CN108732110A - A kind of analysis method of banana stalk chemical analysis - Google Patents

A kind of analysis method of banana stalk chemical analysis Download PDF

Info

Publication number
CN108732110A
CN108732110A CN201810884810.6A CN201810884810A CN108732110A CN 108732110 A CN108732110 A CN 108732110A CN 201810884810 A CN201810884810 A CN 201810884810A CN 108732110 A CN108732110 A CN 108732110A
Authority
CN
China
Prior art keywords
sample
banana stalk
chemical analysis
supernatant
analysis
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201810884810.6A
Other languages
Chinese (zh)
Inventor
唐粉玲
李敬阳
王安邦
林妃
李艳霞
李羽佳
王甲水
许奕
魏卿
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Haikou Experimental Station of Chinese Academy of Tropical Agricultural Sciences
Original Assignee
Haikou Experimental Station of Chinese Academy of Tropical Agricultural Sciences
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Haikou Experimental Station of Chinese Academy of Tropical Agricultural Sciences filed Critical Haikou Experimental Station of Chinese Academy of Tropical Agricultural Sciences
Priority to CN201810884810.6A priority Critical patent/CN108732110A/en
Publication of CN108732110A publication Critical patent/CN108732110A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Sampling And Sample Adjustment (AREA)

Abstract

The invention discloses a kind of analysis methods of banana stalk chemical analysis, include the following steps:Material prepares, rubber banana stalk sample is put into pond, it is rinsed by tap water, chopping, it is dry in aeration cabinet, record moisture, sample is crushed with pulverizer, it is sieved with sieve, obtain Sample A, and Sample A is preserved at room temperature for use, buck, Sample A is ground into sieving, extraction obtains sample B, again through vacuum filter, and it is dry in aeration cabinet, soluble sugar measures, sample B is dried to weight, mixing, weigh dry weight sample, appropriate phosphate buffer is added fully to mill, it shifts in centrifuge tube, constant volume, mixing sample, centrifugal treating.The present invention improves the utilization rate of sample, is conducive to control experimental variable, improves the reliability of analysis result so that the analysis result of banana stalk chemical analysis is relatively reliable, is conducive to the utilization of banana stalk, rationally utilizes resource.

