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杂交拉格酵母组巴氏酵母中α-乙酰乳酸产量的变化及ILV6基因核心作用的确认

Variation in α-acetolactate production within the hybrid lager yeast group Saccharomyces pastorianus and affirmation of the central role of the ILV6 gene.

作者信息

Gibson Brian, Krogerus Kristoffer, Ekberg Jukka, Monroux Adrien, Mattinen Laura, Rautio Jari, Vidgren Virve

机构信息

VTT Technical Research Centre of Finland, Espoo, Finland.

出版信息

Yeast. 2015 Jan;32(1):301-16. doi: 10.1002/yea.3026. Epub 2014 Aug 6.

Abstract

A screen of 14 S. pastorianus lager-brewing strains showed as much as a nine-fold difference in wort total diacetyl concentration at equivalent stages of fermentation of 15°Plato brewer's wort. Two strains (A153 and W34), with relatively low and high diacetyl production, respectively, but which did not otherwise differ in fermentation performance, growth or flavour production, were selected for further investigation. Transcriptional analysis of key genes involved in valine biosynthesis showed differences between the two strains that were consistent with the differences in wort diacetyl concentration. In particular, the ILV6 gene, encoding a regulatory subunit of acetohydroxy acid synthase, showed early transcription (only 6 h after inoculation) and up to five-fold greater expression in W34 compared to A153. This earlier transcription was observed for both orthologues of ILV6 in the S. pastorianus hybrid (S. cerevisiae × S. eubayanus), although the S. cerevisiae form of ILV6 in W34 also showed a consistently higher transcript level throughout fermentation relative to the same gene in A153. Overexpression of either form of ILV6 (by placing it under the control of the PGK1 promoter) resulted in an identical two-fold increase in wort total diacetyl concentration relative to a control. The results confirm the role of the Ilv6 subunit in controlling α-acetolactate/diacetyl concentration and indicate no functional divergence between the two forms of Ilv6. The greater contribution of the S. cerevisiae ILV6 to acetolactate production in natural brewing yeast hybrids appears rather to be due to higher levels of transcription relative to the S. eubayanus form.

摘要

对14株巴氏酵母拉格啤酒酿造菌株进行的筛选显示,在15°柏拉图麦芽汁发酵的同等阶段,麦芽汁总双乙酰浓度相差高达9倍。分别选择了两株双乙酰产量相对较低和较高的菌株(A153和W34),这两株菌株在发酵性能、生长或风味产生方面没有其他差异,用于进一步研究。对缬氨酸生物合成相关关键基因的转录分析表明,这两株菌株之间的差异与麦芽汁双乙酰浓度的差异一致。特别是,编码乙酰羟酸合酶调节亚基的ILV6基因在接种后仅6小时就出现早期转录,与A153相比,W34中的表达量高达5倍。在巴氏酵母杂种(酿酒酵母×真贝酵母)中,ILV6的两个直系同源基因都观察到了这种早期转录,尽管在整个发酵过程中,W34中酿酒酵母形式的ILV6相对于A153中的同一基因也始终表现出更高的转录水平。将任何一种形式的ILV6(通过置于PGK1启动子的控制之下)过表达,相对于对照,麦芽汁总双乙酰浓度均出现相同的两倍增加。结果证实了Ilv6亚基在控制α-乙酰乳酸/双乙酰浓度方面的作用,并表明两种形式的Ilv6之间没有功能差异。在天然酿造酵母杂种中,酿酒酵母ILV6对乙酰乳酸产生的更大贡献似乎是由于相对于真贝酵母形式具有更高的转录水平。

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