Liang L K, Wang X K, Zhu K L, Chi Z M
Department of Biochemistry, Yantai University, Yantai, 264005, China.
Biochemistry (Mosc). 2006 Dec;71(12):1291-7. doi: 10.1134/s0006297906120017.
The isolation of high-trehalose-accumulating mutant A11 from Saccharomycopsis fibuligera sdu has been previously described. In this paper, accumulation of trehalose under various stress conditions in S. fibuligera A11 was investigated. Neither activation of trehalose-6-phosphate synthase (SfTps1) nor change in trehalose content was observed under stress exposure of S. fibuligera A11 cells. A fragment of the Sftps1 gene in this strain was also cloned by degenerate PCR using the CoDeHOP strategy and multiply-aligned Tps1 sequences. This sequence allowed us to investigate the expression of the Sftps1 gene, which was also kept constant under the various stress conditions. Altogether, these results indicate that trehalose metabolism in S. fibuligera A11 in response to stress conditions clearly differs from that of Saccharomyces cerevisiae and most other fungi. The expression of the Sftps1 gene was not responsive to different stress treatments.
先前已报道过从扣囊复膜孢酵母sdu中分离出高海藻糖积累突变体A11。本文研究了扣囊复膜孢酵母A11在各种胁迫条件下海藻糖的积累情况。在扣囊复膜孢酵母A11细胞受到胁迫时,未观察到海藻糖-6-磷酸合酶(SfTps1)的激活,也未观察到海藻糖含量的变化。还使用CoDeHOP策略通过简并PCR克隆了该菌株中Sftps1基因的一个片段,并对多个Tps1序列进行了比对。该序列使我们能够研究Sftps1基因的表达,其在各种胁迫条件下也保持恒定。总之,这些结果表明,扣囊复膜孢酵母A11中响应胁迫条件的海藻糖代谢明显不同于酿酒酵母和大多数其他真菌。Sftps1基因的表达对不同的胁迫处理没有反应。