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近紫外线辐射对大肠杆菌中诱导型色氨酸酶形成的抑制作用。

Inhibition of the induced formation of tryptophanase in Escherichia coli by near-ultraviolet radiation.

作者信息

Swenson P A, Setlow R B

出版信息

J Bacteriol. 1970 Jun;102(3):815-9. doi: 10.1128/jb.102.3.815-819.1970.

Abstract

Induced formation of tryptophanase in Escherichia coli B/r is temporarily inhibited by near-ultraviolet (UV) irradiation. The inhibition is greater when irradiation is at 5 C than when at room temperature. Hence, the inhibition is the result of a photochemical, rather than photoenzymatic, alteration of some cellular component. The action spectrum has a peak in the region of 334 nm and is similar to that for growth delay. However, inhibition of tryptophanase formation is more sensitive to near-UV irradiation than are growth, respiration, and the induced formation of beta-galactosidase. Thus, for tryptophanase the lack of formation cannot be due to general inhibition of metabolism. Pyridoxal phosphate absorbs in the near-UV region of the spectrum and is a cofactor for tryptophanase, but this enzyme in induced cells is not inactivated by near UV-radiations. An experiment in which toluene-treated suspensions from irradiated and unirradiated cells were mixed showed that irradiation does not cause the formation of an inhibitor of tryptophanase activity. The possibility remains that the absorption of radiant energy by pyridoxal phosphate interferes with the synthesis of tryptophanase.

摘要

在大肠杆菌B/r中,色氨酸酶的诱导形成会被近紫外线(UV)照射暂时抑制。在5℃照射时的抑制作用比在室温下照射时更强。因此,这种抑制是某种细胞成分发生光化学改变而非光酶改变的结果。作用光谱在334nm区域有一个峰值,且与生长延迟的作用光谱相似。然而,色氨酸酶形成的抑制对近紫外线照射比生长、呼吸作用以及β-半乳糖苷酶的诱导形成更为敏感。因此,对于色氨酸酶来说,其无法形成并非是由于代谢的普遍抑制。磷酸吡哆醛在光谱的近紫外线区域有吸收,并且是色氨酸酶的一种辅因子,但诱导细胞中的这种酶不会被近紫外线辐射灭活。一项将经照射和未照射细胞的甲苯处理悬浮液混合的实验表明,照射不会导致色氨酸酶活性抑制剂的形成。磷酸吡哆醛对辐射能的吸收干扰色氨酸酶合成的可能性仍然存在。

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The induction of beta-galactosidase and tryptophanase in X-irradiated E. coli B and B/r.
Int J Radiat Biol Relat Stud Phys Chem Med. 1977 Dec;32(6):595-601. doi: 10.1080/09553007714551391.
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Escherichia coli tryptophanase in the enteric environment.肠道环境中的大肠杆菌色氨酸酶
J Bacteriol. 1972 Jan;109(1):74-80. doi: 10.1128/jb.109.1.74-80.1972.

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