ENZYMATIC MODIFIED STARCH REVIEW1.

ENZYMATIC MODIFIED STARCH REVIEW
1. Introduction
Henrissat classified all enzymes which have activity on carbohydrates into a number of families according to amino acid and DNA homology. The enzymes which act on starch and its derivatives are classified into several of these families and may be viewed on the CAZY website (://afmb.cnrs-mrs.fr/ CAZY/) (Coutinho and Henrissat, 1999). Currently, this website includes 91 distinct families, of which families 4, 13, 31, 57, 70 and 77 include enzymes which show activity on starch or its derivatives. Although every family includes enzymes which show sequence similarity and contain a number of conserved amino acid residues which are specific to that family, each family also includes a number of different reaction specificities. This is also seen with the families which contain enzymes that act on starch. Family 13 includes enzymes with _amylase (EC 3.2.1.1), pullulanase (EC 3.2.1.41), isoamylase (EC 3.2.1.68), glucan branching (EC 2.4.1.18) and cyclodextrin glycosyltransferase (EC 2.4.1.19) activities. Family 57 posseses _-amylase (EC 3.2.1.1), _-galactosidase (EC 3.2.1.22) and 4-_-glucanotransferase (EC 2.4.1.-) activities, while family 77 includes amylomaltase and 4-_-glucoantransferase (EC 2.4.1.-) activities. Family 4 contains many activities including maltose-6-phosphate glucosidase (EC 3.2.1.122), _-glucosidase (EC 3.2.1.20), _-galactosidase (EC 3.2.1.22), 6- phospho-_-glucosidase (EC 3.2.1.86) and _-glucuronidase (EC 3.2.1.139). Family 31 includes the following activities -glucosidase (EC 3.2.1.20); glucoamylase (EC 3.2.1.3); sucrase-isomaltase (EC 3.2.1.48) (EC 3.2.1.10); _-xylosidase (EC 3.2.1.-); _-glucan lyase (EC 4.2.2.13); isomaltosyltransferase (EC 2.4.1.-) (A5)

Fig. The enzymatic hydrolysis of starch and its derivatives. For reason of clarity not all activities and products are included
2. Starch granule degrading enzymes
Starch’s semi-crystalline nature, an ungelatinised starch granule is digested much more slowly by starch hydrolysing enzymes than a gelatinized granule or a starch solution. During hydrolysis a range of different morphologies may be observed, which range from pitting of small holes, shell formation, and surface erosion. The mode of enzymatic degradation is dependent both on the
Enzymatic treatment at sub-gelatinization temperature led to porous starch. Porous starch is attracting very much attention for its absorption and shielding ability in many food applications.
Highlight :
• α-amylase or amyloglucosidase action on corn starch was studied
• Pasting and thermal properties of porous starch depended on the enzyme used
• Porous starch was more susceptible to enzymatic digestion
Using enzyme: fungal α-amylase (AM) or amyloglucosidase (AMG)
α-Amylase can hydrolyze the (1→4) α-glucosidic bonds of starch in an endo-action. Hydrolysis occurs in a random fashion at any (1→4)-linkage within the starch chain to rapidly reduce the molecular size of starch and the viscosity of the starch solution during pasting.
Amyloglucosidase is an exo-acting enzyme that catalyzes the hydrolysis of both α-D-(1→4) and α-D-(1→6)-linkages from the non-reducing ends of the starch chain. Numerous researchers have investigated enzymatic hydrolysis of starches from cereals, roots, tubers, and legumes in terms of enzyme adsorption, action pattern, extent of hydrolysis, degree of crystallinity and hydrolysis products

Fig. Potato starch granules before (left) and after degradation by the amylases from Paenibacillus granivorans (middle) and Microbaterium aureum (right). (A5)
• Method
Method 1: Preliminary assays were carried out for optimizing enzymatic reactions (starch quantity and pH), and pH 4.0 was selected for AMG reaction and pH 6.0 in the case of AM modification. The quantity of enzymes was based on previous experiments, where the amount of enzyme required to hydrolyze 50% of the starch (15%, w/v) at 95ºC for 10 min was selected.
