• 제목/요약/키워드: starvation response

검색결과 63건 처리시간 0.026초

Effect of Post-hatch Nutrient Intubation on Performance, Intestinal Growth, Meat Yield and Immune Response in Broiler Chickens

  • Bhanja, S.K.;Anjali Devi, C.;Panda, A.K.;Sunder, G.Shyam
    • Asian-Australasian Journal of Animal Sciences
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    • 제23권4호
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    • pp.515-520
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    • 2010
  • The response of broiler chicks to intubation of nutrients (starch, casein, soybean oil or their combinations) into the crop immediately after hatch was evaluated for performance, intestinal development, meat yield and immune competence up to 35 d of age. A control group with no access to feed and two test groups fed either inert material (sawdust) or starter diet for the initial 24 h after hatch were compared with nutrient intubated groups (n = 7). A total of 300 broiler chicks were equally distributed to 10 dietary groups with 6 replicates of 5 chicks each. After 24 h of hatch, all groups were fed ad libitum the starter (0-21 d) and finisher diets (22-35 d). Results indicated that post-hatch intubation of starch into the crop significantly (p${\leq}$0.05) improved body weight (at 14 and 35 d of age), readyto-cook meat yields, weights of breast muscle and small intestine segments, cell-mediated immune response, ND titers and weight of bursa compared to chicks starved or fed sawdust during the initial 24 h after hatch. However, chicks with access to feed immediately after hatch or intubation of starch, soybean oil, starch+casein, starch+soybean oil or starch+casein+soybean oil exhibited similar positive effects. Intubation of casein either alone or in combination with soybean oil was superior to the starved or sawdust fed groups, but inferior to other groups for all the parameters studied. It was concluded from the study that intubation of starch individually or in combination with casein and/or soybean oil effectively circumvented the negative effects of post-hatch starvation for 24 h. Among the nutrients intubated, carbohydrate (starch) was better utilized by the chicks than protein (casein) or fat during the initial post-hatch period.

A Role for Arabidopsis miR399f in Salt, Drought, and ABA Signaling

  • Baek, Dongwon;Chun, Hyun Jin;Kang, Songhwa;Shin, Gilok;Park, Su Jung;Hong, Hyewon;Kim, Chanmin;Kim, Doh Hoon;Lee, Sang Yeol;Kim, Min Chul;Yun, Dae-Jin
    • Molecules and Cells
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    • 제39권2호
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    • pp.111-118
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    • 2016
  • MiR399f plays a crucial role in maintaining phosphate homeostasis in Arabidopsis thaliana. Under phosphate starvation conditions, AtMYB2, which plays a role in plant salt and drought stress responses, directly regulates the expression of miR399f. In this study, we found that miR399f also participates in plant responses to abscisic acid (ABA), and to abiotic stresses including salt and drought. Salt and ABA treatment induced the expression of miR399f, as confirmed by histochemical analysis of promoter-GUS fusions. Transgenic Arabidopsis plants overexpressing miR399f (miR399f-OE) exhibited enhanced tolerance to salt stress and exogenous ABA, but hypersensitivity to drought. Our in silico analysis identified ABF3 and CSP41b as putative target genes of miR399f, and expression analysis revealed that mRNA levels of ABF3 and CSP41b decreased remarkably in miR399f-OE plants under salt stress and in response to treatment with ABA. Moreover, we showed that activation of stress-responsive gene expression in response to salt stress and ABA treatment was impaired in miR399f-OE plants. Thus, these results suggested that in addition to phosphate starvation signaling, miR399f might also modulates plant responses to salt, ABA, and drought, by regulating the expression of newly discovered target genes such as ABF3 and CSP41b.

단식(斷食), 재급식(再給食)과 인슈린주사(注射)에 따른 쥐의 간세포핵단백질(肝細胞核蛋白質)에 대한 전기영동상의 분포양상 비교 (Comparison of SDS Gel Electrophoretic Patterns of Rat Liver Nuclear Proteins in Response to Starvation, Refeeding and Insulin Injection)

