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Identification of a second trans-acting gene controlling maltose fermentation in Saccharomyces carlsbergensis.

机译:鉴定控制卡尔酵母菌中的麦芽糖发酵的第二个反式作用基因。

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Maltose fermentation in Saccharomyces spp. requires the presence of a dominant MAL locus. The MAL6 locus has been cloned and shown to encode the structural genes for maltose permease (MAL61), maltase (MAL62), and a positively acting regulatory gene (MAL63). Induction of the MAL61 and MAL62 gene products requires the presence of maltose and the MAL63 gene. Mutations within the MAL63 gene produce nonfermenting strains unable to induce the two structural gene products. Reversion of these mal63 nonfermenters to maltose fermenters nearly always leads to the constitutive expression of maltase and maltose permease, and constitutivity is always linked to MAL6. We demonstrated that for one such revertant, strain C2, constitutivity did not require the MAL63 gene, since deletion disruption of this gene did not affect the constitutive expression of the structural genes. In addition, constitutivity was trans acting. Deletion disruption of the MAL6-linked structural genes for maltase and maltose permease in this strain did not affect the constitutive expression of a second, unlinked maltase structural gene. We isolated new maltose-fermenting revertants of a nonfermenting strain which carried a deletion disruption of the MAL63 gene. All 16 revertants isolated expressed maltase constitutively. In one revertant studied in detail, strain R10, constitutive expression was demonstrated to be linked to MAL6, semidominant, trans acting, and residing outside the MAL63-MAL61-MAL62 genes. From these studies we propose the existence of a second trans-acting regulatory gene at the MAL6 locus. We call this new gene MAL64. We mapped the MAL64 gene 2.3 centimorgans to the left of MAL63. The role of the MAL64 gene product in maltose fermentation is discussed.
机译:酵母菌中的麦芽糖发酵。需要存在显性MAL基因座。已克隆MAL6基因座,并显示其编码麦芽糖通透酶(MAL61),麦芽糖酶(MAL62)和正性调节基因(MAL63)的结构基因。 MAL61和MAL62基因产物的诱导需要麦芽糖和MAL63基因的存在。 MAL63基因内的突变产生非发酵菌株,无法诱导这两个结构基因产物。这些mal63非发酵剂向麦芽糖发酵罐的转化几乎总是导致麦芽糖酶和麦芽糖通透酶的组成型表达,而组成型始终与MAL6相关。我们证明,对于一种这样的回复株C2,组成性不需要MAL63基因,因为该基因的缺失破坏不会影响结构基因的组成性表达。另外,本构性是反式的。该菌株中麦芽糖酶和麦芽糖通透酶的MAL6连接的结构基因的缺失破坏不影响第二个未连接的麦芽糖酶结构基因的组成型表达。我们分离了携带MAL63基因缺失破坏的非发酵菌株的新的麦芽糖发酵还原体。分离的所有16个回复体组成型地表达麦芽糖酶。在详细研究的一个回复株中,菌株R10的组成型表达被证明与MAL6相关,半显性,反式作用并位于MAL63-MAL61-MAL62基因的外部。从这些研究中,我们建议在MAL6位点存在第二个反式调控基因。我们称这个新基因为MAL64。我们将MAL64基因2.3厘摩映射到了MAL63的左侧。讨论了MAL64基因产物在麦芽糖发酵中的作用。

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