Description

A kind of analysis method of banana stalk chemical analysis
Technical field
The present invention relates to the analysis technical field of banana stalk chemical analysis more particularly to a kind of banana stalk chemical analysis Analysis method.
Background technology
Banana all one's life one inferior fruit of knot, is left a large amount of agricultural residues, these residues cause pest and disease damage propagation and environment Pollution.It can be converted into ethyl alcohol using the lignocellulosic extracted in banana residue as bioenergy, or carry out resource Change and utilizes(Such as feed, fertilizer), reach improvement agricultural environment, improve the purpose of land output.Accurate analysis banana stalk is thin Cell wall composition determines that its different purposes is all particularly important for precisely identifying banana variety, existing analysis method, Bu Nengzhun The chemical composition of true analysis banana stalk, it has not been convenient to which banana stalk recycles, so now proposing a kind of banana stalk chemistry The analysis method of composition.
Invention content
Technical problems based on background technology, the present invention propose a kind of analysis side of banana stalk chemical analysis Method.
A kind of analysis method of banana stalk chemical analysis proposed by the present invention, includes the following steps:
S1:Material prepares, and banana stalk sample is put into pond, is rinsed by tap water, chopping, is done in aeration cabinet It is dry, moisture is recorded, sample is crushed with pulverizer, sieved with sieve, obtains Sample A, and Sample A is preserved at room temperature and is waited for With;
S2:Sample A is ground sieving by buck, and extraction obtains sample B, then through vacuum filter, and is done in aeration cabinet It is dry;
S3:Soluble sugar measures, and sample B is dried to weight, mixing weighs dry weight sample, and appropriate phosphate buffer is added and fills Divide and mill, shift in centrifuge tube, constant volume, mixing sample, centrifugal treating, collects supernatant in centrifuge tube, precipitate again successively With phosphate buffer and distilled water flushing, precipitate C is obtained, collects all supernatants in centrifuge tube, constant volume, colorimetric method for determining five Carbon sugar, hexose, record data;
S4:Liposoluble substance is removed, chloroform-methanol, vibration processing are added in precipitate C, centrifugal treating removes supernatant, sinks Shallow lake is washed 1 time with 5.0ml methanol successively again, and 5ml acetone is washed 1 time, finally with distillation washing 1 time, is removed supernatant, is precipitated D;
S5:Starch and assay are extracted, DMSO-H is added in precipitating in D2O is uniformly mixed, and concussion processing after centrifugation, is received Collect supernatant, precipitation uses DMSO- H successively again2O and distilled water are rinsed respectively, are collected all supernatants, are precipitated E, by supernatant constant volume, distilled water dialysis is collected liquid after all dialysis, is sampled, colorimetric method for determining pentose, hexose, note Record data;
S6:KOH is added in precipitating in hemicellulose and colorimetric method assay in E, concussion processing, centrifugal treating collects supernatant Liquid, precipitation use KOH and distilled water flushing, collect all supernatants successively again, obtain precipitation F, constant volume, five carbon of colorimetric method for determining Sugar, hexose record data;
S7:H will be added in precipitation F in the insoluble hemicellulose of alkali and total fiber element and assay2SO4, mixing, concussion processing, Distilled water constant volume, after cooling, centrifugal treating collects all supernatants, sampling, and colorimetric method for determining pentose, hexose record number According to.
Preferably, the temperature of aeration cabinet is 45 DEG C in the S1, and drying time is 3-5 days, and the aperture of sieve is 0.5mm。
Preferably, it is 40 mesh that grit number is crossed in the S2, and the temperature of wind drying box is 40 DEG C, and drying to moisture is less than 10%。
Preferably, it is 40 mesh that grit number is crossed in the S2, and the temperature of wind drying box is 40 DEG C, and drying to moisture is less than 10%。
Preferably, the centrifugal treating carries out under 3000g rotating speeds, centrifugation time 5min.
Preferably, in described S4, S5, S6 and S7, vibration processing 150rpm in 25 °C of shaking tables is carried out, The time of vibration processing is 1 hour in S4, S6 and S7, and the time of vibration processing is 12 hours in S5.
Having the beneficial effect that in the present invention:
Step of the present invention is close, improves the utilization rate of sample, is conducive to control experimental variable, improves the reliability of analysis result, So that the analysis result of banana stalk chemical analysis is relatively reliable, be conducive to the utilization of banana stalk, rationally utilize resource.
Description of the drawings
Fig. 1 is a kind of flow diagram of the analysis method of banana stalk chemical analysis proposed by the present invention.
Specific implementation mode
Following will be combined with the drawings in the embodiments of the present invention, and technical solution in the embodiment of the present invention carries out clear, complete Site preparation describes, it is clear that described embodiments are only a part of the embodiments of the present invention, instead of all the embodiments.
Referring to Fig.1, a kind of analysis method of banana stalk chemical analysis, includes the following steps:
S1:Material prepares, and rubber sample is put into pond, is rinsed by tap water, chopping, in aeration cabinet at 45 DEG C It is 3-5 days dry, moisture is recorded, sample is crushed with pulverizer, is sieved with sieve 0.5mm sieve pores, obtains Sample A, and will examination Sample A is preserved for use at room temperature;
S2:Buck grinds Sample A, crosses 40 mesh sieve, and extraction obtains sample B, then through vacuum filter, and in aeration-drying It is dry in case, it is dried to moisture at 40 DEG C and is less than 10%;
S3:Soluble sugar measures, and sample B is dried to weight under the conditions of 65 °C, mixing weighs 0.1000 g dry weight samples Product, the 0.5M phosphate buffers that appropriate pH=7.0 are added fully are milled, and are shifted in 15 ml centrifuge tubes, constant volume to 10.0ml, are mixed Even sample, 3000g centrifuge 5 min, collect supernatant in 50 ml centrifuge tubes, precipitation is washed with 5.0 ml buffer successively again 2 times, 5.0 ml distillations washing 2 times obtains precipitate C, collects all supernatants in 50 ml centrifuge tubes, constant volume, colorimetric method is surveyed Determine pentose, hexose, records data;
S4:Liposoluble substance is removed, 5.0 ml chloroform-methanols are added in precipitate C(1:1 v/v), in 25 °C of shaking tables 150rpm vibrates 1h, and 3000g centrifuges 5min, removes supernatant, and precipitation is washed 1 time with 5.0ml methanol successively again, and 5ml acetone is washed 1 time, finally with 5.0 ml distillations washing 1 time, supernatant is removed, precipitation D is obtained;
S5:Starch and assay are extracted, 5.0 ml DMSO-H are added in D in precipitating2O(9:1 v/v), it is uniformly mixed, concussion Processing, in 25 °C of shaking tables, 150rpm gently shaken overnights(12h), after centrifugation, supernatant is collected, is precipitated again successively with 5.0 ml DMSO- H2O is washed 2 times, and 5.0 ml distillations washing 3 times collects all supernatants, obtains precipitation E, supernatant is settled to 30.0ml, distilled water dialysis 48h(Bag filter 8000-14000Da every two hours changes a water), collect liquid after all dialysis Body is settled to 70.0ml in 100ml graduated cylinders, samples, colorimetric method for determining pentose, hexose;
S6:5.0 ml 4M KOH are added in precipitating in hemicellulose and colorimetric method assay in E(Include 1 mg/ml's NaHB4), 150rpm vibrates 1h in 25 °C of shaking tables, and 3000g centrifuges 5min, collects supernatant, precipitates again successively with 5.0 ml 4M KOH are washed 1 time, and 5 ml distillations washing 2 times collects all supernatants, obtains precipitation F, constant volume, five carbon of colorimetric method for determining Sugar, hexose;
S7:3.0 ml 67% (v/v) H will be added in precipitation F in the insoluble hemicellulose of alkali and total fiber element and assay2SO4, Mixing, 150rpm vibrates 1h in 25 °C of shaking tables, and distilled water is settled to 10.0ml(Terminate hydrolysis), after cooling, 3000g from Heart 5min collects all supernatants, sampling, colorimetric method for determining pentose, hexose, pentose be the insoluble hemicellulose of alkali, six Carbon sugar is cellulose.
The several representative banana variety compositions of table 1
The foregoing is only a preferred embodiment of the present invention, but scope of protection of the present invention is not limited thereto, and it is any Those familiar with the art in the technical scope disclosed by the present invention, according to the technique and scheme of the present invention and its invents Design is subject to equivalent substitution or change, should be covered by the protection scope of the present invention.