Starch (5.0 g) was suspended in 25 mL of 20mM NaH2PO4 buffer at pH 6.0 or in sodium acetate buffer at pH 4.0, those starch samples were referred as control-6 or control-4, respectively. For obtaining the enzymatic treated starches, enzymes (4 U of AMG /g starch and 5 U of AM /g starch) were added to the starch suspension. Samples were kept in a shaking water bath (50 rpm) at 50 ºC for 24 hours. Then, 50 mL of water were added and suspensions were homogenized. Samples were centrifuged for 15 min at 7,000×g and 4 ºC. Starches were washed again and centrifuged at the same conditions as before. Supernatants were pooled together and boiled in a water bath for 10 min to inactivate the enzymes before any further analyses (hydration properties and iodine binding values). Sediments containing starch were freeze-dried and kept at -25ºC for further thermal, biochemical and microstructural analyses. Four batches were prepared for each treatment (A2)
Method 2: Enzyme modification of starch was achieved using the enzyme α -amylase (Porcelain pancreatic amylase). 40% starch slurry was prepared by adding 40gm of starch to 100ml of distilled water, and enzyme (100µl) was added. The samples were allowed to stand at room temperature for 6 h. The flasks were then kept in the incubator at 50oC for 3h. After incubation, the supernatant was decanted and the starch was filtered and dried in the oven at 500 C. (A31)
3. Starch transferases
α 1,4-Glucanotransferases catalyse the cleavage of α-1,4 glucosidic bonds and the transfer of the newly formed reducing end group (donor) to a non-reducing saccharide unit (acceptor) with the formation of a new α -1,4 glucosidic bond. Donor and acceptor may originate from the same type of molecule or from different types of molecules. Several action patterns may be distinguished. Firstly, a single low molar mass maltooligosaccharide molecule may act both as donor and acceptor. In this case, cyclic saccharides are formed. Familiar examples are the cyclodextrins (CDs) with 6, 7, or 8 glucose units in the ring, which are formed by cyclodextrin glucosyltransferase. The net result of this type of activity is a decrease in the average molar mass. CDs are prepared by incubating a starch liquefact of DE < 10 with CGT-ase from Bacillus macerans (Riisgaard, 1990) or from thermostable microorganisms like Thermoanaerobacter species (Starnes, 1990). By addition of a complexing solvent, a crystalline inclusion complex is formed that can be separated from the mother liquor and refined by redissolution in water and recrystallisation. In a non-solvent process, the linear malto-oligosaccharides are degraded by amylolysis and cyclodextrin is recovered by partial evaporation and crystallisation. Like amylose, CDs have the ability to form crystalline complexes with a number of inclusion compounds. CDs have been widely explored as drug and flavour carriers (Szejtli, 1998). A novel development of randomly methylated α -CD is its use as an aid in emulsion polymerisation, e.g. in the surfactant-free production of polystyrene and polymethylmethacrylate latex particles in aqueous media (Storsberg et al., 2003). A different situation arises when the donor is transferred either to a different acceptor molecule or to a different side chain on the same molecule, e.g., in amylopectin. An interesting example is the so-called disproportioning enzyme or D-enzyme, also named amylomaltase because it catalyses the transfer of maltose from starch to glucose. A well known source of this enzyme is the potato, but a thermostable amylomaltase has also been isolated from Thermus thermophilus. Limited action of this enzyme on gelatinised starch leads to the progressive disappearance of amylose and the formation of amylopectin with a broader chain-length distribution. During this process the granular remnants dissolve completely and a low viscous molecular solution is obtained with a shift in iodine absorption maximum to lower wavelengths. Interestingly, these solutions form turbid rubber-like gels with a relatively high modulus on cooling at concentrations as low as 3%, which melt again on heating to c. 70oC. Amylomaltase-modified starch is a potential gelatin replacer in applications where gel transparency is not an issue. At higher conversions with this enzyme, cyclisation reactions on both linear and branched molecules occur, leading to relatively high molar mass starch products with a limited tendency to retrograde (Takaha et al., 1996, 1997).
A third situation arises when a different linkage type is formed during the transfer reaction. The action of starch branching enzyme (SBE) involves breaking of an -1,4-linkage and the concomitant formation of an -1,6-linkage. Thermostable branching enzymes have been isolated from a limited number of sources, e.g., Bacillus stearothermophilus.
