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关于导致纺织染料 Rubine 3GP 脱色和降解的重要微生物相互作用的研究。

A study on significant microbial interaction leading to decolorization and degradation of textile dye Rubine 3GP.

机构信息

Department of Biochemistry, Shivaji University, Kolhapur, India.

出版信息

J Basic Microbiol. 2011 Oct;51(5):499-514. doi: 10.1002/jobm.201000409. Epub 2011 Mar 24.

Abstract

The present study evaluates an obligatory interaction between the yeast Saccharomyces cerevisiae NCIM 3312 and the bacterium Pseudomonas sp. strain BCH3 for the biodegradation of the dye Rubin 3GP (R3GP). No significant degradation of R3GP was observed either by Saccharomyces cerevisiae NCIM 3312 or by Pseudomonas sp. strain BCH3, when both the cultures were tested individually under their respective optimum medium conditions. However, when both of them were allowed to intermingle with each other, R3GP was found to be degraded within 72 h, with a steady increase in β -1,3-glucanase, chitinase and protease activity in the culture supernatant; indicating the possible role of Pseudomonas sp. strain BCH3 in cell wall lysis of S. cerevisiae NCIM 3312. The present study elucidates a rare microbial interaction where the bacterium Pseudomonas sp. strain BCH3 utilizes lysed yeast cells as the sole source of nutrients for its own growth and subsequently performs decolorization and degradation of R3GP. Enzymatic status showed involvement of various oxidoreductive enzymes like lignin peroxidase, laccase, DCIP reductase and azo reductase, indicating their role in decolorization and degradation of R3GP. Degradation was confirmed using HPLC, FTIR analysis and the biochemical pathway of degradation was elucidated by using GC-MS analysis.

摘要

本研究评估了酵母 Saccharomyces cerevisiae NCIM 3312 和细菌 Pseudomonas sp. strain BCH3 之间的强制性相互作用,以生物降解染料 Rubin 3GP (R3GP)。当单独在各自的最佳培养基条件下测试酿酒酵母 NCIM 3312 和假单胞菌 sp. strain BCH3 时,均未观察到 R3GP 有明显降解。然而,当两者允许相互混合时,发现 R3GP 在 72 小时内被降解,培养上清液中的 β-1,3-葡聚糖酶、几丁质酶和蛋白酶活性稳步增加;表明假单胞菌 sp. strain BCH3 可能在酿酒酵母 NCIM 3312 的细胞壁裂解中起作用。本研究阐明了一种罕见的微生物相互作用,其中细菌 Pseudomonas sp. strain BCH3 利用裂解的酵母细胞作为其自身生长的唯一营养源,随后对 R3GP 进行脱色和降解。酶学状态表明涉及各种氧化还原酶,如木质素过氧化物酶、漆酶、DCIP 还原酶和偶氮还原酶,表明它们在 R3GP 的脱色和降解中起作用。使用 HPLC、FTIR 分析进行了降解确认,并使用 GC-MS 分析阐明了降解的生化途径。

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