Chitosan composition and method of manufacturing the same

Description

CLAIM OF PRIORITY

This application is a continuation application of application Ser. No. 18/592,551, entitled “A method for producing a complex composition of turkey tail mushroom extract-chitosan”, filed on Mar. 1, 2024. The patent application identified above is incorporated here by reference in its entirety to provide continuity of disclosure.

FIELD OF THE INVENTION

The present invention relates to a chitosan composition and method of manufacturing the same.

BACKGROUND ART

Chitin is a natural high molecular weight polymer widely found in nature. It is the main component of insect and crustacean cuticle, and is also part of the cell walls of some fungi and other organisms. Chitin is generally extracted from its natural sources by treatments with strong acid (to remove calcium deposits where required) and strong alkali (to remove proteinaceous residue). Chitin is insoluble under typical aqueous conditions and is considered to be a relatively intractable polymer (difficult to process). Dissolution of chitin to enable direct processing into fibers or other forms requires the use of unattractive solvent systems that are generally corrosive and toxic.

Fisheries is one of Vietnam's key economic sectors, bringing a large source of foreign exchange revenue to the country. In 2022, seafood export turnover will reach 11 billion USD, of which shrimp is the object with the highest export value reaching 4.1-4.2 billion USD. Currently, the intensive shrimp farming model is deployed and brings high economic efficiency in many localities across the country. Good control of environmental conditions in this farming model helps reduce the risk of disease for shrimp. However, due to the high density of shrimp, a large amount of waste during the farming process including leftover food, feces, suspended matter, molting shells of shrimp . . . has the potential to pollute the water environment, causing outbreaks, shrimp disease. In particular, a large amount of molting shells of shrimp can be obtained by siphoning every day. Taking advantage of this source of molted shells as a raw material to produce chitin and chitosan not only adds value to farmed shrimp, but also reduces pollution of the farming environment, improving value for the shrimp farming, processing and export chain, contributing to sustainable development of the fisheries industry.

In addition, refer to Table 1, survey results on the differences in physical, chemical and biological characteristics between molting shell of shrimp and shrimp shells wasted from seafood processing. This is also one of the reasons for choosing molting shell of shrimp as a potential raw material source that can be researched to be used as raw materials for chitin and chitosan production, aims to solve the current problem of shortage of raw materials to produce chitin and chitosan.

TABLE 1
Compare features physical, chemical and biological characteristics
between molting shell of shrimp and shrimp shells wasted from seafood processing

		Shrimp shells wasted
Characteristics	Molting shell of shrimp	from seafood processing
Physical	Soft and thin	Hard and thick
Chemical	High mineral content due to the process	Chitin is strongly bound to
	of mineral accumulation in the shell	proteins and minerals,
	before molting and in an amorphous	contains astaxanthin, high
	state with alternating layers of chitin,	protein content in the
	chitin-binding proteins in the cuticle are	epidermis, especially
	also calcified (including in the head and	highly concentrated in the
	body shells), contains little protein and	composition of shrimp
	astaxanthin	heads (meat and organs)
Biological	Contains chitinase enzyme	Contains chitinase enzyme,
		but quickly goes rancid due
		to its high protein content

In recent years, the industrialized production of edible mushroom such as Pleurotus pulmonarius, Pleurotus cf. floridanus, Pleurotus ostreatus, and Pleurotus citrinopileatus is rapidly developed, and the production of chitin by using non-traditional resources such as mushroom is gradually increased. Besides, the waste edible mushroom accounts for about 20% of the total yield of the edible mushroom, and provides the possibility for extracting chitin from the waste edible mushroom. Biological fermentation technology is an emerging technology and is widely applied to extraction of mushroom chitosan. However, the liquid fermentation of the fungus mycelium is directly carried out to extract chitosan from the fungus mycelium, and the problems of high equipment requirement, strict control of culture medium and culture conditions, high input cost, low product purity and the like exist.

The antibacterial activity test also showed that the bacteriostatic effect gradually increased with the decrease of the relative molecular mass of the water-soluble chitosan, especially when the relative molecular mass was about 1500. Comparative experiments have also shown that the presence of free amino groups is the basis for the antibacterial action of water-soluble chitosan. Because the positive charge of the water-soluble chitosan and its polymeric molecular structure can adsorb and aggregate with the flagella and the membrane on the surface of the pathogen, thereby inhibiting the proliferation of pathogenic bacteria.

The preparation methods of water-soluble chitosan mainly include chemical degradation method, physical degradation method and enzymatic degradation method. The chemical degradation method is divided into acid hydrolysis method and oxidation method. The acid hydrolysis method is the earliest chitosan degradation method. As early as the 1950s, detailed research was carried out. Plus, other processes such as acetic acid method, concentrated sulfuric acid method and hydrofluoric acid method appeared. However, these methods all have environmental pollution, and the reaction end point should not be controlled. Hydrogen peroxide oxidation is representative, mainly H₂O₂, H₂O₂-HCL, ClO₂ method, etc., and the disadvantage is that it is easy to produce by-products.

Enzymatic hydrolysis is the use of specific chitosanase and other non-specific enzymes, such as chitinase, cellulase, lipase and other chitosan degradation, can be used for enzymatic hydrolysis of various enzymes More than 30 kinds. Enzymatic degradation is generally superior to chemical degradation. It is carried out under milder reaction conditions. Compared to the other two methods, the enzymatic degradation method does not require the addition of a large amount of reagents and is less polluting to the environment. The specific enzyme mainly specifically cleaves the β-1,4-glycosidic bond of chitosan to achieve the purpose of degradation. No other reagents are added during the whole degradation process, no other reaction by-products are formed, which is chitosan degradation. The most ideal method, but currently the specific chitosan degrading enzyme has less source, low activity and high preparation cost. Non-specific enzymatic hydrolysis has been studied by many people, such as Jiangnan University using wheat germ lipase for degradation. Water-soluble chitosan with a homopolymeric molecular weight of tens of thousands. In addition, cellulase, papain, and glucanase are used to degrade chitosan, but the degradation efficiency is not high, and lower molecular weight cannot be obtained. Water-soluble chitosan, such as cellulase degradation by cellulase, requires about 10% of the substrate. When degraded with protease, only 40% of chitosan can be converted. Production using non-specific enzymes alone is not competitive in terms of product cost.