The main effect is an overall reduction of amylopectin chain length, thereby reducing the propensity of starch to retrograde and increasing the solubility of starch in water. The fact that this action also results in the elimination of amylose and is not accompanied by the formation of maltose as a by-product makes SBE more useful than α-amylase. Involvement of a newly formed reducing end group into an α-1,6 linkage on the same molecule will also lead to the formation of cyclic molecules (Takata et al., 1996, 1997). (A5)

Fig1. Schematic representation of the reactions catalyzed hydrolases and transferases acting on starch. (M4)
3.1. Starch Branching Enzymes
The super-cluster structure of amylopectin (Gallant et al., 1997) might have evolved as a fitting strategy for plant survival and must be accomplished by well-refined regulation of a network of numerous enzyme actions. The fine structure of amylopectin is distinct from that of glycogen in animals and bacteria in that glycogen is randomly branched, the branches are more numerous, and the chains are shorter compared with amylopectin
Method :
Assay of starch Branching Enzymes.
The basis of the assay

Kết quả (Việt) 1:

ENZYM TINH BỘT LẦN XEM LẠI1. giới thiệuHenrissat phân loại tất cả enzym có hoạt động trên carbohydrate vào một số các gia đình theo axit amin và DNA tương đồng. Các enzym mà hành động về tinh bột và dẫn xuất của nó được phân loại thành nhiều của các gia đình và có thể được xem trên trang web của CAZY (: //afmb.cnrs-mrs.fr/ CAZY /) (Coutinho và Henrissat, 1999). Hiện nay, trang web này bao gồm 91 gia đình riêng biệt, mà gia đình 4, 13, 31, 57, 70 và 77 bao gồm enzyme mà hiển thị hoạt động trên tinh bột hoặc dẫn xuất của nó. Mặc dù mỗi gia đình bao gồm các enzyme mà hiển thị thứ tự tương tự và có chứa một số dư lượng bảo tồn các axit amin mà cụ thể đối với họ, mỗi gia đình cũng bao gồm một số phản ứng khác nhau specificities. Điều này cũng được nhìn thấy với các gia đình có chứa các enzyme mà hành động trên tinh bột. Gia đình 13 bao gồm enzyme với _amylase (EC 3.2.1.1), pullulanase (EC 3.2.1.41), isoamylase (EC 3.2.1.68), glucan phân nhánh (EC 2.4.1.18) và cyclodextrin glycosyltransferase (EC 2.4.1.19) hoạt động. Gia đình 57 posseses _-amylase (EC 3.2.1.1), _-hoá (EC 3.2.1.22) và các hoạt động 4-_-glucanotransferase (EC 2.4.1.-), trong khi gia đình 77 bao gồm amylomaltase và 4-_-glucoantransferase hoạt động (EC 2.4.1.-). Gia đình 4 có nhiều hoạt động bao gồm maltose-6-phosphate glucosidase (EC 3.2.1.122), _-glucosidase (EC 3.2.1.20), _-hoá (EC 3.2.1.22), 6-phospho-_-glucosidase (EC 3.2.1.86) và _-glucuronidase (EC 3.2.1.139). Gia đình 31 bao gồm sau hoạt động - glucosidase (EC 3.2.1.20); glucoamylase (EC 3.2.1.3); sucrase-isomaltase (EC 3.2.1.48) (EC 3.2.1.10); _-xylosidase (EC 3.2.1.-); _-glucan lyase (EC 4.2.2.13); isomaltosyltransferase (EC 2.4.1.-) (A5) Hình. Enzym thủy phân tinh bột và dẫn xuất của nó. Vì lý do rõ ràng không phải tất cả các hoạt động và các sản phẩm được bao gồm2. bột hạt làm giảm đi enzyme Tính chất tinh thể bán của tinh bột, một ungelatinised tinh bột hạt tiêu hóa chậm nhiều hơn của tinh bột hydrolysing enzyme hơn một hạt gelatinized hoặc một giải pháp tinh bột. Trong quá trình thủy phân một loạt các khác nhau morphologies có thể được quan sát thấy, mà phạm vi từ rỗ nhỏ lỗ, vỏ hình thành, và xói mòn bề mặt. Các chế độ của enzym suy thoái là phụ thuộc cả hai trên cácEnzym để điều trị ở nhiệt độ tiểu gelatinization dẫn tới xốp tinh bột. Tinh bột xốp thu hút rất nhiều sự chú ý cho sự hấp thụ của nó và bảo vệ các khả năng trong nhiều ứng dụng thực phẩm. Đặc trưng:• Α-amylase hoặc amyloglucosidase hành động trên tinh bột