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Driselase Sale

(Synonyms: 崩溃酶) 目录号 : GC35900

崩溃酶具有天然混合酶活性(真菌碳水化合物酶),可用于消化植物细胞壁以促进植物材料的浸渍、原生质体形成和提取过程。

Driselase Chemical Structure

Cas No.:85186-71-6

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100mg
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实验参考方法

Protocol for enzymatic hydrolysis of green tea residue by Driselase[1]:

  1. Powdered green tea (4 g) was extracted with 500 ml of hot water, and then with 100 ml of 70% ethanol three times each.
  2. The residue was digested with Driselase (1 g), pectinase andproteases in 100 ml of a 0.1 M acetate buffer (pH 5.5) at 37℃ for 24 h.
  3. To the digest, absolute ethanol was added to 70%, and the insoluble materials were removed by filtration.

Protocol for detailed protoplast isolation from hornwort tissue[2]:

  1. Incubate the hornwort tissue in 12 mL of 0.5 M mannitol in a Petri dish on an orbital shaker at 100 rpm for 30 min. In the meantime, prepare the Driselase (0.04 g/mL) in 0.5 M mannitol solution, incubate for 30 min on a rocking shaker, centrifuge at 3500 rpm for 1 min, and filter-sterilize.
  2. Add a 4mL aliquot of the Driselase solution (end concentration 1% w/v) to the hornwort tissue, and cover the Petri dishes to prevent exposure to light during incubation on the orbital shaker for 10-12 h.
  3. The protoplasts must be handled carefully during the following steps, and pipetting should be performed slowly as the protoplasts are sensitive to mechanical damage.
  4. Used a 1mL pipette tip with the tip removed (ca. 2 mm cut off from the end) or a wide-neck glass pipette. Pipette the protoplast solution through a 70µm sieve into a 50mL Falcon tube by placing the pipette tip on the mesh rather than shooting the solution through. Wash the Petri dish twice with 3 mL of 0.5 M mannitol by tilting the Petri dish and rinsing it 3-4 times for each wash.
  5. Divide the filtrate (ca. 10 mL each, topped up with 0.5 M mannitol if needed) into two glass tubes with screw caps then centrifuge at low speed for 15 min using the lowest ramp up and down speeds (600 rpm, acceleration 3, brake 3) to avoid damaging the protoplasts.
  6. Discard the supernatant and carefully resuspend each pellet in 10 mL of 0.5 M mannitol by gently running the solution down the side of the tube. Slowly tilt the tube to a 40 angle, then gently roll the tube in the palm of your hands until all the protoplasts are resuspended and no longer form clumps.
  7. Centrifuge the tubes at 600 rpm for 15 min and discard the supernatant, then carefully resuspend each pellet in 5 mL of 0.5 M mannitol and combine the samples from both tubes into one, either using cut pipette tips or by slowly allowing the sample to flow from one tube into the other.
  8. Estimate the number of protoplasts using a hematocytometer, and then centrifuge at 600 rpm for 15 min. Discard the supernatant and resuspend the protoplasts.

Protocol for protoplasting from F. verticillioides strain 3693[3]:

  1. Culture and growth condition

(1)   F. verticillioides strain 3693 was routinely grown on complete medium (CM). For conidiation, mycelial culture was inoculated on carboxy methyl cellulose medium (CMC) and incubated at 26℃ for 2 weeks.

  1. Protoplasting media preparation

(1)   Protoplasting medium consists of cell wall degrading enzymes and osmotic stabilizer.

(2)   All the lyophilized enzyme powders except driselase were first dissolved in appropriate protoplasting media. The working stock of the driselase enzyme was prepared by dissolving the enzyme powder at 2 concentration in sterile water for 30 min using the magnetic stirrer. Then the enzyme solution is filtered through the 0.2micron filter to remove the un-dissolved residues. The 0.5 ml of filtered 2 driselase solution was taken in a test tube and to that 0.5 ml of 2 osmotic stabilizer was added so that the final 1 ml of the protoplasting medium contains 1 concentration of osmotic stabilizer and 1 concentration of driselase.

(3)   Stock solution of lysing enzyme was prepared 20x concentration in water and incubated on ice for 10 min. The required amount of the lysing enzyme was added to the required amount of osmotic stabilizer to constitute the protoplasting medium.

(4)   β-glucuronidase was added at 200 units/ml of the protoplasting medium. Different osmotic chemicals such as KCl, MgSO4, NaCl, sorbitol and sucrose were used as osmotic stabilizers in the protoplasting medium. They were prepared in different concentrations viz., 0.6 M, 0.8 M, 1.0 M, 1.2 M, 1.4 M, etc. Appropriate amount of the salts was dissolved in water to achieve the required concentration and the pH was maintained at 5.6 to 5.8 and autoclave sterilized. Each treatment was replicated three times, and the experiment was repeated three times.