The physical method is mainly ultrasonic, microwave, electromagnetic wave radiation degradation method, among which the research on ultrasonic degradation method is more, and the degradation of chitosan is caused by the breakage of chemical bonds in the molecule during the radiation process. However, the degradation of water-soluble chitosan by physical degradation is limited by the degradation mechanism. The polymerization chain of chitosan is broken at random during the degradation process. The average molecular weight distribution of the product is too wide, and it is difficult to obtain a product with a molecular weight below 40,000. The low content of water-soluble chitosan of 6-8 leads to a large waste of raw materials, which greatly limits the application of physical methods.

Therefore, it is necessary to have a method of manufacturing the chitosan composition combined with chemical treatment and biological enzymatic treatment for taking its essence, to its shortcomings.

Furthermore, what is needed to have a method of manufacturing the chitosan composition using combined raw materials including the molting shell of shrimp, and oyster mushrooms.

Finally, what is needed to provide a method of manufacturing the chitosan composition is capable of dissolving in water, a pH of 7-8.5, which is economical in production and relatively controllable in product quality.

This invention provides solutions to achieve the above goals.

SUMMARY OF THE INVENTION

Accordingly, an objective of the present invention is to provide a method of manufacturing a chitosan composition comprising steps performed in the following specific order:

• • (i) preparing materials including: a microorganism solution, a fruit vinegar, an enzyme solution, and a rice alcohol has alcohol range 30%-50%;
  • (ii) creating a chitin ingredient from shrimp shells;
  • (iii) creating a chitin ingredient from oyster mushroom;
  • (iv) creating a chitin mixture by homogenously mixing (1-10) parts of the chitin ingredient from shrimp shells at step (ii) with 1 part of the chitin ingredient from oyster mushroom at step (iii);
  • (v) loading the chitin mixture into the centrifugal spray drying device having predetermined specifications to create the chitosan composition; in which predetermined specifications include: a rotate speed of 1200 rpm for 3-5 hours at temperature 20° C.-28° C.; and
  • (vi) packaging and preservation.

Another objective of the present invention is to provide the chitin ingredient from shrimp shells comprising performing in a specific order from (a) to (c):

• • (a) collecting a molting shell of shrimp, then washing to remove impurities, and soaking with HCl solution in a ratio of 1: (3-5) (w/v) for 15-20 days, then filtering to remove liquid, washing twice with the rice alcohol has alcohol range 30%-50% to obtain a first temporary mixture;
  • (b) treating the first temporary mixture to obtain a basic solution including:
    • dissolving a quicklime (CaO) ingredient in solution concentrated HCl contains 40% (concentrated grade) with combined stirring at 50 rpm for 5 minutes to obtain a solution 1;
    • admixing the first temporary mixture to the solution 1 with combined stirring at 50 rpm for 5 minutes, then stop stirring and let stand for 7-10 days at 28° C.-40° C. to obtain the basic solution;
      • wherein a ratio of the first temporary mixture and the quicklime (CaO) ingredient is 1: (2-5) (w/w);
      • wherein a ratio of the quicklime (CaO) ingredient and the solution concentrated HCl contains 40% (concentrated grade) is 1: (2-5) (w/v);
  • (c) admixing 1 part of the enzyme solution into 10 parts of the basic solution, then stop stirring and let stand for 12-18 hours to obtain the chitin ingredient from shrimp shells.

Another objective of the present invention is to provide the chitin ingredient from oyster mushroom comprising performing in a specific order from (a′) to (d′):

• • (a′) collecting oyster mushrooms, then washing to remove impurities, and soaking with a fruit vinegar in a ratio of 1: (3-5) (w/v) for 15-20 days, then filtering to remove liquid, and washing twice with the rice alcohol has alcohol range 30%-50% to obtain a second temporary mixture; wherein the fruit vinegar has a concentration of 35%-55%;
  • (b′) treating the second temporary mixture to obtain a basic temporary solution including:
    • dissolving a quicklime (CaO) ingredient in solution concentrated HCl contains 40% (concentrated grade) with combined stirring at 50 rpm for 5 minutes to obtain the solution 1;
    • admixing the second temporary mixture to the solution 1 with combined stirring at 50 rpm for 5 minutes, then stop stirring and let stand for 7-10 days at 28° C.-40° C. to obtain the basic temporary solution;
      • wherein a ratio of the second temporary mixture and the quicklime (CaO) ingredient is 1: (3-5) (w/w);
      • wherein a ratio of the quicklime (CaO) ingredient and the solution concentrated HCl contains 40% (concentrated grade) is 1: (2-5) (w/v);
  • (c′) admixing a microorganism solution into the basic temporary solution at a ratio of (1-2): 10 (w/v) to obtain a foundation temporary solution; and
  • (d′) adjusting pH of the foundation temporary solution reached 6.8-7.2, then fermenting at 30° C.-40° C. for 125-135 hours to obtain the chitin temporary mixture from oyster mushroom.

Yet another objective of the present invention is to provide the fruit vinegar comprising performing in a specific order from (A′) to (G′):

• • (A′) selecting and preparing fruits by a predetermined quality guideline, includes selecting said fruits that have a Brix level of at highest 2; in which fruits are selected from the group consisting of ambarella (Spondias dulcis), plum (Prunus salicina), apricot (Prunus armeniaca (L.)), crocodile fruit (Dracontomelon duperreanum), star gooseberry (Phyllanthus acidus (L.)), and a combination thereof;
  • (B′) performing visual inspection to select undamaged fruits;
  • (C′) washing fruits, then cold-squeezing fruits to obtain a fruit juice;
  • (D′) creating a foundation solution by mixing the fruit juice and the coconut water in ratio of 1:3;
  • (E′) pasteurizing the foundation solution at 85° C. for 4 minutes, then let it cool, and adjusting the Brix to 6 to obtain a pasteurized solution;
  • (F′) adding ethanol 95% at a ratio of 3% (v/v) to the pasteurized solution, adjusting the pH to 5 by acetic acid 1.5%, then adding Acetobacter aceti bacteria in ratio of 1.2% (v/v), and fermenting for 7 days to obtain a solution after fermentation; and
  • (G′) filtering the solution after fermentation to obtain the fruit vinegar.