ngô được nghiên cứu• Dán và nhiệt thuộc tính của tinh bột xốp phụ thuộc vào men tiêu hóa được sử dụng• Xốp tinh bột là dễ bị enzyme tiêu hóa Bằng cách sử dụng enzym: nấm α-amylase (AM) hoặc amyloglucosidase (AMG)Α-Amylase có thể hydrolyze các trái phiếu α-glucosidic (1→4) của tinh bột trong một hành động endo. Thủy phân xảy ra một cách ngẫu nhiên tại bất kỳ (1→4)-các liên kết trong chuỗi tinh bột để nhanh chóng giảm kích thước phân tử của tinh bột và độ nhớt của các giải pháp tinh bột trong dán. Amyloglucosidase là một loại enzyme exo tác catalyzes thủy phân α-D-(1→4) và α - D-(1→6)-các liên kết từ phòng không giảm đầu của chuỗi tinh bột. Nhiều nhà nghiên cứu đã điều tra các enzym thủy phân tinh bột ngũ cốc, rễ, củ và đậu trong điều khoản của enzym hấp phụ, mô hình hành động, mức độ thủy phân, mức độ crystallinity và thủy phân các sản phẩm Hình. Hạt tinh bột khoai tây trước khi (trái) và sau khi suy thoái bởi amylase từ Paenibacillus granivorans (giữa) và Microbaterium aureum (bên phải). (A5)• Phương phápPhương pháp 1: Thử nghiệm sơ bộ được thực hiện để tối ưu hóa các phản ứng enzym (số lượng tinh bột và pH), và độ pH 4.0 được chọn để phản ứng AMG và pH 6.0 trong trường hợp sửa đổi AM. Số lượng của các enzym được dựa trên thử nghiệm trước đó, nơi số lượng các men tiêu hóa cần thiết để hydrolyze 50% của tinh bột (15%, w/v) tại 95ºC cho 10 phút đã được lựa chọn.Tinh bột (5.0 g) đã bị đình chỉ trong 25 mL 20mM NaH2PO4 đệm ở pH 6.0 hoặc trong natri axetat đệm ở pH 4.0, những mẫu tinh bột được gọi là kiểm soát-6 hoặc kiểm soát-4, tương ứng. Cho việc thu thập các tinh bột được điều trị enzym, enzyme (4 U AMG /g tinh bột) và 5 U AM /g tinh bột được thêm vào để đình chỉ tinh bột. Mẫu được giữ trong một bồn tắm nước lắc (50 rpm) tại 50 ºC cho 24 giờ. Sau đó, 50 mL nước được bổ sung và đình chỉ được homogenized. Mẫu đã ly cho 15 phút ở 7, 000 × g và 4 ºC. Tinh bột được rửa sạch một lần nữa và ly lúc các điều kiện tương tự như trước. Supernatants được gộp lại với nhau và luộc trong một nước tắm cho 10 phút để hủy kích hoạt các enzym trước khi bất kỳ phân tích thêm (hydrat hóa tài sản và iốt ràng buộc giá trị). Trầm tích chứa tinh bột đông khô và lưu giữ tại - 25ºC cho phân tích hơn nữa nhiệt, hóa sinh và microstructural. Bốn lô đã được chuẩn bị cho mỗi lần điều trị (A2)Phương pháp 2: Enzyme phân loại tinh bột đã đạt được bằng cách sử dụng enzym α-amylase (sứ tuyến tụy amylase). 40% tinh bột bùn đã được chuẩn bị bằng cách thêm 40gm của tinh bột đến 100ml nước cất, và men tiêu hóa (100µl) đã được bổ sung. Các mẫu đã được cho phép để đứng ở nhiệt độ phòng trong 6giờ. Các bình được sau đó giữ trong các vườn ươm tại 50oC cho 3h. Sau khi ủ bệnh, supernatant decanted và tinh bột được lọc và khô trong lò ở 500 C. (A31)3. tinh bột transferasesα 1,4-Glucanotransferases catalyse the cleavage of α-1,4 glucosidic bonds and the transfer of the newly formed reducing end group (donor) to a non-reducing saccharide unit (acceptor) with the formation of a new α -1,4 glucosidic bond. Donor and acceptor may originate from the same type of molecule or from different types of molecules. Several action patterns may be distinguished. Firstly, a single low molar mass maltooligosaccharide molecule may act both as donor and acceptor. In this case, cyclic saccharides are formed. Familiar examples are the cyclodextrins (CDs) with 6, 7, or 8 glucose units in the ring, which are formed by cyclodextrin glucosyltransferase. The net result of this type of activity is a decrease in the average molar mass. CDs are prepared by incubating a starch liquefact of DE < 10 with CGT-ase from Bacillus macerans (Riisgaard, 1990) or from thermostable microorganisms