Müller Christian, Hjort Carsten M, Hansen Kim, Nielsen Jens
Center for Process Biotechnology, BioCentrum-DTU building, 223, Søltofts Plads, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark1.
Novozymes A/S, 2880 Bagsværd, Denmark2.
Microbiology (Reading). 2002 Dec;148(Pt 12):4025-4033. doi: 10.1099/00221287-148-12-4025.
In Aspergillus oryzae, one full-length chitin synthase (chsB) and fragments of two other chitin synthases (csmA and chsC) were identified. The deduced amino acid sequence of chsB was similar (87% identity) to chsB from Aspergillus nidulans, which encodes a class III chitin synthase. The sequence obtained for csmA indicated that it had high similarity to class V chitin synthases. chsB and csmA disruption strains and a strain in which chsB transcription was controlled were constructed using the nitrite reductase (niiA) promoter. The strains were examined during hyphal growth by Northern analysis, analysis of the cell-wall composition and growth in the presence of Calcofluor white (CFW). The chsB disrupted strain and the uninduced p(niiA)-chsB strain exhibited hyperbranching, they had a lower level of conidiation than the wild-type and were sensitive to CFW at 50 mg l(-1). When chsB transcription was induced in the strain containing the p(niiA)-chsB construct, the strain displayed wild-type morphology on solid medium and at sub-maximum growth rates but the wild-type morphology was not fully restored during rapid growth in batch cultivation. The csmA disruption strain displayed morphological abnormalities, such as ballooning cells, intrahyphal hyphae and conidial scars. The growth was severely inhibited in the presence of 10 mg CFW l(-1). In none of the constructed strains did the cell-wall composition differ from the wild-type. Northern analysis indicated no change in the transcription of the chitin synthase genes csmA and chsC when chsB expression was altered, and there was no change in the transcription of chsB and chsC when csmA was disrupted.
在米曲霉中,鉴定出了一种全长几丁质合酶(chsB)以及另外两种几丁质合酶(csmA和chsC)的片段。chsB推导的氨基酸序列与构巢曲霉的chsB相似(同一性为87%),后者编码III类几丁质合酶。获得的csmA序列表明它与V类几丁质合酶具有高度相似性。利用亚硝酸还原酶(niiA)启动子构建了chsB和csmA缺失菌株以及chsB转录受调控的菌株。通过Northern分析、细胞壁组成分析以及在荧光增白剂(CFW)存在下的生长情况,对这些菌株在菌丝生长过程中进行了检测。chsB缺失菌株和未诱导的p(niiA)-chsB菌株表现出超分支现象,它们的分生孢子形成水平低于野生型,并且对50 mg l(-1)的CFW敏感。当在含有p(niiA)-chsB构建体的菌株中诱导chsB转录时,该菌株在固体培养基上以及亚最大生长速率下呈现野生型形态,但在分批培养快速生长过程中野生型形态并未完全恢复。csmA缺失菌株表现出形态异常,如细胞膨胀、菌丝内菌丝和分生孢子疤痕。在10 mg CFW l(-1)存在下生长受到严重抑制。在构建的任何菌株中,细胞壁组成与野生型均无差异。Northern分析表明,当chsB表达改变时,几丁质合酶基因csmA和chsC的转录没有变化,当csmA缺失时,chsB和chsC的转录也没有变化。