  1. Protoplast preparation

(1)    One ml of conidia of F. verticillioides at 109 conidia/ml was inoculated in 100 ml of YPD medium and incubated at 28℃, 250 rpm.

(2)    For harvesting different growth stages of fungi such as germinated conidia (2-10 μm length of protruded outgrowth from the conidia), germ tube (50-100 μm length of germ tube from the conidia) and well grown mycelia (germ tube grown beyond 200 μm length with two or three branched mycelia) for protoplasting, the inoculated conidia in YPD medium was incubated for 8, 12 and 24 h post-inoculation respectively.

(3)    The germinated conidia, germ tube and mycelium were collected using miracloth and the adhering residual medium was removed by washing off with sterile water three times. The mycelium was collected and used for protoplasting or stored at 4℃ for a week.

(4)    25 mg of fungal material per ml of the protoplasting medium was taken in a test tube. The fungal material was mixed well into the protoplasting medium by gentle vortexing and incubated at 30℃ and 100 rpm for different time points. The protoplasts were counted using a hemocytometer.

This protocol only provides a guideline, and should be modified according to your specific needs.

References:

[1].  Katsuno Y, Koyama Y, et,al. Apoptosis-inducing activity of a driselase digest fraction of green tea residue. Biosci Biotechnol Biochem. 2001 Jan;65(1):198-201. doi: 10.1271/bbb.65.198. PMID: 11272830.

[2]. Neubauer A, Ruaud S, et,al.Step-by-step protocol for the isolation and transient transformation of hornwort protoplasts. Appl Plant Sci. 2022 Feb 11;10(2):e11456. doi: 10.1002/aps3.11456. PMID: 35495192; PMCID: PMC9039799.

[3].Ramamoorthy V, Govindaraj L, et,al. Combination of driselase and lysing enzyme in one molar potassium chloride is effective for the production of protoplasts from germinated conidia of Fusarium verticillioides. J Microbiol Methods. 2015 Apr;111:127-34. doi: 10.1016/j.mimet.2015.02.010. Epub 2015 Feb 24. PMID: 25724844.

产品描述

Driselase is a natural mixture of enzyme activities (fungal carbohydrates) used to digest plant cell walls to facilitate the maceration of plant materials, protoplast formation, and extraction processes. Driselase releases cell wall carbohydrates.It can also be used in the preparation of fungal protoplasts [1,2].

References:
[1]. Zhang T, Tang H, et,al. Disentangling loosening from softening: insights into primary cell wall structure. Plant J. 2019 Dec;100(6):1101-1117. doi: 10.1111/tpj.14519. Epub 2019 Sep 27. PMID: 31469935.
[2]. Kaplan DT, Davis EL. Improved nematode extraction from carrot disk culture. J Nematol. 1990 Jul;22(3):399-406. PMID: 19287736; PMCID: PMC2619058.
[3].Ramamoorthy V, Govindaraj L, et,al. Combination of driselase and lysing enzyme in one molar potassium chloride is effective for the production of protoplasts from germinated conidia of Fusarium verticillioides. J Microbiol Methods. 2015 Apr;111:127-34. doi: 10.1016/j.mimet.2015.02.010. Epub 2015 Feb 24. PMID: 25724844.

崩溃酶具有天然混合酶活性(真菌碳水化合物酶),可用于消化植物细胞壁以促进植物材料的浸渍、原生质体形成和提取过程。崩溃酶可释放细胞壁内的碳水化合物,也可以用于真菌原生质体的制备[1,2,3]。

Chemical Properties

Cas No. 85186-71-6 SDF
别名 崩溃酶
Canonical SMILES [Driselase]
分子式 分子量
溶解度 10mg/mL in 20mM sodium acetate (pH 4.5) 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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动物体内配方计算器 (澄清溶液)

第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
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Research Update

Combination of Driselase and lysing enzyme in one molar potassium chloride is effective for the production of protoplasts from germinated conidia of Fusarium verticillioides

J Microbiol Methods 2015 Apr;111:127-34.PMID:25724844DOI:10.1016/j.mimet.2015.02.010.

Various cell wall degrading enzymes and the protoplasting media were evaluated for the production of protoplast in Fusarium verticillioides. Among the various enzymes tested, Driselase at 12.5 mg/ml in 1 M KCl protoplasting medium produced the maximum number of protoplast. Next to Driselase, lysing enzyme at 10 mg/ml in 1.2 M MgSO4 protoplasting medium was found to be the second best enzyme for the production of protoplast. More interestingly, the combined use of Driselase @ 12.5 mg/ml and lysing enzyme @ 10 mg/ml in 1 M KCl exhibited the additive effect on protoplast formation. Germinated conidia of F. verticillioides are the most susceptible fungal material for protoplast production. The use of sucrose at 1.2 M in the regeneration medium supported the maximum regeneration of protoplast. From the present study, we recommend Driselase (12.5 mg/ml) and lysing enzyme (10 mg/ml) in 1 M KCl protoplasting medium and germinated conidia of F. verticillioides for the maximum production of protoplasts and 1.2 M sucrose is the best osmoticum for the regeneration of protoplasts.

