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Preliminary characterisation of an Escherichia coli K5 lyase-deficient strain producing the K5 polysaccharide

机译:产生K5多糖的大肠杆菌K5裂解酶缺陷菌株的初步鉴定

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Escherichia coli K5 polysaccharide has structural analogies with N-acetylheparosan, a non-sulphated precursor of heparin and, for this reason, can be considered an attractive precursor for the production of semi-synthesis heparin analogues. This polysaccharide has two components: a high molecular weight (HMW) one and a low molecular weight (LMW) one, whose ratio varies depending on the action of a lyase enzyme synthesized by the same K5 producer strain. The present paper reports the production of the K5 polysaccharide by a spontaneous E. coli mutant strain lacking the lyase activity. Similar K5 polysaccharide yields, 180 mg l(-1) after 16 h fermentation, were obtained by both the wild and mutant strains, though K5 lyase activity was only observed in the culture filtrates from the wild strain. The time course of the specific filtrate volume (l m(-2)) and of the specific filtrate flux rate (l m(-2) h(-1)) during ultrafiltration (UF) of culture filtrates where the lyase enzyme acted on the K5 chain, showed a decrease of UF performance, probably because of membrane fouling by the LMW K5 fraction. In particular, the specific filtrate volume and specific filtrate flux rate of wild strain samples reached respectively 13 l m(-2) and 4 l m(-2) h(-1), compared to 25 l m(-2) and 15 l m(-2) h(-1) obtained from the mutant strain samples. PCR molecular analysis of the DNA region encoding for the lyase enzyme showed that, in the mutant strain, molecular rearrangements occurred in both regulatory and structural regions.
机译:大肠杆菌K5多糖具有与N-乙酰肝素聚糖(肝素的非硫酸化前体)的结构类似物,因此,可以将其视为生产半合成肝素类似物的有吸引力的前体。该多糖具有两个成分:高分子量(HMW)成分和低分子量(LMW)成分,其比例根据同一K5生产菌株合成的裂解酶的作用而变化。本论文报道了缺乏裂解酶活性的自发大肠杆菌突变菌株生产K5多糖的过程。尽管仅在野生菌株的培养滤液中观察到K5裂解酶的活性,但野生菌株和突变菌株均获得了相似的K5多糖产量,发酵16 h后达到180 mg l(-1)。特定的滤液体积(lm(-2))和特定的滤液通量率(lm(-2)h(-1))在培养物滤液超滤(UF)期间的裂解过程,裂解酶作用于K5链显示超滤性能下降,可能是由于LMW K5馏分对膜的污染。特别是,野生菌株样品的比滤液体积和比滤液通量率分别达到13 lm(-2)和4 lm(-2)h(-1),而25 lm(-2)和15 lm(- 2)从突变菌株样品中获得h(-1)。对裂解酶编码的DNA区域的PCR分子分析表明,在突变菌株中,在调控区和结构区均发生了分子重排。

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