brachymystax lenok
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2021 ◽  
Author(s):  
Yan Chen ◽  
Yang Liu ◽  
Yucen Bai ◽  
Shaogang Xu ◽  
Xiaofei Yang ◽  
...  

Abstract Changes in the metabolic profile within the intestine of lenok (Brachymystax lenok) when challenged to acute and lethal heat stress (HS) are studied using no-target HPLC-MS/MS metabonomic analysis. Of 51 differentially expressed metabolites identified in response to HS, 34 occurred in the positive ion mode and 17 in negative ion mode (VIP > 1, P < 0.05). Changes in metabolites (i.e. alpha-D-glucose, stachyose and L-lactate) related to carbohydrate and glycolysis are identified in HS-treated lenok. Fatty acid β-oxidation in HS-treated lenok was inhibited by accumulation of acetyl carnitine, palmitoylcarnitine, carnitine, and erucic acid. Many amino acids (L-tryptophan, D-proline, L-leucine, L-phenylalanine, L-aspartate, L-tyrosine, L-methionine, L-histidine and L-glutamine) decreased to support energy demands in HS-treated lenok. Oxidative damage in HS-treated lenok was indicated by decreased glycerophospholipid metabolites (i.e. glycerophosphocholine, 1-palmitoyl-2-hydroxy-sn-glycero-3-phosphoethanolamine, 1-palmitoyl-sn-glycero-3-phosphocholine, 1-stearoyl-2-oleoyl-sn-glycero-3-phosphocholine, and 1, 2-dioleoyl-sn-glycero-3-phosphatidylcholine), and increased oxylipin production (12-HETE and 9R, 10S-EpOME). Oxidative stress increased formation of eicosanoids and dicarboxylic acids, overwhelming the mitochondrial β-oxidation pathway, while minor oxidative pathways (omega-oxidation and peroxisomal beta-oxidation) were likely to be activated in HS-treated lenok.


Author(s):  
Wenbo Zhu ◽  
Zhongkai Wang ◽  
Haorong Li ◽  
Hui Xiang ◽  
Ping Li ◽  
...  

The salmonid-specific fourth vertebrate whole-genome duplication (Ss4R) occurred ~80 million years ago in the ancestor of all salmonids and provides a unique opportunity to study the evolutionary history of the duplicated genome. Study of the genome of Brachymystax lenok tsinlingensis might be particularly insightful given that this is the only Brachymystax species with a published salmonid genome. Here, we present a high-quality chromosome-level genome assembly for B. l. tsinlingensis and found that the salmonids have a unique GC content and codon usage, have undergone a whole-genome duplication event and a burst of transposon-mediated repeat expansion, have a slower evolutionary rate, and possess specific expanded gene families and unique positively selected genes. Generally, the B. l. tsinlingensis genome could provide a valuable reference for the study of other salmonids as well as aid the conservation of this endangered species.


Author(s):  
S. Assylbekova ◽  
N. Badryzlova ◽  
L. Kushnikova

The article presents the results of the first research on artificial reproduction in industrial conditions of the endemic, narrow-areal subspecies of Brachymystax lenok Savinovi, which lives in lake Markakol, East Kazakhstan region. The indicators of the heat sum characteristic for each stage of development, the rate of development and growth of the Markakolsky lenok from the moment of pre-breeding to late juveniles are described. To develop technological approaches for artificial fish reproduction, one of the most important points is to determine the optimal conditions for each stage and assess the risks (loss of fish products). At the stage of insemination and transportation of eggs to the place of incubation, the loss was 50 %. The largest losses of fish products were registered during the incubation stage. The most painlessly passed the period of holding and lifting on the float, where the loss was only 3 %. When growing pre-larvae and larvae in the pool, the daily waste did not exceed 1 %. Small-sized animals that were unable to adapt to artificial feeds fell into the waste. Losses during this period amounted to 15 % of the previous stage. In General, the yield of juveniles from the moment of fertilization to the end of the experiment was 16 %. The crucial factor in the development and growth of Lenok Markakolosky is the temperature regime. For the period of embryonic development, the most favorable water temperature is 7–8 °C. From the moment of hatching, the water temperature must be increased to 10–12 °C, and the optimal temperature for the cage growing of fingerlings varies from 12 to 14 °C.


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