In view of the foregoing, another objective of the present invention is to the rice alcohol has alcohol range 30%-50% obtained by fermenting a homogeneous mixture twice, then distilling and aging the alcohol using an alcohol aged machine or alcohol aging equipment;

• • wherein the homogeneous mixture includes 600 parts of a cooked rice mixture, and (1-2) parts of a wine yeast ingredient;
    • the cooked rice mixture is cooked from 3 parts glutinous rice with 1 part plain rice, 0.2 part shelled green beans, and 4.5 parts water;
  • wherein the wine yeast ingredient includes 11 parts of a rice flour, (0.6-0.8) parts of an extracted herbal, and (0.001-0.1) parts of a yeast ingredient;
    • the extracted herbal is extracted from a herbal mixture crushed/chopped, and soaked in solvent, or saturated brine solution; the herbal mixture comprising: Myristica fragrans Houtt., Curcuma aromatica Salisb., Atractylodes macrocephala Koidz., Mentha arvensis L., Amomum aromaticum Roxb., Glycyrrhiza uralensis Fisch., Foeniculum vulgare Mill., Illicium verum Hook. f., and Cortex Cinnamomi cassiae;
    • the yeast ingredient is selected from the group consisting of Saccharomyces cerevisiae NH2, Saccharomyces cerevisiae NT3, Saccharomyces cerevisiae MS42, Saccharomyces cerevisiae CM3.2, Saccharomyces cerevisiae D8, Saccharomyces cerevisiae NM11, and Candida tropicalis NM2.

Finally, the purpose of the invention is to provide the microorganism solution comprising performing in a specific order from (A) to (E):

• • (A) creating a first suspension solution comprising performing in a specific order from (a1) to (c1):
    • (a1) activating Bacillus sp. TV11 on the Nutrient agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Bacillus sp. TV11;
    • (b1) inoculating a single colony of the activated Bacillus sp. TV11 into a test tube containing 10 ml of Nutrient broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased first biomass solution; and
    • (c1) inoculating the increased first biomass solution into Nutrient broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the first suspension solution;
  • (B) creating a second suspension solution comprising performing in a specific order from (a2) to (c2):
    • (a2) activating Lactobacillus sp. T432 on the Man Rogosa Sharpe (MRS) agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Lactobacillus sp. T432;
    • (b2) inoculating a single colony of the activated Lactobacillus sp. T432 into a test tube containing 10 ml of MRS broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased second biomass solution; and
    • (c2) inoculating the increased second biomass solution into MRS broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the second suspension solution;
  • (C) creating a third suspension solution comprising performing in a specific order from (a3) to (c3):
    • (a3) activating Lactobacillus plantarum VTCC 431 on the MRS agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Lactobacillus plantarum VTCC 431;
    • (b3) inoculating a single colony of the activated Lactobacillus plantarum VTCC 431 into a test tube containing 10 ml of MRS broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased third biomass solution; and
    • (c3) inoculating the increased third biomass solution into MRS broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the third suspension solution;
  • (D) creating a fourth suspension solution comprising performing in a specific order from (a4) to (c4):
    • (a4) activating Lactobacillus bulgaricus VTCC 703 on the MRS agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Lactobacillus bulgaricus VTCC 703;
    • (b4) inoculating a single colony of the activated Lactobacillus bulgaricus VTCC 703 into a test tube containing 10 ml of MRS broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased fourth biomass solution; and
    • (c4) inoculating the increased fourth biomass solution into MRS broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the fourth suspension solution;
  • (E) mixing (1-2) parts of the first suspension solution with (1-2) parts of the second suspension solution, (1-2) parts of the third suspension solution, and (1-2) parts of the fourth suspension solution to obtain the microorganism solution.

These and other advantages of the present invention will no doubt become obvious to those of ordinary skill in the art after having read the following detailed description of the preferred embodiments, which are illustrated in the various drawing Figures.

BRIEF DESCRIPTION OF THE DRAWING

The accompanying drawings, which are incorporated in and form a part of this specification, illustrate embodiments of the invention and, together with the description, serve to explain the principles of the invention.

FIG. 1 is a flowchart illustrating a method of manufacturing the chitosan composition according to an embodiment of the present invention;

FIG. 2 is a flowchart illustrating a process for preparing the microorganism solution according to an embodiment of the present invention; and

FIG. 3 is a flowchart illustrating a process for preparing the fruit vinegar according to an embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Reference will now be made in detail to the preferred embodiments of the invention, examples of which are illustrated in the accompanying drawings. While the invention will be described in conjunction with the preferred embodiments, it will be understood that they are not intended to limit the invention to these embodiments. On the contrary, the invention is intended to cover alternatives, modifications, and equivalents, which may be included within the spirit and scope of the invention as defined by the appended claims.

Furthermore, in the following detailed description of the present invention, numerous specific details are set forth in order to provide a thorough understanding of the present invention. However, it will be obvious to one of ordinary skill in the art that the present invention may be practiced without these specific details. In other instances, well-known methods, procedures, components, and circuits have not been described in detail so as not to unnecessarily obscure aspects of the present invention.

It should also be noted that the term “dissolve/dissolving/dissolved” is used in the invention understood to mean the uniform distribution, or complete dissolution of, substances present in a solution/mixture.

One embodiment of the invention is now described with reference to FIG. 1. FIG. 1 illustrating a specific process of manufacturing the chitosan composition 100 (“method 100”) based on the above principle in accordance with an exemplary embodiment of the present invention. In particular, method 100 includes the following steps:

At step 110, prepare materials including: a microorganism solution, a fruit vinegar, an enzyme solution, and a rice alcohol that has alcohol range 30%-50%.

According to the embodiment of the invention, the microorganism solution obtained from a process 200 will be described in detail later below. The fruit vinegar obtained from a process 300 will be described in detail later below.

According to the embodiment of the invention, prepare the enzyme solution by performing steps from (A″) to (B″) including:

• • (A″) creating an enzyme preparation by homogeneously mixing (1-3) parts of a protease ingredient with 1 part of a lipase ingredient; and
  • (B″) creating the enzyme solution by homogeneously mixing (3-5) parts of the enzyme preparation with (5000-10000) parts of the water.

According to the embodiment of the invention, prepare the rice alcohol has alcohol range 30%-50% by fermenting a homogeneous mixture twice, then distilling and aging the alcohol using an alcohol aged machine or alcohol aging equipment.

According to the preferred embodiment of the present invention, the rice alcohol has alcohol range 45%-50%.

According to the embodiment of the invention, the homogeneous mixture includes 600 parts of a cooked rice mixture, and (1-2) parts of a wine yeast ingredient.

According to the preferred embodiment of the invention, the cooked rice mixture is cooked from 3 parts glutinous rice with 1 part plain rice, 0.2 part shelled green beans, and 4.5 parts water.

According to the embodiment of the invention, the wine yeast ingredient includes 11 parts of a rice flour, (0.6-0.8) parts of an extracted herbal, and (0.001-0.1) parts of a yeast ingredient.

