首页> 外文期刊>Journal of Applied Phycology >Accumulation of glycinebetaine and its synthesis from radioactive precursors under salt-stress in the cyanobacterium Aphanothece halophytica
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Accumulation of glycinebetaine and its synthesis from radioactive precursors under salt-stress in the cyanobacterium Aphanothece halophytica

机译:盐胁迫下盐生假单胞菌在盐胁迫下甘氨酸甜菜碱的积累及其从放射性前体的合成

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Growth in salt-stressed (2.0 M NaCl) Aphanothece halophytica was initially delayed during the first two days of cultivation and eventually attained the same growth rate as the control (0.5 M NaC1) cells. Glycinebetaine accumulation increased slightly in control cells but a dramatic increase of glycinebetaine occurred in salt-stressed cells during a growth period of six days. There was no apparent increase in the synthesis of [~(14)C] glycinebetaine in the control cells, in contrast to the marked increase in its synthesis in the salt-stressed cells. Increasing NaC1 concentration in the growth medium induced both the accumulation and the synthesis of glycinebetaine. Time course experiments provided evidence that [~(14)C] choline was first oxidized to [~(14)C] betaine aldehyde which was further oxidized to [~(14)C] glycinebetaine in A. halophytica. The supporting data for such a pathway were obtained from the presence of choline and betaine aldehyde dehydrogenase activities found in the membrane and cytoplasmic fractions, respectively. The activities of these two enzymes were also enhanced upon increasing NaCl concentration in the growth medium from 0.5 M to 2.0 M. Under this condition an increase of approximately 1.5- fold was observed for choline dehydrogenase activity as compared to 2.5-fold for betaine aldehyde dehydrogenase activity, suggesting a preferable induction of the latter enzyme by salt stress. A. halophytica was able to utilize [~(14)C] ethanolamine and [~(14)C] glycine for the synthesis of [~(14)C] glycinebetaine.
机译:盐胁迫(2.0 M NaCl)盐生假单胞菌的生长最初在培养的前两天被延迟,最终达到与对照(0.5 M NaCl)细胞相同的生长速率。甘氨酸甜菜碱的积累在对照细胞中略有增加,但是在六天的生长期内,盐胁迫细胞中甘氨酸甜菜碱的含量急剧增加。对照细胞中[〜(14)C]甘氨酸甜菜碱的合成没有明显增加,与盐胁迫细胞中其合成的明显增加相反。生长培养基中NaCl浓度的增加会诱导甘氨酸甜菜碱的积累和合成。时程实验提供了证据,表明[〜(14)C]胆碱首先被氧化为[〜(14)C]甜菜碱醛,然后在盐生曲霉中进一步被氧化为[〜(14)C]甘氨酸甜菜碱。这种途径的支持数据分别来自膜和细胞质部分中存在的胆碱和甜菜碱醛脱氢酶活性。当生长培养基中的NaCl浓度从0.5 M增加到2.0 M时,这两种酶的活性也得到增强。在这种条件下,胆碱脱氢酶活性提高了约1.5倍,而甜菜碱醛脱氢酶则提高了2.5倍。活性,表明盐胁迫优选诱导后一种酶。盐生土壤杆菌能够利用[〜(14)C]乙醇胺和[〜(14)C]甘氨酸合成[〜(14)C]甘氨酸甜菜碱。

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