In vitro determination of ruminal protein degradability of alfalfa and prairie hay via a commercial protease in the presence or absence of cellulase or Driselase

J Anim Sci 1997 Aug;75(8):2215-22.PMID:9263071DOI:10.2527/1997.7582215x.

Ruminal protein degradation of alfalfa (2.62% N, 49.6% NDF, and in vivo undegradable intake protein [UIP] = 16.4% of CP) and prairie hay (.88% N, 69.4% NDF, and in vivo UIP = 44.5% of CP) was estimated using the Streptomyces griseus protease (SGP) in vitro method with or without pretreatment with two carbohydrases: cellulase from Penicillium funiculosum or Driselase from Basidiomycetes. Driselase is a broad-spectrum carbohydrase. Incubating forage samples for 48 h with cellulase or Driselase at a concentration of 800 mg/g per g of hay nearly maximized ADF and NDF disappearances. This concentration and incubation time then were used to pretreat hay samples. A 2-h pretreatment was included to evaluate the potential for reducing the analysis time. Other sets of samples were or were not pretreated with acetate buffer alone. Following pretreatment, samples were subjected to SGP for .25, .5, 1, 2, 4, 8, 12, 24, and 48 h. Pretreatment altered the sizes of protein pools and their degradation rates. When the UIP contents of the forages were estimated using SGP and a single-pool, first-order, kinetic model, cellulase (48 h) or Driselase pretreatments yielded UIP predictions that were more similar to in vivo values. Some carbohydrase and protease combinations also yielded single time-point estimates of UIP that were similar to in vivo values. Similarly, when sufficient time was permitted for protease incubation, single time-point estimates derived from protease alone were similar to in vivo values.

Sequencing of xyloglucan oligosaccharides by partial Driselase digestion: the preparation and quantitative and qualitative analysis of two new tetrasaccharides

Carbohydr Res 1994 Oct 17;263(2):285-93.PMID:7805055DOI:10.1016/0008-6215(94)00170-7.

The pentasaccharide (XXG), [formula: see text] obtained from Rosa xyloglucan, was converted to two isomeric tetrasaccharides, a and b (Xyl1.Glc3), by mild acid hydrolysis. During hydrolysis in 2 M trifluoroacetic acid at 90 degrees C, optimal yields of a and b were obtained after 20-40 min. Each tetrasaccharide was purified by preparative paper chromatography and high-pressure liquid chromatography (HPLC). The two isomers were distinguished by the products of their partial digestion with Driselase, which hydrolyses the glucosidic bonds sequentially from the non-reducing terminus: a and b yielded cellobiose and Xyl-->Glc-->Glc, respectively showing that they were [formula: see text] and [formula: see text] respectively. Tetrasaccharide b was chromatographically identical, upon HPLC on Dionex CarboPac PA1, with the tetrasaccharide produced from XXG by the action of Tropaeolum alpha-D-xylosidase, supporting the proposed structure. Xyloglucan oligosaccharides were assayed quantitatively by measurement of the yield of isoprimeverose (Xyl-->Glc) after complete Driselase digestion.

Apoptosis-inducing activity of a Driselase digest fraction of green tea residue

Biosci Biotechnol Biochem 2001 Jan;65(1):198-201.PMID:11272830DOI:10.1271/bbb.65.198.

We enzymatically digested green tea residue with Driselase, a crude preparation containing cellulase, pectinase and proteases, in order to examine the potential usefulness of the residue. A fraction of the digest soluble in 70% ethanol was found to induce the death of U937 human histiocytic lymphoma cells by apoptosis. Other enzyme preparations gave similar products with cell death-inducing activity of varing potency. The green tea residue may therefore be a useful source of potential agents with anti-cancer activity.

Step-by-step protocol for the isolation and transient transformation of hornwort protoplasts

Appl Plant Sci 2022 Feb 11;10(2):e11456.PMID:35495192DOI:10.1002/aps3.11456.

Premise: A detailed protocol for the protoplast transformation of hornwort tissue is not yet available, limiting molecular biological investigations of these plants and comparative analyses with other bryophytes, which display a gametophyte-dominant life cycle and are critical to understanding the evolution of key land plant traits. Methods and results: We describe a detailed protocol to isolate and transiently transform protoplasts of the model hornwort Anthoceros agrestis. The digestion of liquid cultures with Driselase yields a high number of viable protoplasts suitable for polyethylene glycol (PEG)-mediated transformation. We also report early signs of protoplast regeneration, such as chloroplast division and cell wall reconstitution. Conclusions: This protocol represents a straightforward method for isolating and transforming A. agrestis protoplasts that is less laborious than previously described approaches. In combination with the recently developed stable genome transformation technique, this work further expands the prospects of functional studies in this model hornwort.