According to the embodiment of the invention, the wine yeast ingredient includes 11 parts of the rice flour, (0.6-0.8) parts of the extracted herbal, and (0.01-0.1) parts of the yeast ingredient.

According to the preferred embodiment of the invention, the wine yeast ingredient includes 11 parts of the rice flour, 0.7 parts of the extracted herbal, and (0.01-0.1) parts of the yeast ingredient.

According to the embodiment of the invention, the extracted herbal is extracted from a herbal mixture crushed/chopped, and soaked in solvent, or saturated brine solution. The herbal mixture is listed in Table 2 below, including: Myristica fragrans Houtt., Curcuma aromatica Salisb., Atractylodes macrocephala Koidz., Mentha arvensis L., Amomum aromaticum Roxb., Glycyrrhiza uralensis Fisch., Foeniculum vulgare Mill., Illicium verum Hook. f., and Cortex Cinnamomi cassiae.

TABLE 2
Components of the herbal mixture are used
in the embodimentof the present invention

No.	Species	Collection region	Used parts
1	Myristica fragrans Houtt.	Vietnam	seeds
2	Curcuma aromatica Salisb.		rhizomes
3	Atractylodes macrocephala Koidz.		rhizomes
4	Mentha arvensis L.		leaves
5	Amomum aromaticum Roxb.		fruits
6	Glycyrrhiza uralensis Fisch.		rhizomes
7	Foeniculum vulgare Mill.		fruits
8	Illicium verum Hook. f.		fruits
9	Cortex Cinnamomi cassiae		bark

According to the embodiment of the invention, the yeast ingredient is selected from the group consisting of Saccharomyces cerevisiae NH2, Saccharomyces cerevisiae NT3, Saccharomyces cerevisiae MS42, Saccharomyces cerevisiae CM3.2, Saccharomyces cerevisiae D8, Saccharomyces cerevisiae NM11, and Candida tropicalis NM2; all are listed in Table 3 below.

TABLE 3
The strains of yeasts present in the yeast ingredient according
to the embodiment of the invention

No.	Type species	Storage location	Reference
1	Saccharomyces	Institute of	Bình, L. N., Thành, N. V., Th  o, H. P.,
	cerevisiae NH2	Biotechnology	& Khánh, T. V. (2015). Isolating and
2	Saccharomyces	Research and	screening strongly active yeast
	cerevisiae NT3	Development, Can	strains from local alcoholic
		Tho University	fermentation starters. CTU Journal of
			Science and Technology, (39), 18-28.
3	Saccharomyces	Institute of	Nguy  n V  n Quyên et al (2018).
	cerevisiae MS42	Biotechnology and	The influence of some factors on the
		Food Industry, Hanoi	production of alcohol whisky by
		University of Science	Saccharomyces cerevisiae MS42
		and Technology	from barley malt. Journal of
			Biotechnology 16(3), 525-532.
4	Saccharomyces	Institute of	Ðoàn Th   Ki  u Tiên el al (2018).
	cerevisiae CM3.2	Biotechnology	Evaluation of total polyphenol and
		Research and	antioxidant capacity in wine
		Development, Can	fermentation of three-leaf cayratia
		Tho University	from Ca Mau province using
			Saccharomyces cerevisiae CM3.2.
			CTU Journal of Science and
			Technology, 55 (2), 285-291.
5	Saccharomyces	Institute of	Le Thuong, H. T., Thuy, T. T., & Hao,
	cerevisiae D8	Biotechnology	N. Q. (2018). Improvement of the
		Research and	ethanol production of saccharomyces
		Development, Tan	cerevisiae D8 by the random
		Trao University	mutagenesis. Vietnam Journal of
			Biotechnology, 16(2), 337-344.
6	Saccharomyces	Institute of	Ð   Th   Bích Th  y et al (2023). Effect
	cerevisiae NM11	Biotechnology	of some factors on the content of the
		Research and	Compounds in watermelon juice
		Development, Hue	fermented by Saccharomyces
		University	cerevisiae NM11. Journal of
			Agricultural Science and Technology.
7	Candida tropicalis	Institute of	Doan Van Thuoc et al (2015).
	NM2	Biotechnology	Characterization of alcohol producing
		Research and	yeast isolated from fermented fruit
		Development, Hanoi	juice of sonneratia caseolaris.
		National University of	Vietnam Journal of Biotechnology,
		Education	37(1), 69-75.

The term “homogeneous/homogeneously” is understood to mean the uniform distribution, or complete dissolution of, substances present in a solution/mixture.

At step 120, creating a chitin ingredient from shrimp shells comprising performing in a specific order from (a) to (c):

• • (a) collecting a molting shell of shrimp, then washing to remove impurities, and soaking with HCl solution in a ratio of 1: (3-5) (w/v) for 15-20 days, then filtering to remove liquid, washing twice with the rice alcohol has alcohol range 30%-50 to obtain a first temporary mixture; in which HCl solution obtained by diluting a solution concentrated HCl contains 40% (concentrated grade) with water to 5%-18% HCl solution;
  • (b) treating the first temporary mixture to obtain a basic solution including:
    • dissolving a quicklime (CaO) ingredient in solution concentrated HCl contains 40% (concentrated grade) with combined stirring at 50 rpm for 5 minutes to obtain a solution 1;
    • admixing the first temporary mixture to the solution 1 with combined stirring at 50 rpm for 5 minutes, then stop stirring and let stand for 7-10 days at 28° C.-40° C. to obtain the basic solution;
      • wherein a ratio of the first temporary mixture and the quicklime (CaO) ingredient is 1: (2-5) (w/w);
      • wherein a ratio of the quicklime (CaO) ingredient and solution concentrated HCl contains 40% (concentrated grade) is 1: (2-5) (w/v);
  • (c) admixing 1 part of the enzyme solution at step 110 into 10 parts of the basic solution, then stop stirring and let stand for 12-18 hours to obtain the chitin ingredient from shrimp shells.

According to the priority embodiment of the invention, at step (b) the ratio of the first temporary mixture and the quicklime (CaO) ingredient is 1:3 (w/w).

According to the embodiment of the invention, the molting shell of shrimp is selected from the group consisting of litopenaeus vannamei (Penaeus vannamei), Penaeus monodon, Penaeus merguiensis, Macrobrachium rosenbergii, Metapenaeus ensis, Macrobrachium lanchesteri, Fenneropenaeus merguiensis, Penaeus semisulcatus, and a combination thereof; all are listed in Table 4 below.

