Tsujibo H, Kondo N, Tanaka K, Miyamoto K, Baba N, Inamori Y
Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.
J Bacteriol. 1999 Sep;181(17):5461-6. doi: 10.1128/JB.181.17.5461-5466.1999.
We purified from the culture supernatant of Alteromonas sp. strain O-7 and characterized a transglycosylating enzyme which synthesized beta-(1-->6)-(GlcNAc)2, 2-acetamido-6-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-2- deoxyglucopyranose from beta-(1-->4)-(GlcNAc)2. The gene encoding a novel transglycosylating enzyme was cloned into Escherichia coli, and its nucleotide sequence was determined. The molecular mass of the deduced amino acid sequence of the mature protein was determined to be 99,560 Da which corresponds very closely with the molecular mass of the cloned enzyme determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The molecular mass of the cloned enzyme was much larger than that of enzyme (70 kDa) purified from the supernatant of this strain. These results suggest that the native enzyme was the result of partial proteolysis occurring in the N-terminal region. The enzyme showed significant sequence homology with several bacterial beta-N-acetylhexosaminidases which belong to family 20 glycosyl hydrolases. However, this novel enzyme differs from all reported beta-N-acetylhexosaminidases in its substrate specificity. To clarify the role of the enzyme in the chitinolytic system of the strain, the effect of beta-(1-->6)-(GlcNAc)2 on the induction of chitinase was investigated. beta-(1-->6)-(GlcNAc)2 induced a level of production of chitinase similar to that induced by the medium containing chitin. On the other hand, GlcNAc, (GlcNAc)2, and (GlcNAc)3 conversely repressed the production of chitinase to below the basal level of chitinase activity produced constitutively in medium without a carbon source.
我们从交替单胞菌属菌株O - 7的培养上清液中纯化出一种转糖基酶,并对其进行了表征。该酶能从β-(1→4)-(GlcNAc)₂合成β-(1→6)-(GlcNAc)₂,即2 - 乙酰氨基 - 6 - O-(2 - 乙酰氨基 - 2 - 脱氧 - β - D - 吡喃葡萄糖基)-2 - 脱氧吡喃葡萄糖。编码这种新型转糖基酶的基因被克隆到大肠杆菌中,并测定了其核苷酸序列。推导的成熟蛋白氨基酸序列的分子量为99,560 Da,这与通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳测定的克隆酶的分子量非常接近。克隆酶的分子量比从该菌株上清液中纯化的酶(70 kDa)大得多。这些结果表明天然酶是N端区域发生部分蛋白水解的产物。该酶与属于20家族糖基水解酶的几种细菌β - N - 乙酰己糖胺酶具有显著的序列同源性。然而,这种新型酶在底物特异性方面与所有已报道的β - N - 乙酰己糖胺酶不同。为了阐明该酶在菌株几丁质分解系统中的作用,研究了β-(1→6)-(GlcNAc)₂对几丁质酶诱导的影响。β-(1→6)-(GlcNAc)₂诱导的几丁质酶产生水平与含几丁质的培养基诱导的水平相似。另一方面,GlcNAc、(GlcNAc)₂和(GlcNAc)₃则相反,将几丁质酶的产生抑制到低于在无碳源培养基中组成型产生的几丁质酶活性的基础水平。