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Culture method of phaeocystis globosa

A technology of Phaeocystis sphaeroides and a cultivation method, which is applied in the field of cultivation of Phaeocystis sphaeroides, can solve problems such as difficult cultivation, and achieve the effect of wide application value

Inactive Publication Date: 2017-07-21
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] The traditional method is only suitable for cultivating algae in a sterile, small-volume environment, and it is very difficult to cultivate in a 20L large-volume sterile environment

Method used

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  • Culture method of phaeocystis globosa
  • Culture method of phaeocystis globosa
  • Culture method of phaeocystis globosa

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0044] Embodiment 1: N, the influence of P on the growth of spherical brown sac

[0045] 1) Cultivate Phaeocystis globosa in transparent glass jars with 3300 Lux light, 12h / 12h light cycle, 20°C temperature, and thorough disinfection.

[0046] 2) Table 1 provides the added amount of nutrient salt, wherein the added amount of solution 1 (N, P) of the treatment group is doubled, and the control group is added as usual. According to the method described in Table 1, nutrient salt is added to the control group and the treatment group respectively every day , wherein 10 mL of solution 1 was added to the control group, and 20 mL of solution 1 was added to the treatment group.

[0047] Table 1

[0048]

[0049] 3) Detect the fluorescence value of the algae liquid at 440 / 680nm every day, and monitor continuously for more than 1 week.

[0050] 4) if figure 1 It can be seen that the doubling of solution 1 (N, P) can make the algae continue to grow.

Embodiment 2

[0051] Embodiment 2: Effects of Fe, Cu and vitamins etc. on algae growth

[0052] 1) Cultivate Phaeocystis globosa in transparent glass jars with 3300 Lux light, 12h / 12h light cycle, 20°C temperature, and thorough disinfection. Solution 1 was added according to the amount of the treatment group shown in Table 1, solution 2 (Fe, Cu, etc.) and solution 3 (vitamins) were supplied every day in the control group, and the experimental group was only supplied on the first day of algae cultivation.

[0053] 2) Detect the fluorescence value of the algae liquid at 440 / 680nm every day, and monitor continuously for 8 days.

[0054] 3) by figure 2 It can be seen that only one supplement of Fe, Cu and vitamins can maintain the growth of Phaeocystis globosa cells.

Embodiment 3

[0055] Embodiment 3: the influence of light on the growth of algae

[0056] 1) Cultivate Phaeocystis globosa in a transparent glass tank with sufficient nutrition, temperature 20°C, thorough disinfection, and photoperiod of 12h / 12h.

[0057] 2) The algae in step 1 were placed under the light intensity of 3300Lux as the experimental group, and the remaining algae tanks were placed under the light intensity of 2200Lux as the control group.

[0058] 3) Detect the fluorescence value at 440 / 680nm of different algae tanks every day, and monitor continuously for more than 10 days.

[0059] 4) from image 3 It can be clearly seen that the algae in the control group with lower light intensity grow slowly under the same conditions.

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PUM

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Abstract

The invention discloses a culture method of phaeocystis globosa, and relates to red-tide algae. The culture method comprises the following steps: inoculating an algae solution of non-sterile phaeocystis globose cultured to a log phase into a sterile f / 2 culture medium, inoculating algae seeds into an f / 2-containing triangular flask for culturing the algae seeds; inoculating all the algae solution into the triangular flask containing sterile f / 2 culture medium for culturing to the log phase; inoculating all the algae solution into a sterilized algae culturing cylinder containing treated seawater, adding nutrient salt: 10 mL of a first solution, 5 mL of a second solution and 1 mL of a third solution; culturing under an illumination period of 12 h / 12 h and a ventilation volume of 9 L / min, monitoring a fluorescence value in the morning and the evening, wherein a fluorescence intensity of 100 corresponds to 1000 cells / mu L; after growing one day, adding 6 L of the treated seawater and an equivalent amount of nutrient salt to the algae culturing cylinder; monitoring the fluorescence value at a wavelength of 440 / 680 nm once in the morning and the evening; adding 20 mL of the first solution to the algae culturing cylinder; and monitoring the fluorescence value in the morning and the evening until growing to a cell concentration.

Description

technical field [0001] The invention relates to a red tide alga—Phaeocystis sphaeroides, in particular to a method for cultivating Phaeocystis sphaeroides stably cultivated in a 20L large-volume environment. Background technique [0002] Red tide, also known as harmful algal bloom, refers to the phenomenon that in a certain sea area, planktonic microalgae, protozoa or bacteria in the ocean multiply or gather in large numbers under suitable environmental conditions, causing water quality to deteriorate and sea water to change color. Marine ecological anomalies [1]. As a kind of global water pollution, red tide not only causes serious harm to marine environment, marine fishery and mariculture, but also brings immeasurable losses to the world economy, and threatens the survival of human beings [2]. Only after we fully understand the causes of red tides, the harm of red tides to human beings, and the impact of red tides on the world economy can we better prevent the occurrence ...

Claims

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Application Information

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IPC IPC(8): C12N1/12C12R1/89
CPCC12N1/12
Inventor 郑天凌陈瑶郑伟
Owner XIAMEN UNIV
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