TABLE 4
Ingredients of shrimp species present in the shrimp shells
according to the embodiment of the invention

			Time to raise fully
No.	Species	Collection region	mature shrimp

1	litopenaeus	Mekong Delta region: Soc Trang, Bac Lieu,	180 days
	vannamei	Ca Mau, Kien Giang, Tra Vinh provinces;
	(Penaeus	Central region: Binh Dinh, Phu Yen, Khanh
	vannamei)	Hoa, Ninh Thuan, Binh Thuan provinces;
		Southeast region: Ba Ria-Vung Tau, Tien
		Giang, Long An provinces;
		Northern region: Quang Ninh, Thai Binh,
		Nam Dinh provinces.
2	Penaeus	Mekong Delta region: Ca Mau, Bac Lieu,	4 months
	monodon	Kien Giang, Tra Vinh, Soc Trang, An Giang,
		Tien Giang provinces;
		Central Coast region: Binh Dinh, Phu Yen,
		Ninh Thuan, Binh Thuan provinces;
		North Central region: Thanh Hoa, Nghe An,
		Ha Tinh provinces;
		Southeast region: Ba Ria-Vung Tau, Dong
		Nai provinces;
		Northern region: Thai Binh, Nam Dinh,
		Quang Ninh provinces.
3	Penaeus	Mekong Delta region: Ca Mau, Bac Lieu,	3-4 months
	Merguiensis	Tra Vinh, Soc Trang, An Giang, Kien Giang
		provinces;
		Central Coast region: Binh Dinh, Phu Yen,
		Khanh Hoa, Ninh Thuan, Binh Thuan
		provinces;
		Southeast region: Ba Ria-Vung Tau, Tien
		Giang, Long An provinces.
4	Macrobrachium	Ca Mau, Kien Giang, Can Tho, Long An,	100-135 days
	rosenbergii	Dong Nai, Ben Tre, Soc Trang, An Giang
		provinces.
5	Metapenaeus	Mekong Delta region: Ca Mau, Bac Lieu,	3-4 months
	ensis	Tra Vinh, Soc Trang, An Giang, Kien Giang
		provinces;
		Central Coast region: Binh Dinh, Phu Yen,
		Khanh Hoa, Ninh Thuan, Binh Thuan
		provinces;
		Southeast region: Ba Ria-Vung Tau, Tien
		Giang, Long An provinces.
6	Macrobrachium	North:	3-4 months
	lanchesteri	Red River Basin (Hanoi, Hai Phong, Hai
		Duong provinces);
		Thai Binh river basin (Thai Binh, Nam Dinh
		provinces);
		Cau River basin (Bac Giang, Bac Ninh
		provinces);
		Central region:
		Ma River basin (Thanh Hoa province);
		Gianh river basin (Quang Binh province);
		Vu Gia-Thu Bon river basin (Quang Nam,
		Da Nang province);
		Southern:
		Dong Nai River Basin (Dong Nai province,
		Ho Chi Minh City);
		Tien and Hau river basins (Mekong Delta);
		Coastal lagoon area (Ca Mau, Kien Giang
		province).
7	Fenneropenaeus	Mekong Delta region: Ca Mau, Bac Lieu,	3-4 months
	Merguiensis	Tra Vinh, Soc Trang, An Giang, Kien Giang
		provinces;
		Central Coast region: Binh Dinh, Phu Yen,
		Khanh Hoa, Ninh Thuan, Binh Thuan
		provinces;
		Southeast region: Ba Ria-Vung Tau, Tien
		Giang, Long An provinces.
8	Penaeus	Mekong Delta region: Ca Mau, Bac Lieu,	3-4 months
	Semisulcatus	Tra Vinh, Soc Trang, An Giang, Kien Giang
		provinces;
		Central Coast region: Binh Dinh, Phu Yen,
		Khanh Hoa, Ninh Thuan, Binh Thuan
		provinces;
		Southeast region: Ba Ria-Vung Tau, Tien
		Giang, Long An provinces.

According to the embodiment of the invention, the molting shell of shrimp is a molting shell of shrimp from 60-180 days old shrimp.

According to the embodiment of the invention, the molting shell of shrimp is a molting shell of shrimp from 61-90 days old shrimp.

According to the embodiment of the invention, the molting shell of shrimp is a molting shell of shrimp from 71-80 days old shrimp.

Refer to the survey results of chitin, mineral and protein content analyzed from molting shrimp shells at different age stages (01-06), all listed in Table 5 below.

TABLE 5
Comparison of chitin, mineral and protein content analyzed
from molting shrimp shells at different age stages (O1-O6)
according to the invention's embodiment