Claims (6)

1. a kind of analysis method of banana stalk chemical analysis, which is characterized in that include the following steps:
S1:Material prepares, and banana stalk sample is put into pond, is rinsed by tap water, chopping, is done in aeration cabinet It is dry, moisture is recorded, sample is crushed with pulverizer, sieved with sieve, obtains Sample A, and Sample A is preserved at room temperature and is waited for With;
S2:Sample A is ground sieving by buck, and extraction obtains sample B, then through vacuum filter, and is done in aeration cabinet It is dry;
S3:Soluble sugar measures, and sample B is dried to weight, mixing weighs dry weight sample, and appropriate phosphate buffer is added and fills Divide and mill, shift in centrifuge tube, constant volume, mixing sample, centrifugal treating, collects supernatant in centrifuge tube, precipitate again successively With phosphate buffer and distilled water flushing, precipitate C is obtained, collects all supernatants in centrifuge tube, constant volume, colorimetric method for determining five Carbon sugar, hexose, record data;
S4:Liposoluble substance is removed, chloroform-methanol, vibration processing are added in precipitate C, centrifugal treating removes supernatant, sinks Shallow lake is washed 1 time with 5.0ml methanol successively again, and 5ml acetone is washed 1 time, finally with distillation washing 1 time, is removed supernatant, is precipitated D;
S5:Starch and assay are extracted, DMSO-H is added in precipitating in D2O is uniformly mixed, and concussion processing after centrifugation, is collected Supernatant, precipitation use DMSO- H successively again2O and distilled water are rinsed respectively, collect all supernatants, obtain precipitation E, By supernatant constant volume, distilled water dialysis is collected liquid after all dialysis, is sampled, colorimetric method for determining pentose, hexose, record Data;
S6:KOH is added in precipitating in hemicellulose and colorimetric method assay in E, concussion processing, centrifugal treating collects supernatant Liquid, precipitation use KOH and distilled water flushing, collect all supernatants successively again, obtain precipitation F, constant volume, five carbon of colorimetric method for determining Sugar, hexose record data;
S7:H will be added in precipitation F in the insoluble hemicellulose of alkali and total fiber element and assay2SO4, mixing, concussion processing, steaming Distilled water constant volume, after cooling, centrifugal treating collects all supernatants, sampling, and colorimetric method for determining pentose, hexose record number According to.
2. a kind of analysis method of banana stalk chemical analysis according to claim 1, which is characterized in that lead in the S1 The temperature of wind drying box is 45 DEG C, and drying time is 3-5 days, and the aperture of sieve is 0.5mm.
3. a kind of analysis method of banana stalk chemical analysis according to claim 1, which is characterized in that mistake in the S2 Grit number is 40 mesh, and the temperature of wind drying box is 40 DEG C, and drying to moisture is less than 10%.
4. a kind of analysis method of banana stalk chemical analysis according to claim 1, which is characterized in that the S3 pilot scales The drying temperature of sample B is 65 °C, and phosphate buffer is the 0.5M phosphate buffers of pH=7.0.
5. a kind of analysis method of banana stalk chemical analysis according to claim 1, which is characterized in that at the centrifugation Reason carries out under 3000g rotating speeds, centrifugation time 5min.
6. a kind of analysis method of banana stalk chemical analysis according to claim 1, which is characterized in that the S4, S5, In S6 and S7, vibration processing 150rpm in 25 °C of shaking tables is carried out, in S4, S6 and S7 the time of vibration processing be 1 hour, the time of vibration processing was 12 hours in S5.
CN201810884810.6A 2018-08-06 2018-08-06 A kind of analysis method of banana stalk chemical analysis Pending CN108732110A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810884810.6A CN108732110A (en) 2018-08-06 2018-08-06 A kind of analysis method of banana stalk chemical analysis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810884810.6A CN108732110A (en) 2018-08-06 2018-08-06 A kind of analysis method of banana stalk chemical analysis