  • 이효사;데이비드 엠 깁슨
    • Applied Biological Chemistry
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    • 제22권3호
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    • pp.173-180
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    • 1979
  • 쥐를 48시간 굶긴 뒤에 위에 탄수화물 농도가 높은 먹이를 주거나 streptozotocin을 이용하여 당뇨병을 가지게 만든 쥐에 인슈린 주사를 주었을 때 쥐 간계포의 핵단백질중 가장 주요한 0.14M NaCl에 녹는 핵단백질, histones 그리고 페놀에 녹는 핵단백질의 분포 변화를 조사하고자 SDS gel 전기영동법을 이용하였다. 각 핵단백질 분획을 전기영동법으로 분리시킨 단백질의 상대량을 비교하였을 때 0.14M NaCl 추출물은 현저한 변화를 나타내었으나 histones과 페놀로 추출된 핵단백질 분획들은 분리된 단백질 상대량에 큰 변화가 없었다. 48시간 굶긴 쥐와 정상적으로 먹이를 준 쥐의 0.14M MaCl 추출 핵단백질 분획을 비교하였을때 분자량이 50,000 과 180,000 daltons 사이에 있는 적어도 5개의 핵단백질의 농도가 다른 핵단백질에 비교하여 크게 감소되었다. 반면 분자량이 36,000 daltons 단백질의 농도는 48시간 굶긴 쥐에게 다시 탄수화물 농도가 높은 먹이를 주었을 때 24시간 동안에 정상적으로 먹이를 준 쥐에서 관찰한 핵단백질 분포 양상과 비슷한 결과를 얻었다. 당뇨병을 가진 쥐에게 인슈린 주사를 준 쥐와 인슈린주사를 주지 않은 당뇨병 쥐의 0.14M NaCl추출 핵단백질 분획을 비교 조사한 결과는 굶은 쥐에게 탄수화물 농도가 높은 먹이를 준 다음에 얻은 뒤의 결과와 정상적으로 유사하였다. 여기서 얻은 실험결과들은 0.14M NaCl 추출 핵단백질 중에 있는 어떤 핵단백질의 분포 변화가 이미 알려진 인슈린 신호에 따라 조정되고 cytosol에 있는 지방합성에 관하는 효소(lipogenic enzymes)들의 유도에 관련된 세포핵 활성 조절에 영향을 끼치고 있음을 시사해 준다.

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오이 떡잎에서 노쇠화 관련 유전자들의 식물 호르몬에 대한 반응 연구 (Response to Plant Hormones of Senescence-related Genes for Cucumis sativus L. in Cotyledon Development)

  • 차현정;김대재
    • 생명과학회지
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    • 제26권8호
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    • pp.895-903
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    • 2016
  • 본 연구는 발달중인 오이 떡잎에 식물호르몬을 처리하여 나타나는 노쇠화 관련 유전자들(SAG)의 유전자 발현 반응을 탐구하기 위하여 수행되었다. 따라서 선별된 오이의 노쇠화 관련 유전자들에 대하여 그들의 유전자 발현 반응을 특정하기 위하여 역전사-중합효소연쇄반응(RT-PCR)을 통하여 조사되었다. 파종 후 14일 된 오이의 떡잎을 절취한 후 100 μM IAA또는 zeatin 용액 위에 두고 빛이 있거나 없는 조건에서 4일 째 까지 처리하였다. 떡잎은 2일 간격으로 회수하여 총RNA추출과 RT-PCR의 시료로 사용하였다. RT-PCR 결과에 따르면 몇몇 오이의 SAG 전사체들은 처리기간 동안에 상당한 변화를 나타냈다. 에틸렌 반응 실험에서는 처리 1일 후 반응을 나타낸 PCK, SAG 158과 SAG 288을 제외한 대부분의 오이 SAGs는 즉각 반응을 보이지 않았으나 ICL과 SAG 281은 10일 처리 후 노란 떡잎에서 강한 반응을 나타냈다. 이러한 결과들은 몇몇 오이의 SAGs가 외부적 자극에 대하여 영양 결핍이나 노쇠화 반응을 나타냄을 의미한다. 떡잎의 발달 동안에 이와 같은 노쇠화 유도 반응은 기관의 노쇠화에서 SAGs의 대사적 역할과 기능을 이해 할 수 있는 정보를 제공한다.

