A. Bartesaghi et al. 2.2 Å resolution cryo - EM structure of β -
galactosidase in complex with a cell - permeant inhibitor.
The Tetrahymena intervening sequence (IVS) has been inserted into the gene for the alpha - donor fragment of beta -
galactosidase in a recombinant plasmid.
Not exact matches
Coupling of Tetrahymena ribosomal RNA splicing to beta -
galactosidase expression
in Escherichia coli
In mice heterozygous for tau - lacZ targeted to the melanopsin gene locus, β - galactosidase — positive RGC axons projected to the SCN and other brain nuclei involved in circadian photoentrainment or the pupillary light refle
In mice heterozygous for tau - lacZ targeted to the melanopsin gene locus, β -
galactosidase — positive RGC axons projected to the SCN and other brain nuclei involved
in circadian photoentrainment or the pupillary light refle
in circadian photoentrainment or the pupillary light reflex.
In the current test, these were the molecules p16, p21 and a positive test for beta -
galactosidase activity.
In one example, Subramaniam's team recently solved the structure of a relatively small protein, β -
galactosidase, to a resolution of 2.2 Å.
Brandon Hall et al (2017) p16 (Ink4a) and senescence - associated β -
galactosidase can be induced
in macrophages as part of a reversible response to physiological stimuli (http://www.aging-us.com/article/101268/text) or (https://doi.org/10.18632/aging.101268)
B. Hall et al (2016) Aging of mice is associated with p16 (Ink4a)- and β -
galactosidase - positive macrophage accumulation that can be induced
in young mice by senescent cells (http://www.aging-us.com/article/100991)
Our lead candidate, LYS - GM101, has been designed to replace this defective gene
in the cells of GM1 patients,
in order to allow for production of the functional lysosomal acid beta -
galactosidase (bgal) enzyme.
In the picture depicted, one of the two copies of the gene of the mouse was replaced with the lac Z cassette expressing the bacterial beta galactosidase and its activity in the kidney is followed by stainin
In the picture depicted, one of the two copies of the gene of the mouse was replaced with the lac Z cassette expressing the bacterial beta
galactosidase and its activity
in the kidney is followed by stainin
in the kidney is followed by staining.
In their terminally nonproliferative state both p21 + / + and p21 - / - cultures were positive for the senescence - associated beta - galactosidase (SA - beta - gal) activity; in contrast, the labeling index of p21 + / + cells was low (< 5 %) whereas the labeling index of p21 - / - cells was high (> 30 %
In their terminally nonproliferative state both p21 + / + and p21 - / - cultures were positive for the senescence - associated beta -
galactosidase (SA - beta - gal) activity;
in contrast, the labeling index of p21 + / + cells was low (< 5 %) whereas the labeling index of p21 - / - cells was high (> 30 %
in contrast, the labeling index of p21 + / + cells was low (< 5 %) whereas the labeling index of p21 - / - cells was high (> 30 %).
Selection for expression of the gene requires transcription from a cellular promoter, and consequently a mutation
in a cellular gene, and the activity of the tagged gene can be followed by staining for beta
galactosidase activity.
In vitro, Pds has been shown to produce β - glucosidase, N - acetyl - β - glucosaminidase, acid and alkaline phosphatases, esterase / esterase lipase / lipase, leucine and vailine arylamidase, naphthol - AS - B1 - phophohydrolase, various proteinases (albumin / casein / gelatin), and urease, while no enzymatic activity was indicated for cystine arylamidase, α - chymotrypsin, alpha / beta
galactosidase, trypsin, β - glucoronidase, α - fucosidase, and α - mannosidase [11].
In this approach, a promoterless reporter gene (for instance encoding beta
galactosidase, or beta geo) is introduced into ES cells.
Importantly, although cells
in prostate cancer cell holoclones were homogenously small and senescence - associated β -
galactosidase (SA - βgal) negative, most cells
in paraclones were flat and large and SA - βgal positive (Supplementary Fig.
Alpha -
galactosidase is
in the normal intestinal bacteria (
in the colon) and can break down oligosaccharides, but it is not
in the intestinal mucosa.
These carbohydrates escape digestion because there is no α -
galactosidase activity
in mammalian intestinal mucosa and because they are not absorbed into the blood.
Consequently, bacteria
in the lower intestinal tract metabolize them to form large amounts of carbon dioxide and hydrogen and to lower the pH. The amount and pattern of expelled gases reflect differences
in type, location, and abundance of intestinal microorganisms possessing α -
galactosidase activity
in a favorable nutrient environment.
Comparative effects of exogenous lactase (beta -
galactosidase) preparations on
in vivo lactose digestion.
Corazza GR, Benati G, Sorge M, et al. beta -
Galactosidase from Aspergillus niger
in adult lactose malabsorption: a double - blind crossover study.
In humans, alpha - galactosidase is normally found within lysosomes, but not expressed in the gastrointestinal tract.
In humans, alpha -
galactosidase is normally found within lysosomes, but not expressed
in the gastrointestinal tract.
in the gastrointestinal tract.??
α -
Galactosidase, found
in the product Beano, can be used to digest the galactosyl units from these oligosaccharides, leaving sucrose for further digestion.