Publications (1)

Publication Number Publication Date
CN108732110A true CN108732110A (en) 2018-11-02

Family

ID=63942240

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810884810.6A Pending CN108732110A (en) 2018-08-06 2018-08-06 A kind of analysis method of banana stalk chemical analysis

Country Status (1)

Country Link
CN (1) CN108732110A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113340764A (en) * 2021-06-15 2021-09-03 中国林业科学研究院林产化学工业研究所 Method for analyzing fiber fraction and fiber bundle content of plant fibers

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101187068A (en) * 2007-02-15 2008-05-28 吴苏明 Japanese banana fiber and its preparation method and uses

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101187068A (en) * 2007-02-15 2008-05-28 吴苏明 Japanese banana fiber and its preparation method and uses

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
H. S. SHANTHA,ET AL.: "Accumulation of Starch in Banana Pseudostem and Fruit", 《JOURNAL OF FOOD SCIENCE》 *
LI KUN,ET AL.: "ANALYSIS OF THE CHEMICAL COMPOSITION AND MORPHOLOGICAL STRUCTURE OF BANANA PSEUDO-STEM", 《BIORESOURCES》 *
PCFLI4: "比色法测定可溶性糖、果胶、半纤维素、纤维素含量", 《HTTP://WWW.DOCIN.COM/P-701242522.HTML》 *
吴莲蓉: "油菜茎秆生化成分和倒伏相关性研究", 《中国优秀硕士学位论文全文数据库 农业科技辑》 *
郑丽丽 等: "香蕉茎秆废弃物综合利用研究现状与分析 ", 《热带农业科学》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113340764A (en) * 2021-06-15 2021-09-03 中国林业科学研究院林产化学工业研究所 Method for analyzing fiber fraction and fiber bundle content of plant fibers

Similar Documents

Publication Publication Date Title
CN103868778B (en) The measuring method of herbaceous plant content of lignin
Muhammad et al. Survey of wheat straw stem characteristics for enhanced resistance to lodging
CN104655784A (en) Method for determining lignocelluloses component content of plant straw
CN103193522B (en) Vegetable seedling breeding matrix material made of hickory cattail husk and preparation method for vegetable seedling breeding matrix material
CN104169429A (en) Improved pre-soaking process for biomass conversion
CN105646728B (en) A kind of honey comb polyoses extract and preparation method thereof
CN108904607B (en) Method for extracting polyphenols from oil peony seed shells
CN108732110A (en) A kind of analysis method of banana stalk chemical analysis
CN103694366A (en) Preparation method of high-content lentinan
CN109232760A (en) Phellinus protect liver polysaccharide PPB-2 and preparation method thereof
CN107281258A (en) A kind of beans taro leaf flavonoid extract and its preparation method and application
CN105385631A (en) Lignocellulos substance high-efficiency degrading bacterium M1 and application thereof
CN104844721B (en) Extraction and separation method of Agrocybe aegirit polysaccharides
CN103308614A (en) High performance liquid chromatography method for simultaneously detecting contents of melanin and inosinic acid in chicken of silky fowl
CN106093240A (en) A kind of fast-growing Radix Astragali and the discrimination method of the wild Radix Astragali
KR101152104B1 (en) Methods for producing red ginseng extracts with improved sweetness and production yield
CN105385629A (en) Lignocellulos substance high-efficiency degrading bacterium M2 and application thereof
Piperno A few kernels short of a cob: on the Staller and Thompson late entry scenario for the introduction of maize into northern South America
CN109900531A (en) A kind of extracting method of coral lipid
CN107082822B (en) A kind of mango processing byproduct polysaccharide takes off albumen and discoloration method
Mason et al. The concentration of solutes in sap and tissue, and the estimation of bound water
CN106769278B (en) A kind of cell block reagent preparation box and preparation method thereof
CN105462875A (en) Strain L252 capable of efficiently degrading lignocellulose substances and application of strain
CN105274038A (en) Lignocellulose substance efficient degradation bacterium II83 and application thereof
Buta An Evaluation of Oxalate Content in Cassava Roots and Sweet Potato Tubers in Areka, Ethiopia

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20181102