Stress Responses through Heat Shock Transcription Factor in S. cerevisiae

  • Hahn, Ji-Sook;Hu, Zhanzhi;Thiele, Dennis J.;Lyer, Vishwanath R.
    • 한국미생물학회:학술대회논문집
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    • 한국미생물학회 2005년도 International Meeting of the Microbiological Society of Korea
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    • pp.105-109
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    • 2005
  • Heat Shock Transcription Factor (HSF), and the promoter heat Shock Element (HSE), are among the most highly conserved transcriptional regulatory elements in nature. HSF mediates the transcriptional response of eukaryotic cells to heat, infection and inflammation, pharmacological agents, and other stresses. While HSF is essential for cell viability in yeast, oogenesis and early development in Drosophila, extended life-span in C. elegans, and extra-embryonic development and stress resistance in mammals, little is known about its full range of biological target genes. We used whole genome analyses to identify virtually all of the direct transcriptional targets of yeast HSF, representing nearly three percent of the genomic loci. The majority of the identified loci are heat-inducibly bound by yeast HSF, and the target genes encode proteins that have a broad range of biological functions including protein folding and degradation, energy generation, protein secretion, maintenance of cell integrity, small molecule transport, cell signaling, and transcription. Approximately 30% of the HSF direct target genes are also induced by the diauxic shift, in which glucose levels begin to be depleted. We demonstrate that phosphorylation of HSF by Snf1 kinase is responsible for expression of a subset of HSF targets upon glucose starvation.

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Stringent Factor Regulates Antibiotics Production and Morphological Differentiation of Streptomyces clavuligerus

  • RYU , YONG-GU;JIN, WOOK;KIM, JIN-YOUNG;KIM, JAE-YOUNG;LEE, SANG-HEE;LEE, KYE-JOON
    • Journal of Microbiology and Biotechnology
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    • 제14권6호
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    • pp.1170-1175
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    • 2004
  • The involvement of the relA and rsh genes in the morphological and physiological differentiation of Streptomyces clavuligerus was evaluated with the relA and rsh genes mutants. The morphological differentiation of S. clavuligerus was greatly affected by the disruption of the relA gene, but not very much by the disruption of the rsh gene. The altered morphological characteristics were completely restored by the complementation of the corresponding disrupted genes. Thus, it was apparent that the mycelial morphology and clavulanic acid production were severely affected by the disruption of the relA gene. Production of clavulanic acid in the submerged batch culture and glycerol-limited chemostat showed that production was inversely related to the specific growth rate in the wild-type strain. However, the production of clavulanic acid in the ${\Delta}relA$ and ${\Delta}rsh$ null mutants was completely abolished. Therefore, it seems plausible that the stringent response of S. clavuligerus to starvation for amino acids is governed mainly by ReIA, rather than Rsh, and that the (p)ppGpp synthesized immediately after the depletion of amino acids triggers the initiation of pathways for both morphological and physiological differentiation in this species.

Nucleotide Sequence on Upstream of the cdd Locus in Bacillus subtilis

  • JONG-GUK KIM;KIM, KYE-WON;SEON-KAP HWANG;JOO-WON SUH;BANG-HO SONG;SOON-DUCK HONG
    • Journal of Microbiology and Biotechnology
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    • 제5권3호
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    • pp.125-131
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    • 1995
  • A 3, 346 bp of the cdd upstream region in Bacillus subtilis was sequenced from the pSO1 (Song BH and J Neuhard. 1989. Mol. Gen. Genet 216: 462-468) and sequence homology was searched to the known genes in Genbank and European Molecular Biology Laboratory databanks. Five complete and one truncated putative coding sequences deduced from the nucleotide sequence were found through the ORF searching by Genetyx and Macvector software, and one of them was identified as the dgk (diacylglycerol kinase) gene and another, a truncated one, as the phoH (phosphate starvation-inducible gene) gene. The B. subtilis dgk gene, having a role for response to several environmental stress signals, revealed an open reading frame of 134 amino acids with 43.1% of sequence identity to the Streptococcus mutans dgk gene. The carboxy terminal 59 residues of the truncated phoH gene showed 52.7% and 34.5% of sequence identity in amino acids with the corresponding genes of Mycobacterium leprae and Escherichia coli. The four remaining coding sequences consisting of 115, 421, 91, and 91 residues were thought to be unknown ORFs because they have no significant similarity to known genes.

