Alteromonas and method thereby for producing gel-type enteromorpha polysaccharide degrading enzyme by using Alteromonas
A technology of Alteromonas and Enteromorpha polysaccharide, which is applied in the field of Alteromonas, can solve the problem of difficult degradation of Enteromorpha polysaccharide
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Embodiment 1
[0046] Embodiment 1: a kind of alteromonas A321 (Alteromonas cdwelliana A321), this bacterial strain has the following characteristics: bacterial strain is the gram-negative coryneform bacillus, without capsule, without spore, has terminal flagella, and size is about 0.3-0.7 μm×1.8-2.4μm; after the strain was cultured on the gel-type Enteromorpha polysaccharide medium at 28°C for 48 hours, the colony diameter was 2-3mm, round milky yellow, smooth edge, raised in the middle, moist and easy to pick; Adding iodine solution to the final plate can produce obvious gel-type enteromorpha polysaccharide degradation transparent circle; strain A321 can hydrolyze starch, is negative for oxidase, cannot oxidize ethanol to acetic acid, and does not produce H 2 S, produces pigment, cannot utilize citrate, malonate, indole test is negative, can utilize α-glucose, cannot utilize cellobiose, sucrose, D-glucose, D-maltose, D-mannose, L- Arabinol, ancient sugar, D-tagatose, D-trehalose, D-mannito...
Embodiment 2
[0047] Embodiment 2: the growth characteristic of a kind of Alteromonas cdwelliana A321 (Alteromonas cdwelliana A321) described in embodiment 1 is: the growth temperature range of this bacterium is 10-40 ℃, and optimum growth temperature is 28 ℃; growth pH range 3-11, the optimum growth pH range is 7.
Embodiment 3
[0048] Embodiment 3: a kind of method for the production of gel type enteromorpha polysaccharide degrading enzyme by Alteromonas A321 (Alteromonas cdwellianaA321) described in any one of embodiment 1 or 2, its steps are as follows;
[0049] (1) Inoculate the bacteria stored on the gel-type Enteromorpha polysaccharide medium into the fermentation medium, rotate at 170r / min, and cultivate at 28°C for 24h to obtain the seed solution;
[0050] (2) The seed liquid is inoculated into the fermentation medium with an inoculum size of 8%, cultivated at 170r / min at 28°C for 12-18h; the fermentation liquid is centrifuged at 10000r / min for 5min, the supernatant is taken, and 60% ammonium sulfate is added, Centrifuge overnight at 4°C at 10,000 r / min, and redissolve the precipitate with an equal volume of distilled water to obtain a crude enzyme solution.
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