Species	Stages	Age (days)	Minerals (%)	Protein (%)	Chitin (%)
litopenaeus vannamei	O1	31-60	54.95 ± 2.6	12.45 ± 1.1	20.1 ± 0.8
(Penaeus vannamei)	O2	61-70	60.8 ± 1.9	10.4 ± 0.7	23.4 ± 0.5
	O3	71-80	53.5 ± 0.5	12.6 ± 0.6	23.7 ± 0.2
	O4	81-90	55.1 ± 0.8	12.5 ± 0.8	23.5 ± 0.7
	O5	>90	55.8 ± 1.9	12.7 ± 0.7	23.6 ± 0.5
Penaeus monodon	O1	31-60	53.66 ± 2.2	11.75 ± 1.3	19.5 ± 0.6
	O2	61-70	62.8 ± 1.4	9.84 ± 0.5	22.7 ± 0.8
	O3	71-80	52.2 ± 0.7	11.6 ± 0.6	22.5 ± 0.3
	O4	81-90	54.5 ± 0.6	11.8 ± 0.4	22.1 ± 0.2
	O5	>90	54.7 ± 1.3	11.95 ± 0.7	22.3 ± 0.6
Penaeus Merguiensis	O1	31-60	55.45 ± 1.7	12.55 ± 1.2	20.8 ± 0.5
	O2	61-70	61.9 ± 1.1	10.3 ± 0.9	24.1 ± 0.3
	O3	71-80	52.7 ± 0.6	13.2 ± 0.4	24.9 ± 0.2
	O4	81-90	56.2 ± 0.1	13.4 ± 0.5	24.6 ± 0.3
	O5	>90	56.5 ± 1.5	13.6 ± 0.2	24.5 ± 0.7
Macrobrachium	O1	31-60	54.12 ± 1.9	11.97 ± 1.5	20.5 ± 0.2
rosenbergii	O2	61-70	63.4 ± 1.8	9.76 ± 0.8	23.5 ± 0.4
	O3	71-80	53.5 ± 0.6	11.8 ± 0.5	23.8 ± 0.7
	O4	81-90	54.8 ± 0.7	11.7 ± 0.8	23.4 ± 0.4
	O5	>90	54.9 ± 1.1	11.9 ± 0.3	23.3 ± 0.8
Metapenaeus ensis	O1	31-60	56.1 ± 1.2	13.11 ± 1.3	21.6 ± 0.7
	O2	61-70	61.3 ± 1.4	11.3 ± 0.4	23.1 ± 0.4
	O3	71-80	53.9 ± 0.5	13.8 ± 0.7	23.7 ± 0.9
	O4	81-90	55.7 ± 0.7	13.5 ± 0.3	23.4 ± 0.7
	O5	>90	55.9 ± 1.4	13.7 ± 0.6	23.3 ± 0.3
Macrobrachium	O1	31-60	55.84 ± 1.6	12.45 ± 1.6	21.2 ± 0.7
lanchesteri	O2	61-70	64.5 ± 1.2	10.63 ± 0.7	24.2 ± 0.3
	O3	71-80	54.1 ± 0.4	12.6 ± 0.8	24.9 ± 0.4
	O4	81-90	55.2 ± 0.5	12.4 ± 0.6	24.6 ± 0.7
	O5	>90	54.4 ± 1.3	12.7 ± 0.5	24.7 ± 0.5
Fenneropenaeus	O1	31-60	54.77 ± 2.0	12.25 ± 1.3	20.3 ± 0.7
Merguiensis	O2	61-70	60.5 ± 1.5	10.1 ± 0.5	23.2 ± 0.7
	O3	71-80	53.8 ± 0.4	12.9 ± 0.3	23.8 ± 0.6
	O4	81-90	55.3 ± 0.9	12.4 ± 0.6	23.4 ± 0.6
	O5	>90	55.7 ± 1.7	12.6 ± 0.8	23.5 ± 0.4
Penaeus Semisulcatus	O1	31-60	55.5 ± 1.8	12.65 ± 1.6	20.8 ± 0.5
	O2	61-70	61.7 ± 1.1	10.5 ± 0.6	22.6 ± 0.2
	O3	71-80	54.4 ± 0.3	12.7 ± 0.8	22.9 ± 0.8
	O4	81-90	56.2 ± 0.8	12.2 ± 0.5	22.5 ± 0.6
	O5	>90	56.5 ± 1.4	12.4 ± 0.7	22.7 ± 0.4

At step 130, creating a chitin ingredient from oyster mushroom comprising performing in a specific order from (a′) to (d′):

• • (a′) collecting oyster mushrooms, then washing to remove impurities, and soaking with the fruit vinegar at step 110 in a ratio of 1: (3-5) (w/v) for 15-20 days, then filtering to remove liquid, and washing twice with the rice alcohol has alcohol range 30%-50% to obtain a second temporary mixture; wherein the fruit vinegar has a concentration of 35%-55%;
  • (b′) treating the second temporary mixture to obtain a basic temporary solution including:
    • dissolving the quicklime (CaO) ingredient in solution concentrated HCl contains 40% (concentrated grade) with combined stirring at 50 rpm for 5 minutes to obtain the solution 1;
    • admixing the second temporary mixture to the solution 1 with combined stirring at 50 rpm for 5 minutes, then stop stirring and let stand for 7-10 days at 28° C.-40° C. to obtain the basic temporary solution;
      • wherein a ratio of the second temporary mixture and the quicklime (CaO) ingredient is 1: (3-5) (w/w);
      • wherein a ratio of the quicklime (CaO) ingredient and solution concentrated HCl contains 40% (concentrated grade) is 1: (2-5) (w/v);
  • (c′) admixing the microorganism solution at step 110 into the basic temporary solution at a ratio of (1-2): 10 (w/v) to obtain a foundation temporary solution; and
  • (d′) adjusting pH of the foundation temporary solution reached 6.8-7.2, then fermenting at 30° C.-40° C. for 125-135 hours to obtain the chitin temporary mixture from oyster mushroom.

According to the priority embodiment of the invention, at step (b′) the ratio of the second temporary mixture and the quicklime (CaO) ingredient is 1:4 (w/w).

According to another embodiment of the invention, replacing the quicklime (CaO) ingredient with a solution lime for betel chewing. The solution lime for betel chewing is obtained by dissolving 1 part of a powdered lime for betel chewing with 0.5-5 parts of the water; wherein the powdered lime for betel chewing is obtained by calcining (burning) shells, coral, or limestone. The powdered lime for betel chewing comprising chemical components: calcium hydroxide Ca(OH)₂, and calcium carbonate CaCO₃.

According to the embodiment of the invention, oyster mushrooms listed in Table 6 below, including: Pleurotus pulmonarius, Pleurotus cf. floridanus, Pleurotus ostreatus, Pleurotus citrinopileutus, and a combination thereof.

TABLE 6
Ingredients of species present in the oyster mushrooms
according to the embodiment of the invention

No.	Species	References
1	Pleurotus	Pham Van Loc et al (2023). Identification of
	pulmonarius	Oyster Mushroom (Pleurotus spp.) Strains in
2	Pleurotus cf.	the South Vietnam based on Morphological
	floridanus	Characteristics and ITS Sequencing. Vietnam J.
3	Pleurotus	Agri. Sci, 21(12): 1569-1580
	ostreatus
4	Pleurotus	Nguyen Thi Thom et al (2018). Study of
	citrinopileatus	cultivating golden oyster mushroom Pleurotus
		citrinopileatus utilization of agricultural waste.
		Journal of Science. University of Education,
		Hue University, 01(45): 138-148

At step 140, creating a chitin mixture by homogenously mixing the chitin ingredient from shrimp shells at step 120 with the chitin ingredient from oyster mushroom at step 130; wherein a ratio of the chitin ingredient from shrimp shells and the chitin ingredient from oyster mushroom is (1-10): 1 (w/w).

According to the embodiment of the invention, the ratio of the chitin ingredient from shrimp shells and the chitin ingredient from oyster mushroom is (1-7): 1 (w/w).

According to the embodiment of the invention, the ratio of the chitin ingredient from shrimp shells and the chitin ingredient from oyster mushroom is (1-5): 1 (w/w).

According to the embodiment of the invention, the ratio of the chitin ingredient from shrimp shells and the chitin ingredient from oyster mushroom is (1-3): 1 (w/w).

