Jittisak Senachak

Dr. Jittisak Senachak


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2019 in Peptides
Verified
Journal Article
Closed access
KAKrittima Anekthanakul
Krittima Anekthanakul
JSJittisak Senachak
Jittisak Senachak
Apiradee HongsthongApiradee Hongsthong
Apiradee Hongsthong
TCTossaton Charoonratana
Tossaton Charoonratana
MRMarasri Ruengjitchatchawalya
Marasri Ruengjitchatchawalya

5 March 2012 in Standards in Genomic Sciences
Verified
Journal Article
Open access
SCSupapon Cheevadhanarak
Supapon Cheevadhanarak
KPKalyanee Paithoonrangsarid
Kalyanee Paithoonrangsarid
PPPeerada Prommeenate
Peerada Prommeenate
WKWarunee Kaewngam
Warunee Kaewngam
AMApiluck Musigkain
Apiluck Musigkain
MTMorakot Tanticharoen
Morakot Tanticharoen
Draft genome sequence of Arthrospira platensis C1 (PCC9438)

1 January 2009 in Proteome Science
Verified
Journal Article
Open access
PDF file
Apiradee HongsthongApiradee Hongsthong
Apiradee Hongsthong
MSMatura Sirijuntarut
Matura Sirijuntarut
RYRayakorn Yutthanasirikul
Rayakorn Yutthanasirikul
JSJittisak Senachak
Jittisak Senachak
PKPavinee Kurdrid
Pavinee Kurdrid
MTMorakot Tanticharoen
Morakot Tanticharoen
The present study examined the changes in protein expression in Spirulina platensis upon exposure to high temperature, with the changes in expression analyzed at the subcellular level. In addition, the transcriptional expression level of some differentially expressed proteins, the expression pattern clustering, and the protein-protein interaction network were analyzed. The results obtained from differential expression analysis revealed up-regulation of proteins involved in two-component response systems, DNA damage and repair systems, molecular chaperones, known stress-related proteins, and proteins involved in other biological processes, such as capsule formation and unsaturated fatty acid biosynthesis. The clustering of all differentially expressed proteins in the three cellular compartments showed: (i) the majority of the proteins in all fractions were sustained tolerance proteins, suggesting the roles of these proteins in the tolerance to high temperature stress, (ii) the level of resistance proteins in the photosynthetic membrane was 2-fold higher than the level in two other fractions, correlating with the rapid inactivation of the photosynthetic system in response to high temperature. Subcellular communication among the three cellular compartments via protein-protein interactions was clearly shown by the PPI network analysis. Furthermore, this analysis also showed a connection between temperature stress and nitrogen and ammonia assimilation.

4 December 2014 in FEMS Microbiology Letters
Verified
Journal Article
Open access
PDF file
JJJiraporn Jirakkakul
Jiraporn Jirakkakul
SCSupapon Cheevadhanarak
Supapon Cheevadhanarak
JPJuntira Punya
Juntira Punya
CCChanikul Chutrakul
Chanikul Chutrakul
JSJittisak Senachak
Jittisak Senachak
AAAlongkorn Amnuaykanjanasin
Alongkorn Amnuaykanjanasin
Iron is an essential element for life. However, the iron overload can be toxic. Here, we investigated the significant increase of tenellin and iron–tenellin complex production in ferricrocin-deficient mutants of Beauveria bassiana. Our chemical analysis indicated that the ferricrocin-deficient mutants T1, T3 and T5 nearly abolished ferricrocin production. In turn, these mutants had significant accumulation of iron–tenellin complex in their mycelia at 247–289 mg g−1 cell dry weight under iron-replete condition. Both tenellin and iron–tenellin complex were not detected in the wild-type under such condition. Mass analysis of the mutants’ crude extracts demonstrated that tenellin formed a 3:1 complex with iron in the absence of ferricrocin. The unexpected link between ferricrocin and tenellin biosynthesis in ferricrocin-deficient mutants could be a survival strategy during iron-mediated oxidative stress.

17 December 2014 in Plant and Cell Physiology
Verified
Journal Article
Closed access
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JPJaruta Panyakampol
Jaruta Panyakampol
SCSupapon Cheevadhanarak
Supapon Cheevadhanarak
SSSawannee Sutheeworapong
Sawannee Sutheeworapong
JCJeerayut Chaijaruwanich
Jeerayut Chaijaruwanich
JSJittisak Senachak
Jittisak Senachak
KPKalyanee Paithoonrangsarid
Kalyanee Paithoonrangsarid
Arthrospira (Spirulina) platensis is a well-known commercial cyanobacterium that is used as a food and in feed supplements. In this study, we examined the physiological changes and whole-genome expression in A. platensis C1 exposed to high temperature. We found that photosynthetic activity was significantly decreased after the temperature was shifted from 35°C to 42°C for 2 h. A reduction in biomass production and protein content, concomitant with the accumulation of carbohydrate content, was observed after prolonged exposure to high temperatures for 24 h. Moreover, the results of the expression profiling in response to high temperature at the designated time points (8 h) revealed two distinct phases of the responses. The first was the immediate response phase, in which the transcript levels of genes involved in different mechanisms, including genes for heat shock proteins; genes involved in signal transduction and carbon and nitrogen metabolism; and genes encoding inorganic ion transporters for magnesium, nitrite and nitrate, were either transiently induced or repressed by the high temperature. In the second phase, the long-term response phase, both the induction and repression of the expression of genes with important roles in translation and photosynthesis were observed. Taken together, the results of our physiological and transcriptional studies suggest that dynamic changes in the transcriptional profiles of these thermal-responsive genes might play a role in maintaining cell homeostasis under high temperatures, as reflected in the growth and biochemical composition, particularly the protein and carbohydrate content, of A. platensis C1.

15 July 2011 in Proteome Science
Verified
Journal Article
Open access
PDF file
PKPavinee Kurdrid
Pavinee Kurdrid
JSJittisak Senachak
Jittisak Senachak
MSMatura Sirijuntarut
Matura Sirijuntarut
RYRayakorn Yutthanasirikul
Rayakorn Yutthanasirikul
PPPhuttawadee Phuengcharoen
Phuttawadee Phuengcharoen
Apiradee HongsthongApiradee Hongsthong
Apiradee Hongsthong
The present study focused on comparative proteome analyses of low- and high-temperature stresses and potential protein-protein interaction networks, constructed by using a bioinformatics approach, in response to both stress conditions. The data revealed two important points: first, the results indicate that low-temperature stress is tightly linked with oxidative stress as well as photosynthesis; however, no specific mechanism is revealed in the case of the high-temperature stress response. Second, temperature stress was revealed to be linked with nitrogen and ammonia assimilation. Moreover, the data also highlighted the cross-talk of signaling pathways. Some of the detected signaling proteins, e.g., Hik14, Hik26 and Hik28, have potential interactions with differentially expressed proteins identified in both temperature stress conditions. Some differentially expressed proteins found in the Spirulina protein-protein interaction network were also examined for their physical interactions by a yeast two hybrid system (Y2H). The Y2H results obtained in this study suggests that the potential PPI network gives quite reliable potential interactions for Spirulina. Therefore, the bioinformatics approach employed in this study helps in the analysis of phenomena where proteome analyses of knockout mutants have not been carried out to directly examine for specificity or cross-talk of signaling components.