Tisochrysis lutea

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Tisochrysis lutea
Scientific classification Edit this classification
Domain: Eukaryota
Clade: Diaphoretickes
Phylum: Haptista
Subphylum: Haptophytina
Class: Coccolithophyceae
Order: Isochrysidales
Family: Isochrysidaceae
Genus: Tisochrysis
Species:
T. lutea
Binomial name
Tisochrysis lutea
Bendif et. al. 2013

Tisochrysis lutea is a species of Haptophyta formerly known as Isochrysis affinis galbana (Tahiti isolate) or 'T-iso'.[1]

T. lutea is one of the most widely used species in aquaculture to feed oyster and shrimp larvae. It has an interesting composition for this application because of its high content of polyunsaturated fatty acids such as docosahexaenoic acid (DHA), stearidonic acid and alpha-linolenic acid.[2] T. lutea contains betain lipids and phospholipids.[3]

Etymology[edit]

The genus name Tisochrysis comes from the first letter of Tahiti, French Polynesia, where the species is first isolated, and its previous genus Isochrysis. The species name lutea stems from its color. Lutea is the color of saffron yellow in Latin.

Applications[edit]

Feeds for aquaculture[edit]

T. lutea was isolated from Tahiti, French Polynesia, by the name Isochrysis affinis galbana (Tahiti isolate) or 'T-iso'. However, by sequence of partial nuclear small subunit (SSU), large subunit rDNA and mitochondrial cytochrome oxidase 1 genes,[1] it was discovered that T. lutea is different from Isochrysis galbana and other Isochrysis spp. isolated from temperate waters . T. lutea was chosen to be feeds for larvae animals for several reasons: First, it has a fast growth rate and a wide physico-chemical tolerance range, which makes it easier to cultivate. Also, its high unsaturated fatty acid is a great merit over other choice of feeds.

Dietary Supplement[edit]

Other than feeding larvae animals, its high omega-3 fatty acids, such as Eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are also candidates for nutraceutical product for human.

T. lutea was tested on obesity and metabolism disease model. It was provided orally to Wistar rats as a long-chain polyunsaturated fatty acid source along with high-fat diet. T. lutea lowered the liver triglyceride and total cholesterol levels and improved lipopolysaccharide serum level. Abdominal and epididymal adipose tissue weight to body weight ratios of high-fat diet Wistar rats are reduced in T. lutea supplemented group, while these ratios were similar between the HF-Tiso group and CTRL rats.[4]

Anti-inflammation[edit]

T. lutea contains fucoxanthin as well. Fucoxanthin, a carotenoid pigment synthesized in brown algae, counter-act on interleukin 6, Arg 1, NLRP3 expression and other inflammatory factor, which reduces inflammation. The methanoic extraction of T. lutea is found to perform better than fucoxanthin alone as an anti-inflammatory ingredient.[5]

Its anti-inflammatory affect is tested on animal models of dry eye syndrome. T. lutea reduced the expression of NF-κB, MAPK, and AKT in vitro in human retinal epithelial ARPE-19 cells. The tear volume was increased and the cornea damage was reduced in vivo.[6]

Biodiesel[edit]

Several research also considered T. lutea as a biodiesel producer candidate because of the abundant fat it can produce. T. lutea grown under nitrogen depletion raise heating value.[7] Its nitrogen concentrations provide specific gravity, kinematic viscosity, iodine value, and cetane number that meet the standards for Europe and the U.S.A.[7]

References[edit]

  1. ^ a b Bendif, El Mahdi; Probert, Ian; Schroeder, Declan C.; de Vargas, Colomban (December 2013). "On the description of Tisochrysis lutea gen. nov. sp. nov. and Isochrysis nuda sp. nov. in the Isochrysidales, and the transfer of Dicrateria to the Prymnesiales (Haptophyta)". Journal of Applied Phycology. 25 (6): 1763–1776. Bibcode:2013JAPco..25.1763B. doi:10.1007/s10811-013-0037-0. S2CID 7878787.
  2. ^ Renaud, S. M.; Zhou, H. C.; Parry, D. L.; Thinh, Luong-Van; Woo, K. C. (1995). "Effect of temperature on the growth, total lipid content and fatty acid composition of recently isolated tropical microalgae Isochrysis sp., Nitzschia closterium, Nitzschia paleacea, and commercial species Isochrysis sp. (clone T.ISO)". Journal of Applied Phycology. 7 (6): 595–602. Bibcode:1995JAPco...7..595R. doi:10.1007/BF00003948. S2CID 206766536.
  3. ^ Kato, Misako; Sakai, Miho; Adachi, Kyoko; Ikemoto, Hisato; Sano, Hiroshi (1996). "Distribution of betaine lipids in marine algae". Phytochemistry. 42 (5): 1341–5. Bibcode:1996PChem..42.1341K. doi:10.1016/0031-9422(96)00115-X.
  4. ^ Mayer, Claire; Richard, Léo; Côme, Martine; Ulmann, Lionel; Nazih, Hassan; Chénais, Benoît; Ouguerram, Khadija; Mimouni, Virginie (February 2021). "The Marine Microalga, Tisochrysis lutea, Protects against Metabolic Disorders Associated with Metabolic Syndrome and Obesity". Nutrients. 13 (2): 430. doi:10.3390/nu13020430. ISSN 2072-6643. PMC 7911999. PMID 33525643.
  5. ^ Bigagli, Elisabetta; D’Ambrosio, Mario; Cinci, Lorenzo; Niccolai, Alberto; Biondi, Natascia; Rodolfi, Liliana; Dos Santos Nascimiento, Luana Beatriz; Tredici, Mario R.; Luceri, Cristina (2021-06-11). "A Comparative In Vitro Evaluation of the Anti-Inflammatory Effects of a Tisochrysis lutea Extract and Fucoxanthin". Marine Drugs. 19 (6): 334. doi:10.3390/md19060334. ISSN 1660-3397. PMC 8230663. PMID 34207952.
  6. ^ Hong, Sung-Chul; Yu, Hyung Seok; Kim, Jin-Woo; Lee, Eun Ha; Pan, Cheol-Ho; Hong, Kwang Won; Kim, Jin-Chul (2022-11-15). "Protective effect of Tisochrysis lutea on dry eye syndrome via NF-κB inhibition". Scientific Reports. 12 (1): 19576. Bibcode:2022NatSR..1219576H. doi:10.1038/s41598-022-23545-7. ISSN 2045-2322. PMC 9666437. PMID 36380046.
  7. ^ a b Almutairi, Adel W. (2020-10-10). "Improvement of Chemical Composition of Tisochrysis lutea Grown Mixotrophically under Nitrogen Depletion towards Biodiesel Production". Molecules (Basel, Switzerland). 25 (20): 4609. doi:10.3390/molecules25204609. ISSN 1420-3049. PMC 7587180. PMID 33050388.