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首页> 外文期刊>Applied and Environmental Microbiology >Growth of Hyperthermophilic Archaeon Pyrococcus furiosus on Chitin Involves Two Family 18 Chitinases
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Growth of Hyperthermophilic Archaeon Pyrococcus furiosus on Chitin Involves Two Family 18 Chitinases

机译:甲壳质上嗜热古细菌火球菌的生长涉及两个家族18几丁质酶。

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Pyrococcus furiosus was found to grow on chitin, adding this polysacharide to the inventory of carbohydrates utilized by this hyperthermophilic archaeon. Accordingly, two open reading frames (chiA [Pf1234] and chiB [Pf1233]) were identified in the genome of P. furiosus, which encodes chitinases with sequence similarity to proteins from the glycosyl hydrolase family 18 in less-thermophilic organisms. Both enzymes contain multiple domains that consist of at least one binding domain and one catalytic domain. ChiA (ca. 39 kDa) contains a putative signal peptide, as well as a binding domain (ChiABD), that is related to binding domains associated with several previously studied bacterial chitinases. chiB, separated by 37 nucleotides from chiA and in the same orientation, encodes a polypeptide with two different proline-threonine-rich linker regions (6 and 3 kDa) flanking a chitin-binding domain (ChiBBD [11 kDa]), followed by a catalytic domain (ChiBcat [35 kDa]). No apparent signal peptide is encoded within chiB. The two chitinases share little sequence homology to each other, except in the catalytic region, where both have the catalytic glutamic acid residue that is conserved in all family 18 bacterial chitinases. The genes encoding ChiA, without its signal peptide, and ChiB were cloned and expressed in Escherichia coli. ChiA exhibited no detectable activity toward chitooligomers smaller than chitotetraose, indicating that the enzyme is an endochitinase. Kinetic studies showed that ChiB followed Michaelis-Menten kinetics toward chitotriose, although substrate inhibition was observed for larger chitooligomers. Hydrolysis patterns on chitooligosaccharides indicated that ChiB is a chitobiosidase, processively cleaving off chitobiose from the nonreducing end of chitin or other chitooligomers. Synergistic activity was noted for the two chitinases on colloidal chitin, indicating that these two enzymes work together to recruit chitin-based substrates for P. furiosus growth. This was supported by the observed growth on chitin as the sole carbohydrate source in sulfur-free media.
机译:发现激烈热球菌在甲壳质上生长,将这种多糖添加到该超嗜热古菌利用的碳水化合物清单中。因此,在狂热假单胞菌的基因组中鉴定出两个开放阅读框(chiA [Pf1234]和chiB [Pf1233]),其编码与低嗜热性生物中的糖基水解酶家族18的蛋白质具有序列相似性的几丁质酶。两种酶均包含由至少一个结合域和一个催化域组成的多个域。 ChiA(约39 kDa)包含一个推定的信号肽,以及一个结合结构域(ChiABD),该结构域与与几种先前研究的细菌几丁质酶相关的结合结构域有关。与chiA隔开37个核苷酸且方向相同的chiB编码的多肽,具有两个不同的富含脯氨酸-苏氨酸的接头区域(6和3 kDa),两侧是几丁质结合结构域(ChiBBD [11 kDa]),然后是催化结构域(ChiBcat [35 kDa])。 chiB中没有编码明显的信号肽。这两个几丁质酶彼此之间几乎没有序列同源性,除了在催化区域外,在这两个区域都具有在所有18种细菌几丁质酶中都保守的谷氨酸催化残基。克隆编码ChiA(不包含信号肽)和ChiB的基因,并在大肠杆菌中表达。 ChiA对小于壳四糖的壳寡糖没有表现出可检测的活性,表明该酶是内切几丁质酶。动力学研究表明,ChiB遵循Michaelis-Menten对壳三糖的动力学,尽管对于较大的壳寡聚物观察到了底物抑制作用。壳寡糖上的水解模式表明,ChiB是一种壳生物苷酶,可从几丁质或其他壳寡聚体的非还原端逐步裂解壳二糖。注意到胶体几丁质上的两种几丁质酶具有协同活性,这表明这两种酶共同作用以募集基于几丁质的底物用于P. furiosus生长。在无硫培养基中观察到的几丁质作为唯一的碳水化合物来源的生长证明了这一点。

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