like Thermoanaerobacter species (Starnes, 1990). By addition of a complexing solvent, a crystalline inclusion complex is formed that can be separated from the mother liquor and refined by redissolution in water and recrystallisation. In a non-solvent process, the linear malto-oligosaccharides are degraded by amylolysis and cyclodextrin is recovered by partial evaporation and crystallisation. Like amylose, CDs have the ability to form crystalline complexes with a number of inclusion compounds. CDs have been widely explored as drug and flavour carriers (Szejtli, 1998). A novel development of randomly methylated α -CD is its use as an aid in emulsion polymerisation, e.g. in the surfactant-free production of polystyrene and polymethylmethacrylate latex particles in aqueous media (Storsberg et al., 2003). A different situation arises when the donor is transferred either to a different acceptor molecule or to a different side chain on the same molecule, e.g., in amylopectin. An interesting example is the so-called disproportioning enzyme or D-enzyme, also named amylomaltase because it catalyses the transfer of maltose from starch to glucose. A well known source of this enzyme is the potato, but a thermostable amylomaltase has also been isolated from Thermus thermophilus. Limited action of this enzyme on gelatinised starch leads to the progressive disappearance of amylose and the formation of amylopectin with a broader chain-length distribution. During this process the granular remnants dissolve completely and a low viscous molecular solution is obtained with a shift in iodine absorption maximum to lower wavelengths. Interestingly, these solutions form turbid rubber-like gels with a relatively high modulus on cooling at concentrations as low as 3%, which melt again on heating to c. 70oC. Amylomaltase-modified starch is a potential gelatin replacer in applications where gel transparency is not an issue. At higher conversions with this enzyme, cyclisation reactions on both linear and branched molecules occur, leading to relatively high molar mass starch products with a limited tendency to retrograde (Takaha et al., 1996, 1997). A third situation arises when a different linkage type is formed during the transfer reaction. The action of starch branching enzyme (SBE) involves breaking of an -1,4-linkage and the concomitant formation of an -1,6-linkage. Thermostable branching enzymes have been isolated from a limited number of sources, e.g., Bacillus stearothermophilus.
The main effect is an overall reduction of amylopectin chain length, thereby reducing the propensity of starch to retrograde and increasing the solubility of starch in water. The fact that this action also results in the elimination of amylose and is not accompanied by the formation of maltose as a by-product makes SBE more useful than α-amylase. Involvement of a newly formed reducing end group into an α-1,6 linkage on the same molecule will also lead to the formation of cyclic molecules (Takata et al., 1996, 1997). (A5)

Fig1. Schematic representation of the reactions catalyzed hydrolases and transferases acting on starch. (M4)
3.1. Starch Branching Enzymes
The super-cluster structure of amylopectin (Gallant et al., 1997) might have evolved as a fitting strategy for plant survival and must be accomplished by well-refined regulation of a network of numerous enzyme actions. The fine structure of amylopectin is distinct from that of glycogen in animals and bacteria in that glycogen is randomly branched, the branches are more numerous, and the chains are shorter compared with amylopectin
Method :
Assay of starch Branching Enzymes.
The basis of the assay