At step 150, loading the chitin mixture into a centrifugal spray drying device having predetermined specifications to create the chitosan composition; in which predetermined specifications include: a rotate speed of 1200 rpm for 3-5 hours at temperature 20° C.-28° C. Step 150 can be done with the centrifugal spray drying device and other similar devices. The centrifugal spray drying device has been known in previous art so the description of the structure and its operating principle will not be described in detail in the invention.

According to the embodiment of the invention, at step 150, the chitosan composition has a pH of 7-8.5.

According to the embodiment of the invention, at step 150, the chitosan composition has a pH of 8-8.5.

According to the embodiment of the invention, at step 150, time is 4-5 hours.

According to the embodiment of the invention, at step 150, time is 5 hours.

According to the embodiment of the invention, at step 150, temperature is 23° C.-26° C.

According to the embodiment of the invention, at step 150, temperature is 25° C.

Finally, at step 160, packaging the chitosan composition at step 150 and preservation.

According to other embodiments of the invention, the method 100 further comprising step drying the chitosan composition at 70° C. for 5-10 minutes before the step 160 packaging and preservation.

According to the invention, the chitosan composition obtained by method 100 is edible and soluble in saliva secreted in the oral cavity by more than 95%, preferably more than 97%, preferably more than 98%.

It should be noted that the term “admixed/mixed/admixing/mixing” as used in the present invention is understood to mean adding, or reacting, or dissolving homogeneously, or evenly, components in the same solution/mixture.

Now referring to FIG. 2, the process for preparing the microorganism solution 200 (“process 200”) based on the above principle in accordance with an exemplary embodiment of the present invention. In particular, process 200 includes the following steps:

At step 201, creating a first suspension solution comprising performing in a specific order from (a1) to (c1):

• • (a1) activating Bacillus sp. TV11 on the Nutrient agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Bacillus sp. TV11;
  • (b1) inoculating a single colony of the activated Bacillus sp. TV11 into a test tube containing 10 ml of Nutrient broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased first biomass solution; and
  • (c1) inoculating the increased first biomass solution into Nutrient broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the first suspension solution.

At step 202, creating a second suspension solution comprising performing in a specific order from (a2) to (c2):

• • (a2) activating Lactobacillus sp. T432 on the Man Rogosa Sharpe (MRS) agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Lactobacillus sp. T432;
  • (b2) inoculating a single colony of the activated Lactobacillus sp. T432 into a test tube containing 10 ml of MRS broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased second biomass solution; and
  • (c2) inoculating the increased second biomass solution into MRS broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the second suspension solution.

At step 203, creating a third suspension solution comprising performing in a specific order from (a3) to (c3):

• • (a3) activating Lactobacillus plantarum VTCC 431 on the MRS agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Lactobacillus plantarum VTCC 431;
  • (b3) inoculating a single colony of the activated Lactobacillus plantarum VTCC 431 into a test tube containing 10 ml of MRS broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased third biomass solution; and
  • (c3) inoculating the increased third biomass solution into MRS broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the third suspension solution.

At step 204, creating a fourth suspension solution comprising performing in a specific order from (a4) to (c4):

• • (a3) activating Lactobacillus plantarum VTCC 431 on the MRS agar medium, incubating at 37° C. for a period of 36-48 hours to obtain an activated Lactobacillus plantarum VTCC 431;
  • (b3) inoculating a single colony of the activated Lactobacillus plantarum VTCC 431 into a test tube containing 10 ml of MRS broth medium, shaking at 200 rpm for 24 hours at 37° C. to obtain an increased third biomass solution; and
  • (c3) inoculating the increased third biomass solution into MRS broth medium at a ratio of (1-3): 100, shaking at 200 rpm for 24 hours at 37° C. to obtain the third suspension solution.

Finally, at step 205, mixing (1-2) parts of the first suspension solution at step 201 with (1-2) parts of the second suspension solution at step 202, (1-2) parts of the third suspension solution at step 203, and (1-2) parts of the fourth suspension solution at step 204 to obtain the microorganism solution.

According to the embodiment of the present invention, the microorganism solution contains strains of microorganisms including Bacillus sp. TV11, Lactobacillus sp. T432, Lactobacillus plantarum VTCC 431, and Lactobacillus bulgaricus VTCC 703, all listed in Table 7 below.

TABLE 7
The strains of microorganisms present in the microorganism
solution according to the embodiment of the invention

Genus	Type species	Storage location	Reference
Bacillus	Bacillus sp.	Institute of	Phong, H. X., Linh, L. Ð., Nam,
	TV11	Biotechnology	P. H., Thanh, N. N., & Long, B.
Lactobacillus	Lactobacillus	Research and	H. Ð. (2020). Production of
	sp. T432	Development, Can	chitin from shrimp shells
		Tho University	(Penaeus monodon) using
			Bacillus sp. TV11 and
			Lactobacillus sp. T342. TNU
			Journal of Science and
			Technology, 225(08), 230-238.
	Lactobacillus	Vietnam Type	Boi, V. N., Trang, N. T. M.,
	plantarum	Culture Collection-	Thao, N., T., P., Chung, L., P.,
	VTCC 431	Vietnam National	Yen, H., T., B. (2016). Study on
	Lactobacillus	University, Hanoi	using lactic acid bacteria for
	bulgaricus		demineralization and
	VTCC 703		deproteinization of heads and
			shells of shrimp in chitosan
			production. Journal of Fisheries
			Science and Technology (01),
			11-19.

Referring to FIG. 3, the process for preparing the fruit vinegar 300 (“process 300”) based on the above principle in accordance with an exemplary embodiment of the present invention. In particular, process 300 includes the following steps:

At step 301, selecting and preparing fruits by a predetermined quality guideline, includes selecting said fruits that have a Brix level of at highest 2.

According to the embodiment of the invention, said fruits is selected from the group consisting of ambarella (Spondias dulcis), plum (Prunus salicina), apricot (Prunus armeniaca (L.)), crocodile fruit (Dracontomelon duperreanum), star gooseberry (Phyllanthus acidus (L.)), and a combination thereof, all listed in Table 8 below.

TABLE 8
The fruits ingredients for creating the fruit vinegar according to the
embodiment of the present invention

Fruits	Scientific name	Collection region	Used part
Ambarella	Spondias dulcis	Central Vietnam	Fruit
Plum	Prunus salicina	Southern Vietnam
Apricot	Prunus armeniaca (L.)	Northern Vietnam
Crocodile fruit/	Dracontomelon	Northern Vietnam
Dracontomelon	duperreanum
Star gooseberry	Phyllanthus acidus (L.)	Northern Vietnam

At step 302, performing visual inspection to select undamaged fruits.