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Comparative study on Hsp25 expression in Mongolian gerbil and mouse cerebellum

  • Lee, Heang-Yeon;Kim, Seong-Hwan;Lee, Jae-Bong;Shin, Chang-Ho
    • 한국동물위생학회지
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    • 제29권4호
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    • pp.469-482
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    • 2006
  • The term 'heat shock protein (Hsps)' was derived from the fact that these proteins were initially discovered to be induced by hyperthermic conditions. In response to a range of stressful stimuli, including hyperthermia, immobilization, UV radiation, amino acid analogues, arsenite, various chemicals, and drugs the mammalian brain demonstrates a rapid and intense induction of the heat shock protein. Moreover, Hsps were expressed on the various pathological conditions including trauma, focal or global ischemia, hypoxia, infarction, infections, starvation, and anoxia. Especially, Hsp25 has a protective activity, facilitated by the ability of the protein to decrease the intracellular levels of reactive oxygen species (ROS) as well as its chaperone activity, which favors the degradation of oxidized proteins. Recently, it has clearly demonstrated that Hsp25 is constitutively expressed in the adult mouse cerebellum by parasagittal bands of purkinje cells in three distinct regions, the central zone (lobule VI-VII) and nodular zone (lobule IX-X), and paraflocculus. The Mongolian gerbil has been introduced into stroke study model because of its unique brain vasculature. There are no significant connections between the basilarvertebral system and the carotid system. This anatomy feature renders the mongolian gerbil susceptible to forebrain ischemia-induced seizure. The present study is designed to examine the pattern of Hsp25 expression in the cerebellum of this animal in comparison with that in mouse.

Overexpression of S-Adenosylmethionine Synthetase in Recombinant Chlamydomonas for Enhanced Lipid Production

  • Jeong Hyeon Kim;Joon Woo Ahn;Eun-Jeong Park;Jong-il Choi
    • Journal of Microbiology and Biotechnology
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    • 제33권3호
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    • pp.310-318
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    • 2023
  • Microalgae are attracting much attention as promising, eco-friendly producers of bioenergy due to their fast growth, absorption of carbon dioxide from the atmosphere, and production capacity in wastewater and salt water. However, microalgae can only accumulate large quantities of lipid in abiotic stress, which reduces productivity by decreasing cell growth. In this study, the strategy was investigated to increase cell viability and lipid production by overexpressing S-adenosylmethionine (SAM) synthetase (SAMS) in the microalga Chlamydomonas reinhardtii. SAM is a substance that plays an important role in various intracellular biochemical reactions, such as cell proliferation and stress response, and the overexpression of SAMS could allow cells to ithstand the abiotic stress and increase productivity. Compared to wild-type C. reinhardtii, recombinant cells overexpressing SAMS grew 1.56-fold faster and produced 1.51-fold more lipids in a nitrogen-depleted medium. Furthermore, under saline-stress conditions, the survival rate and lipid accumulation were 1.56 and 2.04 times higher in the SAMS-overexpressing strain, respectively. These results suggest that the overexpression of SAMS in recombinant C. reinhardtii has high potential in the industrial-scale production of biofuels and various other high-value-added materials.

Roles of YehZ, a Putative Osmoprotectant Transporter, in Tempering Growth of Salmonella enterica serovar Typhimurium

  • Kim, Seul I;Ryu, Sangryeol;Yoon, Hyunjin
    • Journal of Microbiology and Biotechnology
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    • 제23권11호
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    • pp.1560-1568
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    • 2013
  • Salmonella, a main cause of foodborne diseases, encounters a variety of environmental stresses and overcomes the stresses by multiple resistance strategies. One of the general responses to hyperosmotic stress is to import or produce compatible solutes so that cells maintain fluid balance and protect proteins and lipids from denaturation. The ProP and ProU systems are the main transport systems for compatible solutes. The OsmU system, recently identified as a third osmoprotectant transport system, debilitates excessive growth as well by reducing production of trehalose. We studied a fourth putative osmoprotectant transport system, YehZYXW, with high sequence similarity with the OsmU system. A Salmonella strain lacking YehZ, a predicted substrate-binding protein, did not suffer from hyperosmolarity but rather grew more rapidly than the wild type regardless of glycine betaine, an osmoprotectant, suggesting that the YehZYXW system controls bacterial growth irrespective of transporting glycine betaine. However, the growth advantage of ${\Delta}yehZ$ was not attributable to an increase in OtsBA-mediated trehalose production, which is responsible for the outcompetition of the ${\Delta}osmU$ strain. Overexpressed YehZ in trans was capable of deaccelerating bacterial growth vice versa, supporting a role of YehZ in dampening growth. The expression of yehZ was increased in response to nutrient starvation, acidic pH, and the presence of glycine betaine under hyperosmotic stress. Identifying substrates for YehZ will help decipher the role of the YehZYXW system in regulating bacterial growth in response to environmental cues.