Impact factor: 3.240

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