At step 303, washing fruits and cold-squeezing fruits to obtain a fruit juice.

At step 304, creating a foundation solution by mixing the fruit juice at step 303 and the coconut water in a ratio of 1:1.

At step 305, pasteurizing the foundation solution at step 304 at 85° C. for 4 minutes, then let it cool, and adjusting the Brix to 6 to obtain a pasteurized solution.

At step 306, adding ethanol 95% at a ratio of 3% (v/v) to the pasteurized solution at step 305, adjusting the pH to 5 by acetic acid 1.5%, then adding Acetobacter aceti bacteria in ratio of 1, 2% (v/v), and fermenting for 7 days to obtain a solution after fermentation.

Finally, at step 307, filtering the solution after fermentation at step 306 to obtain the fruit vinegar.

In the present invention and the specification of the present application, it should also be noted that the steps washing by distilled water according to method 100, or according to process 200, or according to process 300, all characterized in that the washing temperature of the distilled water is 55° C.-60° C. According to the preferred embodiment of the present invention, washing temperature of the distilled water is 60° C.

According to another embodiment of the invention, the chitosan composition created by method 100 is mixed with a turkey tail mushroom extract ingredient to obtain a complex composition of turkey tail mushroom extract-chitosan.

According to another embodiment of the invention, the chitosan composition created by method 100 is mixed with a turkey tail mushroom extract ingredient, a carboxymethyl cellulose solution 0.375%, a alginate solution 0.375%, a potassium citrate solution, a AgNO₃ solution 0.37%, a Cu(NO₃) 2 solution 0.723%, a Zn(NO₃) 2 solution 3.085%, Co(NO₃) 2 solution 0.746%, a Fe(NO₃) 3 solution 2.5%, a glycerin ingredient, a vitamin E, a tartrazine ingredient 1%, a K₂HPO₄ solution 15%, a mixture extracts/essential oils, and an other ingredient to obtain a composition for prevention and treatment of Early Mortality Syndrome (EMS) shrimp.

The purpose of the following example is to prove that the technical solution in this invention has been successfully researched and tested by the author. Specifically, according to the method 100 applied to create the chitosan composition including the following specific steps:

• • (Step 1) creating the chitin ingredient from shrimp shells is similar to step 120, characteristic in that:
    • at step (a), the soaking ratio between the molting shell of shrimp and HCl solution is 1:5 for 20 days;
    • at step (b):
      • the ratio of the quicklime (CaO) ingredient and the solution concentrated HCl contains 40% (concentrated grade) is 1:2 (w/v);
      • the soaking ratio between the first temporary mixture and the quicklime (CaO) ingredient is 1:3 (w/v); and
    • at step (c), time for let stand is 15 hours; and
  • (Step 2) creating the chitin ingredient from oyster mushroom is similar to step 130, characteristic in that:
    • at step (a′), the soaking ratio between oyster mushroom and the fruit vinegar is 1:5 for 15 days;
    • at step (b′):
      • the ratio of the quicklime (CaO) ingredient and the solution concentrated HCl contains 40% (concentrated grade) is 1:2 (w/v);
      • the soaking ratio between the second temporary mixture and the quicklime (CaO) ingredient is 1:4 (w/v); and
    • at step (c′), the mixing ratio between the microorganism solution and the second temporary mushroom powder is 1.5:10 (w/v); and
    • at step (d′), fermenting time is 130 hours;
  • (Step 3) creating the chitin mixture by homogenously mixing the chitin ingredient from shrimp shells with the chitin ingredient from oyster mushroom is similar to step 140, including five formulas listed in Table 9 below;
  • (Step 4) creating the chitosan composition is similar to step 150, characteristic in that predetermined specifications including: a rotate speed of 1200 rpm for 5 hours at temperature 25° C.

TABLE 9
Ratio of mixing ingredients for creating the chitin mixture in five
formulas according to method 100 of the present invention

Ratio (w/w)

	The chitin ingredient	The chitin ingredient
Formula	from shrimp shells	from oyster mushroom

1	1	1
2	3	1
3	5	1
4	7	1
5	10	1

The present invention is further described in detail with reference to the following the ratio (w/w or v/v) of mixing ingredients to create the microorganism solution according to process 200 including fifteen formulas listed in Table 10 below.

TABLE 10
Ratio of mixing ingredients for creating the microorganism solution
in fifteen formulas according to process 200 of the present invention

Ratio (w/w or v/v)

	The first	The second	The third	The fourth
	suspension	suspension	suspension	suspension
Formula	solution	solution	solution	solution

1	1	1	1	1
2	1	1	1	2
3	1	1	2	1
4	1	2	1	1
5	2	1	1	1
6	2	1	1	2
7	2	1	2	1
8	2	2	1	1
9	1	1	2	2
10	1	2	1	2
11	1	2	2	1
12	2	2	2	1
13	2	2	1	2
14	2	1	2	2
15	1	2	2	2

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “includes” and/or “including,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, element components, and/or groups thereof.

While the preferred embodiment to the invention had been described, it will be understood that those skilled in the art, both now and in the future, may make various improvements and enhancements which fall within the scope of the claims which follow. These claims should be construed to maintain the proper protection for the invention first described.

The description of the present invention has been presented for purposes of illustration and description but is not intended to be exhaustive or limited to the invention in the form disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the invention. The embodiment was chosen and described in order to best explain the principles of the invention and the practical application and to enable others of ordinary skill in the art to understand the invention for various embodiments with various modifications as are suited to the particular use contemplated.

The flow diagrams depicted herein are just one example. There may be many variations to this diagram or the steps (or operations) described therein without departing from the spirit of the invention. For instance, the steps may be performed in a differing order, or steps may be added, deleted, or modified. All of these variations are considered a part of the claimed invention.

While the preferred embodiment to the invention had been described, it will be understood that those skilled in the art, both now and in the future, may make various improvements and enhancements which fall within the scope of the claims which follow. These claims should be construed to maintain the proper protection for the invention first described.

The foregoing description details certain embodiments of the invention. It will be appreciated, however, that no matter how detailed the foregoing appears in text, the invention can be practiced in many ways. As is also stated above, it should be noted that the use of particular terminology when describing certain features or aspects of the invention should not be taken to imply that the terminology is being re-defined herein to be restricted to including any specific characteristics of the features or aspects of the invention with which that terminology is associated. The scope of the invention should therefore be construed in accordance with the appended claims and any equivalents thereof.