2015
DOI: 10.1111/ijfs.12739
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Purification and characterisation of β‐mannanase from Lactobacillus plantarum (M24) and its applications in some fruit juices

Abstract: Summary β‐Mannanase was purified 2619.05‐fold from the Lactobacillus plantarum (M24) bacterium by ammonium sulphate precipitation and ion exchange chromatography (DEAE‐Sephadex). The purified enzyme gave two protein bands at a level of approximately 36.4 and 55.3 kDa in the SDS‐PAGE. The purified mannanase enzyme has shown its maximum activity at 50 °C and pH 8, and it has been also determined that the enzyme was stable at 5–11 pH range and over 50 °C. The Vmax and Km values have been identified as 82 mg manna… Show more

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Cited by 25 publications
(24 citation statements)
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“…Results were compared to values of standard graphics plotted by using bovine serum albumin, and the total protein values in the samples were calculated. The sensitivity of this method is 1 to 100 μg [14]. …”
Section: Methodsmentioning
confidence: 99%
“…Results were compared to values of standard graphics plotted by using bovine serum albumin, and the total protein values in the samples were calculated. The sensitivity of this method is 1 to 100 μg [14]. …”
Section: Methodsmentioning
confidence: 99%
“…Then, the precipitate was dissolved in 20 mM Na-acetate buffer at pH 5.5. It was then dialyzed against the same buffer [8,9,10].…”
Section: Purification Of the Phytase Enzyme From Oakbug Milkcap Mushrmentioning
confidence: 99%
“…The gels were dyed by the coomassie brilliant blue R 250 (Nadaroglu et al, 2015). The PDQuset image software (Bio-Rad Co., California, USA) was used to analyse differential protein spots.…”
Section: Two-dimensional Gel Electrophoresis (2-de)mentioning
confidence: 99%